Homozygosity for autosomal dominant Marfan syndrome.

Marfan syndrome is an autosomal dominant condition with varying phenotypic manifestations. Affected persons are usually heterozygotes. A family is presented in which the gene for this syndrome is segregating in a large number of members. Two sibs suffered from unusually severe, identical, and fatal...

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Bibliografiske detaljer
Main Authors: Chemke, J, Nisani, R, Feigl, A, Garty, R, Cooper, M, Bårash, Y, Duksin, D
Format: Artigo
Sprog:Inglês
Udgivet: 1984
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1049260/
https://ncbi.nlm.nih.gov/pubmed/6748012
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