Polydactyly
From WikiLectures
Template:Infobox - genetic disease
'Polydactyly is a congenital defect characterized by supernumerary fingers or toes. It is often hereditary. This trait is conditioned by the dominant mutant allele P [1], the effect of which will only be felt by some wearers. Polydactyly therefore belongs to disabilities with incomplete penetrance.
It occurs, for example, with trisomy 13. chromosomeu, which is called Patau syndrome.
Links[edit | edit source]
References[edit | edit source]
„ | {{{1}}} | “ |
- {{#switch: book
|book =
Incomplete publication citation. SNUSTAD, D. Peter. Genetics. Brno : Masaryk University, 2009. 978-80-7262-438-6.
|collection =
Incomplete citation of contribution in proceedings. SNUSTAD, D. Peter. Genetics. Brno : Masaryk University, 2009. {{ #if: 978-80-210-4852-2 |978-80-7262-438-6} } |article = Incomplete article citation. SNUSTAD, D. Peter. 2009, year 2009,
|web =
Incomplete site citation. SNUSTAD, D. Peter. Masaryk University, ©2009.
|cd =
Incomplete carrier citation. SNUSTAD, D. Peter. Masaryk University, ©2009.
|db =
Incomplete database citation. Masaryk University, ©2009.
|corporate_literature =
SNUSTAD, D. Peter. Genetics. Brno : Masaryk University, 2009. 978-80-7262-438-6} }
References[edit | edit source]
- ↑ {{#switch: book |book = Incomplete publication citation. SNUSTAD, D. Peter. Genetics. Brno : Masaryk University, 2009. 871 s. 978-80-7262-438-6. |collection = Incomplete citation of contribution in proceedings. SNUSTAD, D. Peter. Genetics. Brno : Masaryk University, 2009. 871 s. {{ #if: 978-80-210-4852-2 |978-80-7262-438-6} } |article = Incomplete article citation. SNUSTAD, D. Peter. 2009, year 2009, |web = Incomplete site citation. SNUSTAD, D. Peter. Masaryk University, ©2009. |cd = Incomplete carrier citation. SNUSTAD, D. Peter. Masaryk University, ©2009. |db = Incomplete database citation. Masaryk University, ©2009. |corporate_literature = SNUSTAD, D. Peter. Genetics. Brno : Masaryk University, 2009. 871 s. 978-80-7262-438-6} }