Time
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Page Name
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Author of this revision
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Description
|
Flags
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2024-06-14 17:17
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Chromosomal aberrations in etiology of neoplasms
|
Tereza Bergendyová
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/* Source */
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|
2024-06-14 17:17
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Chromosomal aberrations in etiology of neoplasms
|
Tereza Bergendyová
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edited citations
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|
2024-06-01 09:32
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Genetics of Ig, B and T receptors
|
Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:32
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Genetic heterogeneity and protein polymorphisms
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Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:32
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Genetic control of antibody production
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Karvasa
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Added categories, Karvasa
|
|
2024-06-01 09:31
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Genetic causes of the aging process and death
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Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:31
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Genetic Polymorphisms
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Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:30
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Gene Structure and Function
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Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:30
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Gene-environment interactions
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Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:29
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Fabry disease
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Karvasa
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Added categories, Karvasa
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|
2024-06-01 09:27
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Euchromatin
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Karvasa
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Added categories, Karvasa
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|
2024-05-30 22:18
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Dihybridism- close up
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Karvasa
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Added categories and links Karvasa
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2024-05-30 21:03
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Defects of Hemoglobin
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Karvasa
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Added categories, Karvasa
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|
2024-05-30 19:24
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Cell cycle and its regulation
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Karvasa
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Added categories, Karvasa
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2024-05-22 14:14
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Genetically modified foods
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Jakub Jan Kvašňák
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/* Links */
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2024-05-19 09:00
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Causes of chromosomal aberrations
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Karvasa
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Added categories, deleted czech text that was duplicated, karvasa
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|
2024-05-19 08:58
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Cancer Cells Characteristics
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Karvasa
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Added categories, Karvasa
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|
2024-05-10 20:46
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Cell membrane - structure and function
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Mkvas1
|
|
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2024-05-10 20:46
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Cell division – mitosis and meiosis
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Mkvas1
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|
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2024-05-10 20:45
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Cell division – mitosis and meiosis
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Mkvas1
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|
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2024-04-25 16:09
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Tumor suppressor gene
|
Jakub Jan Kvašňák
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/* General */
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2024-04-25 16:09
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Tumor suppressor gene
|
Jakub Jan Kvašňák
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/* Source */
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2024-04-25 16:08
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Tumor suppressor gene
|
Jakub Jan Kvašňák
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/* p53 */
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2024-04-25 16:08
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Tumor suppressor gene
|
Jakub Jan Kvašňák
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/* pRB */
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2024-04-23 19:51
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Mitochondria
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Jakub Jan Kvašňák
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2024-04-11 21:42
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Gametogeneze
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Arya Vinay Pawar
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|
me
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2024-04-11 21:09
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Gametogeneze
|
Arya Vinay Pawar
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Embryonic Origin of Spermatogonia and Oogonia
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|
2024-04-06 14:13
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Cell cycle and its regulation
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janaty kondos
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Summary of Amit's notes
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2024-04-06 14:07
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Cell division – mitosis and meiosis
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janaty kondos
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Summary of Amit's notes
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2024-04-06 13:09
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Cell membrane - structure and function
|
janaty kondos
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|
me
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2024-04-06 12:19
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Cell membrane - structure and function
|
janaty kondos
|
Created page with "'''Cell Membrane – Structure and Function''' All eukaryotic cells are enveloped by a limiting membrane composed of: • Lipids - Phospholipids and Cholesterol, glycolipids • Proteins • Chains of oligosaccharides (small number of simple sugars, monosaccharides) linked to phospholipid and protein molecules. '''Characteristic of biological membrane :''' • Asymmetric • Fluid Mosaic Membranes exhibit a thickness ranging from 7.5 to 10 nm, rendering them vi..."
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2024-03-18 17:15
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Allelic heterogeneity
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Nandini
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|
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2024-03-18 17:11
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Alkaptonuria
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Nandini
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|
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2024-03-18 16:58
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Additive model of polygenic inheritance
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Nandini
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2024-02-14 17:36
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Burton's agammaglobulinemia
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Bryce Seguin
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|
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2024-02-07 09:58
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Chromosomal determination of sex
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Paraskevi Chatziloizou
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Added links
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2024-02-05 15:45
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Antigen
|
Jakub Jan Kvašňák
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|
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2024-02-03 14:40
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Cri du chat syndrome
|
Jakub Jan Kvašňák
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|
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2024-02-03 14:40
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Cri du chat syndrome
|
Jakub Jan Kvašňák
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|
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2024-02-03 14:37
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Cri du chat syndrome
|
Jakub Jan Kvašňák
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2024-02-03 14:31
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Cri du chat syndrome
|
Jakub Jan Kvašňák
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/* Used literature */
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2024-02-03 14:28
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Cri du chat syndrome
|
Jakub Jan Kvašňák
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/* References */ added categories
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2024-01-26 22:17
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Cell cooperation in the B immune response
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Jakub Jan Kvašňák
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/* Links */ fixed category, translated citation
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2024-01-23 14:04
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Mitochondrial diseases / Respiratory chain enzyme deficiency
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Jakub Jan Kvašňák
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/* Used literature */
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2024-01-23 14:04
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Mitochondrial diseases / Respiratory chain enzyme deficiency
|
Jakub Jan Kvašňák
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/* Used literature */
|
|
2024-01-23 14:01
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Mitochondrial diseases / Respiratory chain enzyme deficiency
|
Jakub Jan Kvašňák
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/* Used literature */
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2024-01-23 14:01
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Mitochondrial diseases / Respiratory chain enzyme deficiency
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Jakub Jan Kvašňák
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/* Used literature */
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2024-01-23 14:00
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Mitochondrial diseases / Respiratory chain enzyme deficiency
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Jakub Jan Kvašňák
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/* Used literature */
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|
2024-01-23 14:00
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Mitochondrial diseases / Respiratory chain enzyme deficiency
|
Jakub Jan Kvašňák
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/* Used literature */
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|
2024-01-23 13:58
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Mitochondrial diseases / Respiratory chain enzyme deficiency
|
Jakub Jan Kvašňák
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fixing and actually translating citations and categories
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|
2024-01-23 13:41
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Inhibitors (genetics)
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Jakub Jan Kvašňák
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/* References */ fixed citation
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|
2024-01-22 16:35
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Biological characteristics of tumors
|
Tereza Filipová
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Editace a přidání kategorií.
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|
2024-01-22 15:13
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Control of gene expression and proteosynthesis in eukaryotes
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Jakub Jan Kvašňák
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/* Resources */ fixed category typo
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2024-01-21 18:43
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Autoimunitní lymfoproliferativní syndrom
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Tereza Filipová
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Editace a přidání kategorie.
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2024-01-19 17:37
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Apoptosis and clinical consequences of its dysregulation
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Cateducated
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added categories
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2024-01-18 16:06
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Amplification and expression of the isolated gene in the host cell
|
Tereza Filipová
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Editace a přidání kategorií.
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2024-01-18 12:02
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Cowden's syndrome
|
SatPet
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|
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2024-01-18 09:08
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Alport's syndrome
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SatPet
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|
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2024-01-17 18:28
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Li-Fraumeni syndrome
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Cateducated
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added category
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2024-01-17 18:28
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Meiosis, its regulation and disturbances
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Cateducated
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added category
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|
2024-01-17 18:24
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Mental retardation
|
Cateducated
|
added categories
|
|
2024-01-17 18:21
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Metabolic osteopathies
|
Cateducated
|
added categories
|
|
2024-01-17 17:40
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Allelic heterogeneity
|
Tereza Filipová
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Přidání kategorie.
|
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2024-01-16 21:58
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Hemoglobinopathy
|
Cateducated
|
added categories
|
|
2024-01-16 21:39
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DNA viruses
|
Cateducated
|
added category
|
|
2024-01-16 21:39
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DNA fingerprinting
|
Cateducated
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added category
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|
2024-01-16 21:39
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DNA (nucleic acid)
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Cateducated
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added category
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|
2024-01-16 21:39
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DNA Sequencing
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Cateducated
|
added categories
|
|
2024-01-16 17:27
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A sublethal gene
|
Tereza Filipová
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Editace a přidání kategorie.
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2024-01-15 20:47
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Biochemistry of genetic engineering
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Cateducated
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added category
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|
2024-01-15 20:43
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Bacterial cell wall
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Cateducated
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added category
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2024-01-15 20:40
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Automatic analysis of 2D polyacrylamide gels in the diagnosis of DNA polymorphisms
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Cateducated
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added category
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2024-01-15 20:39
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Autophagy, Hayflick's limit, telomerase
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Cateducated
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added category
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2024-01-15 20:38
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Autosomally inherited agammaglobulinemia
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Cateducated
|
added categories
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|
2024-01-15 20:37
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Autosome
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Cateducated
|
added category
|
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2024-01-15 20:28
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Autoimmune lymphoproliferative syndrome
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Cateducated
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added categories
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2024-01-15 15:16
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DsDNA
|
Cateducated
|
added categories
|
|
2024-01-14 21:40
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DiGeorge syndrome
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Cateducated
|
added category
|
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2024-01-14 21:39
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DiGeorge syndrome
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Cateducated
|
added categories
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|
2024-01-14 21:39
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DiGeorge syndrome
|
Cateducated
|
added categories
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2024-01-14 21:38
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DiGeorge syndrome
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Cateducated
|
added categories
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|
2024-01-14 17:27
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Phenotype
|
Michaela Rumlerová
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Přidání kategorií a editace
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2024-01-14 17:19
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Evolution
|
Michaela Rumlerová
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Úprava kategorií a citací
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2024-01-14 15:43
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Malignant
|
Michaela Rumlerová
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|
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2024-01-13 16:27
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Prion
|
Michaela Rumlerová
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Přidání kategorií
|
|
2024-01-10 19:39
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Aging of the organism
|
Beloslava Erofeeva
|
added categories
|
|
2024-01-10 19:37
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Additive model of polygenic inheritance
|
Beloslava Erofeeva
|
added categories
|
|
2024-01-10 19:04
|
Alkaptonuria
|
Beloslava Erofeeva
|
added categories
|
|
2024-01-10 18:58
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Heredity (signpost)
|
Jakub Jan Kvašňák
|
translated category
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|
2024-01-06 14:41
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Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
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|
|
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2024-01-06 14:39
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Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
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|
|
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2024-01-06 14:38
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Autosomal dominant inheritance in pedigree and experiment, examples of traits in man
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|
|
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2024-01-03 17:26
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A decision mechanism for the destruction of non-functional proteins
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|
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2024-01-03 17:24
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A decision mechanism for the destruction of non-functional proteins
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|
edited
|
|
2024-01-01 21:10
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PARK genes
|
Jakub Jan Kvašňák
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/* References */ fixed category
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|
2024-01-01 20:53
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Structural chromosomal aberrations
|
Jakub Jan Kvašňák
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/* Used literature */ fixing citations and categories
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|
2024-01-01 20:52
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Structural chromosomal aberrations
|
Jakub Jan Kvašňák
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/* Related articles */
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|
2024-01-01 20:52
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Structural chromosomal aberrations
|
Jakub Jan Kvašňák
|
/* Cri du chat syndrome */
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|
2024-01-01 20:51
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Structural chromosomal aberrations
|
Jakub Jan Kvašňák
|
/* Examples of structural aberration */ fixing image and links
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|
2023-12-24 08:17
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Human karyotype, methods of its examination
|
Viktorie Koberová
|
|
me
|
2023-12-24 08:16
|
Human karyotype, methods of its examination
|
Viktorie Koberová
|
|
me
|
2023-12-24 08:15
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Chromatin
|
Viktorie Koberová
|
|
me
|
2023-12-24 08:08
|
Euchromatin
|
Viktorie Koberová
|
Created page with "'''Euchromatin''' is a subtype of [[chromatin]] (the basic building material of chromosomes) that is not condensed. Simply put, euchromatin is handled and sections of it can undergo transcription. Condensed chromatin is termed [[heterochromatin]]."
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2023-12-24 08:04
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Hereditary immunodeficiencies
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Viktorie Koberová
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|
me
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2023-12-23 08:11
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Beckwith-Wiedemann Syndrome
|
Viktorie Koberová
|
|
me
|
2023-12-23 08:09
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Angelman Syndrome
|
Viktorie Koberová
|
|
me
|
2023-12-23 08:08
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Gametogenesis (Coursebook)
|
Viktorie Koberová
|
|
me
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2023-12-23 08:06
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Genetic linkage
|
Viktorie Koberová
|
|
me
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2023-12-22 07:26
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Dihybridism
|
Viktorie Koberová
|
|
me
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2023-12-22 07:24
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Genotype Variation, Mutations and Recombination
|
Viktorie Koberová
|
|
me
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2023-12-22 07:18
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Autosomal recessive inheritance in pedigree and experiment, examples of traits in man
|
Viktorie Koberová
|
|
me
|
2023-12-21 21:08
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APC Resistence
|
Avantika Subhash
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catergories
|
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2023-12-21 21:06
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Achondroplasia
|
Avantika Subhash
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categories
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2023-12-21 17:33
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Congenital developmental defects
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Cateducated
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added categories
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2023-12-21 17:32
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Congenital developmental defects
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Cateducated
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/* Historie */
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2023-12-21 17:31
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Congenital developmental defects of the respiratory system
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Cateducated
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added categories
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2023-12-21 17:29
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Congenital glycosylation disorders
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Cateducated
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added categories
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2023-12-21 17:26
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Congenital steep talus
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Cateducated
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added categories
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2023-12-21 17:24
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Conjugation, transformation, transduction
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Cateducated
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added categories
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2023-12-21 17:24
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Conjugation, transformation, transduction
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Cateducated
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added categories
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|
2023-12-19 21:22
|
Chromatin
|
Jakub Jan Kvašňák
|
/* Heterochromatin and Euchromatin */
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|
2023-12-19 21:22
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Chromatin
|
Jakub Jan Kvašňák
|
/* References */ fixing citations
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2023-12-19 14:19
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Osteogenesis imperfecta
|
Viktorie Koberová
|
|
me
|
2023-12-19 14:19
|
Osteogenesis imperfecta
|
Viktorie Koberová
|
|
me
|
2023-12-19 14:19
|
Osteogenesis imperfecta
|
Viktorie Koberová
|
|
me
|
2023-12-19 14:18
|
Osteogenesis imperfecta
|
Viktorie Koberová
|
|
me
|
2023-12-16 08:40
|
Bacterial cell wall
|
Viktorie Koberová
|
|
me
|
2023-12-16 08:38
|
Bacterial cell wall
|
Viktorie Koberová
|
|
me
|
2023-12-16 08:37
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Bacterial cell wall
|
Viktorie Koberová
|
|
me
|
2023-12-15 14:27
|
Bacterial cell wall
|
Viktorie Koberová
|
|
me
|
2023-12-15 14:27
|
Bacterial cell wall
|
Viktorie Koberová
|
|
me
|
2023-12-15 14:27
|
Bacterial cell wall
|
Viktorie Koberová
|
|
me
|
2023-12-09 09:19
|
Cystic Fibrosis
|
Viktorie Koberová
|
add links and pictures
|
me
|
2023-12-07 18:45
|
Mutagenesis
|
Jakub Jan Kvašňák
|
/* Resources */
|
|
2023-12-07 18:44
|
Mutagenesis
|
Jakub Jan Kvašňák
|
/* Resources */
|
|
2023-12-07 18:44
|
Mutagenesis
|
Jakub Jan Kvašňák
|
/* Resources */
|
|
2023-12-07 18:44
|
Mutagenesis
|
Jakub Jan Kvašňák
|
/* Resources */ fixing citations
|
|
2023-11-30 16:46
|
In vitro fertilization
|
Jakub Jan Kvašňák
|
/* Other methods related to IVF */
|
|
2023-11-30 16:46
|
In vitro fertilization
|
Jakub Jan Kvašňák
|
/* references */ fixing categories
|
|
2023-11-30 16:45
|
Genetic maps and their meaning
|
Jakub Jan Kvašňák
|
/* Links */ fixing categories
|
|
2023-11-30 16:45
|
Map of the human genome, HUGO, use
|
Jakub Jan Kvašňák
|
/* References */ fixing categories
|
|
2023-11-30 16:44
|
The genetic code
|
Jakub Jan Kvašňák
|
/* Links */ fixing categories
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|
2023-11-30 16:44
|
Genetic modifications
|
Jakub Jan Kvašňák
|
/* References */ fixing categories
|
|
2023-11-30 16:44
|
Evolution and speciation at the molecular level
|
Jakub Jan Kvašňák
|
/* References */ fixing categories
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|
2023-11-30 16:43
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Gene
|
Jakub Jan Kvašňák
|
/* Related articles */ fixed links and categories
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|
2023-11-30 16:42
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Manifestations of developmental toxicity
|
Jakub Jan Kvašňák
|
/* References */ fixed categories
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|
2023-11-30 11:43
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Cell
|
Gwenhwyfar Ania Gonnot
|
Added links and categories
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|
2023-11-29 12:04
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Antigen
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|
Added categories
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|
2023-11-29 12:01
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AB0 system (English)
|
Gwenhwyfar Ania Gonnot
|
Added categories
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|
2023-11-25 17:29
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Achondroplasia
|
Paraskevi Chatziloizou
|
Remove nonexistent links
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|
2023-11-24 21:20
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Non-positional Leg Defects
|
Jakub Jan Kvašňák
|
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2023-11-24 21:18
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Non-positional Leg Defects
|
Jakub Jan Kvašňák
|
/* References */
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2023-11-24 21:18
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Numerical chromosome abnormalities
|
Jakub Jan Kvašňák
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/* References */
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|
2023-11-24 21:17
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Hyperimmunoglobulinemia IgM syndrome/other types
|
Jakub Jan Kvašňák
|
/* References */
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|
2023-11-24 21:16
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Hereditary metabolic disorders/Genetic background
|
Jakub Jan Kvašňák
|
/* Source */
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2023-11-24 21:12
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Nephronophthisis
|
Jakub Jan Kvašňák
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/* Related articles */
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2023-11-24 21:07
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Congenital multiple exostoses
|
Jakub Jan Kvašňák
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/* Refrences */
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2023-11-24 21:07
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Syndromes due to aneuploidy of gonosomes
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Jakub Jan Kvašňák
|
/* Source */
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2023-11-24 21:04
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Congenital malformations of the respiratory system
|
Jakub Jan Kvašňák
|
/* Bibliography */
|
|
2023-11-24 21:02
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Meningocele
|
Jakub Jan Kvašňák
|
/* Source */
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|
2023-11-24 21:01
|
Meningocele
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 21:00
|
Meningocele
|
Jakub Jan Kvašňák
|
/* Source */
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|
2023-11-24 20:58
|
Cowden's syndrome
|
Mkvas1
|
/* External links */
|
|
2023-11-24 20:58
|
Cowden's syndrome
|
Mkvas1
|
/* External links */
|
|
2023-11-24 20:57
|
Cowden's syndrome
|
Mkvas1
|
/* External links */
|
|
2023-11-24 20:57
|
Cowden's syndrome
|
Mkvas1
|
/* External links */
|
|
2023-11-24 20:55
|
Chromosomal aberrations in etiology of neoplasms
|
Mkvas1
|
/* Source */
|
|
2023-11-24 20:55
|
Chromosomal aberrations in etiology of neoplasms
|
Mkvas1
|
/* Source */
|
|
2023-11-24 20:54
|
Chromosomal aberrations in etiology of neoplasms
|
Mkvas1
|
/* Source */
|
|
2023-11-24 20:54
|
Chromosomal aberrations in etiology of neoplasms
|
Mkvas1
|
/* Source */
|
|
2023-11-24 20:48
|
Congenital diaphragmatic hernia
|
Jakub Jan Kvašňák
|
/* Literature */
|
|
2023-11-24 20:46
|
Developmental hip dysplasia
|
Jakub Jan Kvašňák
|
/* Use literature */
|
|
2023-11-24 20:46
|
Autosomal inherited agammaglobulinemia
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-24 20:40
|
Multiple Congenital Exostoses
|
Jakub Jan Kvašňák
|
/* Refrences */
|
|
2023-11-24 20:36
|
Developmental disorders of the ear
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:36
|
Caring for a child with Down syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:36
|
Postnatal prevention of hereditary diseases
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-24 20:29
|
Examination methods of inherited metabolic disorders
|
Jakub Jan Kvašňák
|
/* Indications leading to suspicion of IMD */
|
|
2023-11-24 20:28
|
Examination methods of inherited metabolic disorders
|
Jakub Jan Kvašňák
|
/* Diagnosis of IMD */
|
|
2023-11-24 20:27
|
Bloch-Sulzberg syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:23
|
Autoimunitní lymfoproliferativní syndrom
|
Mkvas1
|
|
|
2023-11-24 20:22
|
Autoimunitní lymfoproliferativní syndrom
|
Mkvas1
|
|
|
2023-11-24 20:21
|
Autoimunitní lymfoproliferativní syndrom
|
Mkvas1
|
|
|
2023-11-24 20:18
|
Pes calcaneovalgus
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:12
|
Microdeletion syndromes
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:12
|
Prenatal screening of congenital anomalies
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:07
|
Chronic Granulomatous Disease
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 20:04
|
Metabolic osteopathy
|
Jakub Jan Kvašňák
|
|
|
2023-11-24 20:04
|
Metabolic osteopathy
|
Jakub Jan Kvašňák
|
|
|
2023-11-24 16:34
|
Congenital Heart Defects
|
Jakub Jan Kvašňák
|
/* Bibliography */
|
|
2023-11-24 16:33
|
Congenital Heart Defects
|
Jakub Jan Kvašňák
|
|
|
2023-11-24 16:32
|
Congenital Heart Defects
|
Jakub Jan Kvašňák
|
|
|
2023-11-24 16:30
|
Hereditary osteo-onychodysplasia
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-24 16:30
|
Congenital deformities of the auricle
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-24 16:29
|
Peroxisomal leukodystrophy
|
Jakub Jan Kvašňák
|
/* Reference */
|
|
2023-11-24 16:29
|
Clubfoot (congenital talipes equinovarus)
|
Jakub Jan Kvašňák
|
/* External links */
|
|
2023-11-24 16:28
|
Clubfoot (congenital talipes equinovarus)
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 21:12
|
Aplasia radii congenita
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 21:12
|
Miller-Dieker syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 21:09
|
Examination methods in DMP
|
Jakub Jan Kvašňák
|
/* Indications leading to suspicion of DMP */
|
|
2023-11-22 21:09
|
Duchenn's muscular atrophy
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-22 21:01
|
Congenital defects of the inner ear
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 21:00
|
Congenital adrenal hyperplasia
|
Jakub Jan Kvašňák
|
/* Reference */
|
|
2023-11-22 21:00
|
Congenital adrenal hyperplasia
|
Jakub Jan Kvašňák
|
/* Adrenogenital androgenic syndrome */
|
|
2023-11-22 21:00
|
Congenital adrenal hyperplasia
|
Jakub Jan Kvašňák
|
/* 21-hydroxylase deficiency */
|
|
2023-11-22 21:00
|
Congenital adrenal hyperplasia
|
Jakub Jan Kvašňák
|
/* 21-hydroxylase deficiency */
|
|
2023-11-22 20:59
|
Congenital adrenal hyperplasia
|
Jakub Jan Kvašňák
|
/* Adrenal disorders in children */
|
|
2023-11-22 20:57
|
Bartter syndrome
|
Jakub Jan Kvašňák
|
/* Clinical picture */
|
|
2023-11-22 20:57
|
Bartter syndrome
|
Jakub Jan Kvašňák
|
/* Clinical picture */
|
|
2023-11-22 20:56
|
Bartter syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 20:56
|
Bartter syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 20:55
|
Bartter syndrome
|
Jakub Jan Kvašňák
|
/* Pathogenesis */
|
|
2023-11-22 20:41
|
Marfan syndrome
|
Jakub Jan Kvašňák
|
/* Related articles */
|
|
2023-11-22 20:37
|
Hereditary disorders of sugar metabolism
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 20:34
|
Torticollis muscularis congenita
|
Jakub Jan Kvašňák
|
|
|
2023-11-22 20:34
|
Prevention and early diagnosis of birth defects
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 20:33
|
Prevention and early diagnosis of birth defects
|
Jakub Jan Kvašňák
|
|
|
2023-11-22 20:21
|
Amniocentesis
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-22 20:21
|
Fragile X syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-22 20:17
|
Fabry Disease
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-22 20:07
|
Marfan syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-19 20:47
|
Dog equinovarus congenitus
|
Jakub Jan Kvašňák
|
/* External links */
|
|
2023-11-19 11:18
|
Congenita muscularis torticollis
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-19 11:16
|
Primary immunodeficiency
|
Jakub Jan Kvašňák
|
/* Immunodeficiency caused by phagocytosis disorders */
|
|
2023-11-19 11:16
|
Primary immunodeficiency
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-19 11:15
|
Primary immunodeficiency
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-19 11:14
|
Primary ciliary dyskinesia
|
Jakub Jan Kvašňák
|
/* Links */
|
|
2023-11-19 11:07
|
Primary immunodeficiencies
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-17 18:26
|
A palindrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-17 10:51
|
X chromosome
|
Jakub Jan Kvašňák
|
|
|
2023-11-15 19:34
|
Biology and genetics of viruses, importance in medicine
|
Gwenhwyfar Ania Gonnot
|
added links
|
|
2023-11-13 19:55
|
Thanatophoric dwarfism
|
Jakub Jan Kvašňák
|
/* Refrences */
|
|
2023-11-13 19:51
|
Positional defects of the leg
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-13 19:48
|
Severe congenital Kostmann neutropenia
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-12 21:43
|
Promoter
|
Jakub Jan Kvašňák
|
|
|
2023-11-12 21:37
|
Benign
|
Jakub Jan Kvašňák
|
|
|
2023-11-12 09:28
|
Fragile X syndrome
|
Sarah Muller
|
|
|
2023-11-12 09:27
|
Fragile X syndrome
|
Sarah Muller
|
|
|
2023-11-11 23:23
|
Prenatal diagnosis
|
Jakub Jan Kvašňák
|
/* External links */
|
|
2023-11-11 17:27
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:21
|
Dysostosis cleidocranialis
|
Laura Tašková
|
deleted infobox, didnt work properly
|
|
2023-11-11 17:20
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:19
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:17
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:17
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:16
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:16
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:14
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:14
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:13
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:11
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:10
|
Dysostosis cleidocranialis
|
Laura Tašková
|
added infobox
|
|
2023-11-11 17:05
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:04
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 17:02
|
Dysostosis cleidocranialis
|
Laura Tašková
|
|
|
2023-11-11 16:53
|
Dysostosis cleidocranialis
|
Laura Tašková
|
links to correct articles
|
|
2023-11-10 18:55
|
Charcot-Marie-Tooth Syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 18:46
|
Ectodermal dysplasia
|
Jakub Jan Kvašňák
|
/* Used literature */
|
|
2023-11-10 18:36
|
Williams-Beuren syndrome
|
Jakub Jan Kvašňák
|
/* Sources */
|
|
2023-11-10 18:30
|
Enchondromatosis
|
Jakub Jan Kvašňák
|
/* Related articles */
|
|
2023-11-10 18:30
|
Enchondromatosis
|
Jakub Jan Kvašňák
|
/* Related articles */
|
|
2023-11-10 18:21
|
Cherry stain
|
Jakub Jan Kvašňák
|
/* Related articles */
|
|
2023-11-10 11:37
|
Principles of therapy of hereditary diseases
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-10 11:30
|
Crigler-Najjar syndrome
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-10 11:30
|
Zellweger syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:29
|
Wilson's disease
|
Jakub Jan Kvašňák
|
|
|
2023-11-10 11:29
|
Wilson's disease
|
Jakub Jan Kvašňák
|
/* Použitá literatura */
|
|
2023-11-10 11:28
|
Wilson's disease
|
Jakub Jan Kvašňák
|
/* Doporučená literatura */
|
|
2023-11-10 11:13
|
Severe Combined Immunodeficiency Disease
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:11
|
Position dog varus
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:11
|
Position dog varus
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:11
|
Position dog varus
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:11
|
Poland's anomaly
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:10
|
Urea cycle disorders
|
Jakub Jan Kvašňák
|
|
|
2023-11-10 11:08
|
Urea cycle disorders
|
Jakub Jan Kvašňák
|
/* Prognosis */
|
|
2023-11-10 11:07
|
Duane Retraction Syndrome
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-10 11:01
|
DeLange syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-10 11:00
|
Congenital malformations of the auricle
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-09 22:12
|
Rett syndrome
|
Jakub Jan Kvašňák
|
|
|
2023-11-09 22:11
|
Rett syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-09 22:08
|
Fetus
|
Jakub Jan Kvašňák
|
/* Related articles */
|
|
2023-11-09 22:07
|
Fetus
|
Jakub Jan Kvašňák
|
/* Links */
|
|
2023-11-09 21:55
|
Urea Cycle Disorders
|
Jakub Jan Kvašňák
|
/* Reference */
|
|
2023-11-09 21:50
|
Wolf-Hirschhorn syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-08 20:40
|
Leukodystrophy
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-11-08 20:36
|
Metatarsus varus
|
Jakub Jan Kvašňák
|
/* Related articles */
|
|
2023-11-08 20:35
|
Hemoglobinopathies
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-11-08 20:26
|
Hemochromatosis
|
Jakub Jan Kvašňák
|
|
|
2023-11-01 20:52
|
Cystic fibrosis
|
Jakub Jan Kvašňák
|
/* External */
|
|
2023-11-01 20:27
|
Zellweger syndrome
|
Jakub Jan Kvašňák
|
/* References */
|
|
2023-10-29 20:35
|
47, XXX syndrome
|
Jakub Jan Kvašňák
|
|
|
2023-10-29 20:35
|
47, XXX syndrome
|
Jakub Jan Kvašňák
|
|
|
2023-10-29 20:35
|
47, XXX syndrome
|
Jakub Jan Kvašňák
|
|
|
2023-10-02 19:56
|
Alport's syndrome
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 19:48
|
Von Willebrand disease
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 18:28
|
Hemoglobinopathies
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 18:26
|
Hemochromatosis
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 18:24
|
Sickle Cell Anemia
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 18:09
|
Hemoglobinopathies
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 18:08
|
Hemoglobinopathies
|
Ahmed Bahaa Chaban
|
|
|
2023-10-02 18:07
|
Sickle Cell Anemia
|
Ahmed Bahaa Chaban
|
|
|
2023-07-12 09:04
|
Severe congenital Kostmann neutropenia
|
Andrea Rashovska
|
references and categories corrected
|
|
2023-07-12 08:45
|
Congenita muscularis torticollis
|
Andrea Rashovska
|
References and categories corrected
|
|
2023-06-14 16:03
|
Hemochromatosis
|
Egon Lenner
|
|
|
2023-06-14 15:58
|
Hemoglobinopathies
|
Egon Lenner
|
|
|
2023-06-06 20:44
|
Metabolic osteopathy
|
Hakam
|
added citation
|
|
2023-06-02 15:05
|
Pes calcaneovalgus
|
Michael Hartig
|
Hartigm moved page [[Dog calcaneovalgus]] to [[Pes calcaneovalgus]] over redirect
|
me
|
2023-06-02 15:04
|
Pes calcaneovalgus
|
Michael Hartig
|
Undo revision 86785 by [[Special:Contributions/Roshneekesh|Roshneekesh]] ([[User talk:Roshneekesh|talk]])
|
|
2023-06-01 03:09
|
Nuclear envelope
|
Kimia Soltani
|
fixed refrences
|
|
2023-05-31 15:47
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 15:47
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 15:46
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 15:45
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 15:41
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 15:10
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 15:05
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:56
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:40
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:38
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:35
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:34
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:31
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:25
|
Colorectal cancer
|
Tereza Prokšíková
|
|
me
|
2023-05-31 14:23
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:18
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:16
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:14
|
Colorectal cancer
|
Tereza Prokšíková
|
|
me
|
2023-05-31 14:13
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:03
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 14:01
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 13:33
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 13:28
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 13:24
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 13:14
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 12:47
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-31 12:44
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-30 17:27
|
Nuclear envelope
|
Kimia Soltani
|
fixed links,fixed refrences, fixed sentences
|
|
2023-05-30 16:03
|
Pes calcaneovalgus
|
Roshnee Kesh
|
Original text was from WikiSkripta (https://www.wikiskripta.eu/w/Pes_calcaneovalgus)
|
|
2023-05-30 16:01
|
Pes calcaneovalgus
|
Roshnee Kesh
|
Roshneekesh moved page [[Pes calcaneovalgus]] to [[Dog calcaneovalgus]]: Name change
|
me
|
2023-05-30 13:04
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-05-28 22:11
|
Turner's Syndrome
|
Warisha Amir
|
/* MKN-10 classification */
|
|
2023-05-28 22:10
|
Turner's Syndrome
|
Warisha Amir
|
Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
|
|
2023-05-28 22:10
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 22:06
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 22:04
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 22:03
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 22:02
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 22:01
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 21:58
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 21:57
|
Turner's Syndrome
|
Warisha Amir
|
|
|
2023-05-28 21:55
|
Turner's Syndrome
|
Warisha Amir
|
Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
|
|
2023-05-28 21:44
|
Turner's Syndrome
|
Warisha Amir
|
Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
|
|
2023-05-28 21:41
|
Turner's Syndrome
|
Warisha Amir
|
Original test is from: https://www.wikiskripta.eu/w/Turner%C5%AFv_syndrom
|
|
2023-05-24 19:01
|
Screening of congenital developmental defects
|
Matyáš Vláčil
|
Checked by editor
|
|
2023-05-23 15:42
|
Mutation
|
Sofia Filonova
|
References and citation corrected, images corrected
|
|
2023-05-21 09:55
|
Niemann-Pick disease
|
Sofia Filonova
|
Text formatting
|
|
2023-05-21 09:41
|
Niemann-Pick disease
|
Sofia Filonova
|
Categories added, citations and the image corrected
|
|
2023-05-17 19:05
|
Niemann-Pick disease
|
shaan ikrami
|
|
|
2023-05-15 19:07
|
Gene expression
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 19:07
|
Gene expression
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 19:04
|
Gardner's syndrome
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 18:53
|
Duplication
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 18:37
|
Clastogens
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 18:37
|
Congenital strain
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 18:29
|
Genomic DNA
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 18:08
|
Eugenics
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 18:07
|
The gene pool
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 17:55
|
Intercross
|
Jakub Jan Kvašňák
|
|
|
2023-05-15 17:53
|
Fechtner-Epstein syndrome
|
Jakub Jan Kvašňák
|
|
|
2023-05-13 17:34
|
Hyperimmunoglobulinemia IgM syndrome/other types
|
emad alsaeedi
|
|
|
2023-05-13 17:32
|
Hyperimmunoglobulinemia IgM syndrome/other types
|
emad alsaeedi
|
|
|
2023-05-13 17:11
|
Hyperimmunoglobulinemia IgM syndrome/other types
|
emad alsaeedi
|
|
|
2023-05-10 08:14
|
Genetics of intelligence
|
Jakub Jan Kvašňák
|
|
|
2023-05-10 08:14
|
Genetics of intelligence
|
Jakub Jan Kvašňák
|
|
|
2023-05-01 08:54
|
Leukodystrophy
|
Anna Fähnrichová
|
|
me
|
2023-04-30 09:51
|
Apoptosis signaling disorders in tumor cells
|
Sofia Filonova
|
Internal links added, text formatting
|
|
2023-04-29 18:37
|
Hyperimmunoglobulinemia IgM syndrome/other types
|
emad alsaeedi
|
original text from Wikiskripta: Syndrom hyperimunoglobulinemie IgM/další typyhttps://www.wikiskripta.eu/index.php?curid=4130
|
|
2023-04-28 18:15
|
Apoptosis signaling disorders in tumor cells
|
Sofia Filonova
|
Citation corrected, categories added
|
|
2023-04-28 15:39
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-04-28 15:37
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-04-28 15:34
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-04-28 15:31
|
Colorectal cancer
|
Tereza Prokšíková
|
|
|
2023-04-27 20:27
|
Severe congenital Kostmann neutropenia
|
Tali
|
|
|
2023-04-27 20:21
|
Severe congenital Kostmann neutropenia
|
Tali
|
Tali Zerckes- article in translation process
|
|
2023-04-27 19:52
|
Congenita muscularis torticollis
|
Tali
|
|
|
2023-04-27 19:34
|
Congenita muscularis torticollis
|
Tali
|
Tali Zerckes- article in translation process
|
|
2023-04-21 18:42
|
Apoptosis
|
Matyáš Vláčil
|
|
|
2023-04-19 11:22
|
Apoptosis
|
Andrea Rashovska
|
Andyra moved page [[Apoptosis repetition]] to [[Apoptosis]]: corrrection
|
me
|
2023-04-18 17:39
|
Apoptosis and Necrosis
|
Matyáš Vláčil
|
Matt moved page [[Apoptosis]] to [[Apoptosis and Necrosis]]: More fitting name
|
me
|
2023-04-18 17:36
|
Apoptosis
|
Matyáš Vláčil
|
Checked by editor
|
|
2023-04-18 16:41
|
APC resistance
|
Matyáš Vláčil
|
Checked by editor
|
|
2023-04-17 20:04
|
Syndromes due to aneuploidy of autosomes
|
Sofia Filonova
|
Image added, minor visual edits, category corrected
|
|
2023-04-17 17:41
|
Syndromes due to aneuploidy of gonosomes
|
Tereza Bergendyová
|
|
|
2023-04-17 17:41
|
Syndromes due to aneuploidy of gonosomes
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-04-17 17:34
|
Syndromes due to aneuploidy of autosomes
|
Tereza Bergendyová
|
|
|
2023-04-17 17:32
|
Syndromes due to aneuploidy of autosomes
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-04-17 17:31
|
Syndromes due to aneuploidy of autosomes
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-04-17 17:14
|
Syndrome 47, XXY
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-04-17 17:09
|
Syndrome 47,XXX
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-04-15 21:49
|
Fragile X syndrome
|
|
|
|
2023-04-15 21:49
|
Fragile X syndrome
|
|
|
|
2023-04-15 21:47
|
Fragile X syndrome
|
Advay Arora
|
|
|
2023-04-15 21:45
|
Fragile X syndrome
|
Advay Arora
|
Created page with "<!---------------------------------------------------------------------------------------------------------------- * VLOŽENÝ ČLÁNEK * Pozor – tento článek je využí..."
|
|
2023-04-15 09:03
|
Apert syndrome
|
Sofia Filonova
|
Category is corrected, small editions in citation template, small visual editions (image size, notoc)
|
me
|
2023-04-14 17:57
|
Srostlice (obstetrics)
|
Veronika Kousalová
|
|
|
2023-04-14 17:56
|
Srostlice (obstetrics)
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=25248)
|
|
2023-04-14 17:45
|
Syndrome 47, XXY
|
|
Created page with "[[File:I.png|thumb|Karyotype of 47,XYY syndrome]] '''The 47,XYY syndrome''' is caused by the presence of two or more [[wikiskripta:Chromozom_Y|Y chromosomes]] in the karyo..."
|
|
2023-04-14 17:36
|
Syndrome 47,XXX
|
|
everything
|
|
2023-04-14 14:45
|
Collection of chorionic villi
|
RRV8
|
|
|
2023-04-14 14:44
|
Collection of chorionic villi
|
RRV8
|
|
|
2023-04-14 14:39
|
Collection of chorionic villi
|
RRV8
|
|
|
2023-04-14 14:35
|
Collection of chorionic villi
|
RRV8
|
|
|
2023-04-14 14:31
|
Collection of chorionic villi
|
RRV8
|
Created page with "<noinclude>{{Checked | 20190307111556 | [[File:Antonín Šípek.jpg | 30px | link=User:Azrael]] [[User:Azrael|MUDr. Antonín Šípek]] -- WikiSkript:Organization|editing Wik..."
|
|
2023-04-13 19:25
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 19:25
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 19:21
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 19:17
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 18:26
|
Syndromes due to aneuploidy of gonosomes
|
Michalis Papakyriacou
|
Created page with " '''Aneuploidy''' = loss (monosomy) or presence of 1 or more [[chromosomes]] in the [[genome]] of a cell. * Causes: division disorder ( '''nondisjunction''' ) of homologous..."
|
|
2023-04-13 16:39
|
Syndromes due to aneuploidy of autosomes
|
|
Created page with " Aneuploidy refers to the loss (monosomy) or presence of (one or more) chromosomes in the [[genome]] of a cell. '''The cause''' may be a division disorder (nondisjunction) of..."
|
|
2023-04-13 11:20
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 10:54
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 10:44
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 10:04
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 10:02
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 09:58
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-13 09:36
|
Screening of congenital developmental defects
|
Eliška Radová
|
Original text from WikiSkripta: Screening vrozených vývojových vad: https://www.wikiskripta.eu/index.php?curid=3341
|
|
2023-04-11 14:38
|
Chromosomal instability syndromes
|
Michael Hartig
|
Checked by editor
|
|
2023-04-11 14:36
|
Chromosomal instability syndromes
|
Michael Hartig
|
/* Recommended literature */
|
|
2023-04-11 14:36
|
Chromosomal instability syndromes
|
Michael Hartig
|
|
|
2023-04-11 14:36
|
Chromosomal instability syndromes
|
Michael Hartig
|
|
me
|
2023-04-11 06:33
|
Leukodystrophy
|
Erdi Beqiri
|
Original text is from WikiSkripta: https://www.wikiskripta.eu/index.php?curid=22174
|
|
2023-04-11 06:32
|
Leukodystrophy
|
Erdi Beqiri
|
|
|
2023-04-11 06:31
|
Leukodystrophy
|
|
Fixed the links
|
|
2023-04-10 08:04
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-10 07:55
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-09 18:54
|
Congenital disorders of glycosylation
|
Matyáš Vláčil
|
Checked by editor.
|
|
2023-04-09 07:02
|
Wilms' tumor
|
Sofia Filonova
|
|
me
|
2023-04-09 06:58
|
Wilms' tumor
|
Sofia Filonova
|
internal links and category added
|
|
2023-04-09 06:53
|
Wilms' tumor
|
Sofia Filonova
|
citation and references corrected
|
|
2023-04-08 08:42
|
Screening of congenital developmental defects
|
Eliška Radová
|
|
|
2023-04-08 08:38
|
Screening of congenital developmental defects
|
Eliška Radová
|
Original text from WikiSkripta: Screening vrozených vývojových vad: https://www.wikiskripta.eu/index.php?curid=3341
|
|
2023-04-08 08:08
|
Screening of congenital developmental defects
|
Eliška Radová
|
Blanked the page
|
|
2023-04-08 07:48
|
Screening of congenital developmental defects
|
Eliška Radová
|
Original text is from WikiSkripta: Screening vrozených vývojových vad: https://www.wikiskripta.eu/index.php?curid=3341
|
|
2023-04-04 18:32
|
Gonosomal recessive inheritance
|
Sofia Filonova
|
checked by editor
|
|
2023-04-02 18:50
|
Gonosomal recessive inheritance
|
Jowel Jbara
|
|
|
2023-04-02 11:53
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-04-02 07:30
|
Gonosomal dominant inheritance
|
Sofia Filonova
|
checked by editor
|
me
|
2023-04-01 19:26
|
Ehlers–Danlos syndrome
|
Veronika Kousalová
|
|
|
2023-04-01 17:39
|
Gonosomal dominant inheritance
|
Jowel Jbara
|
|
|
2023-04-01 17:39
|
Gonosomal dominant inheritance
|
Jowel Jbara
|
|
|
2023-04-01 12:23
|
Chronic Granulomatous Disease
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-03-31 17:01
|
Metabolic osteopathy
|
Hakam
|
|
|
2023-03-31 17:00
|
Metabolic osteopathy
|
Hakam
|
Original Text from WikiScripta (https://www.wikiskripta.eu/index.php?curid=31312)
|
|
2023-03-31 15:27
|
Chronic Granulomatous Disease
|
Ahmed Bahaa Chaban
|
|
|
2023-03-31 15:26
|
Chronic Granulomatous Disease
|
Ahmed Bahaa Chaban
|
|
|
2023-03-31 15:22
|
Chronic Granulomatous Disease
|
Ahmed Bahaa Chaban
|
|
|
2023-03-31 15:17
|
Chronic Granulomatous Disease
|
Ahmed Bahaa Chaban
|
|
|
2023-03-31 14:27
|
Hemoglobinopathies
|
Tereza Bergendyová
|
|
|
2023-03-31 14:25
|
Hemophilia
|
Tereza Bergendyová
|
|
|
2023-03-31 13:53
|
Hemoglobinopathies
|
Tereza Bergendyová
|
|
|
2023-03-31 13:52
|
Hemoglobinopathies
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-03-31 13:45
|
Hemophilia
|
Tereza Bergendyová
|
|
|
2023-03-31 13:45
|
Hemophilia
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-03-30 13:52
|
Fabry Disease
|
Tereza Bergendyová
|
|
me
|
2023-03-30 13:50
|
Fabry Disease
|
Tereza Bergendyová
|
checked by the editor
|
|
2023-03-29 13:05
|
Hemoglobinopathies
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-03-29 13:04
|
Hemoglobinopathies
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-03-29 13:04
|
Hemoglobinopathies
|
Jakub Jan Kvašňák
|
/* Source */
|
|
2023-03-29 13:03
|
Hemoglobinopathies
|
Jakub Jan Kvašňák
|
|
|
2023-03-28 18:56
|
Hemoglobinopathies
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 18:51
|
Hemoglobinopathies
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 18:50
|
Hemoglobinopathies
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 18:43
|
Hemoglobinopathies
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 18:35
|
Hemophilia
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 18:34
|
Hemophilia
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 18:34
|
Hemophilia
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 15:18
|
Hemophilia
|
Kiana Sadehmeymandi
|
|
|
2023-03-28 15:13
|
Hemophilia
|
Jakub Jan Kvašňák
|
|
|
2023-03-28 15:11
|
Hemophilia
|
Jakub Jan Kvašňák
|
|
|
2023-03-28 15:11
|
Hemophilia
|
Jakub Jan Kvašňák
|
|
|
2023-03-28 15:11
|
Hemophilia
|
Jakub Jan Kvašňák
|
|
|
2023-03-28 13:26
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:46
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:44
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:43
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:43
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:42
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|
2023-03-27 21:41
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:39
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:39
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|
2023-03-27 21:36
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:34
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|
2023-03-27 21:34
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:33
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:31
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:30
|
Fabry Disease
|
Veronika Kousalová
|
|
|
2023-03-27 21:23
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|
2023-03-27 21:22
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|
2023-03-27 21:18
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|
2023-03-27 21:09
|
Fabry Disease
|
Veronika Kousalová
|
Original text from (https://www.wikiskripta.eu/index.php?curid=69060)
|
|