Congenital anal anomalies in two families with the Opitz G syndrome.

Five children from two families presented to a regional neonatal surgical unit between 1959 and 1984 with congenital anal anomalies and other malformations resulting from an autosomal dominant inherited condition, the Opitz G syndrome. This and other Mendelian causes of congenital anal malformations...

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Main Authors: Tolmie, J L, Coutts, N, Drainer, I K
Format: Artigo
Sprog:Inglês
Udgivet: 1987
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050347/
https://ncbi.nlm.nih.gov/pubmed/3430544
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