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Familial occurrence of omphalocele suggesting sex-linked inheritance.

A family is described in which 4 males in two generations had omphalocele. There was no case of omphalocele in any of the women. It is suggested that the mode of inheritance could be a sex-linked recessive trait.

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Hlavní autoři: Havalad, S, Noblett, H, Speidel, B D
Médium: Artigo
Jazyk:Inglês
Vydáno: 1979
Témata:
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1545351/
https://ncbi.nlm.nih.gov/pubmed/434891
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