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Risk counselling in autosomal dominant disorders with undetermined penetrance.

A method is presented for estimating the probability of an affected child being born to a clinically unaffected subject who is at risk for having inherited a rare gene for an autosomal dominant disorder of unknown penetrance. The maximal risk is 8.6% for children of persons at 50% risk for having in...

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Detalhes bibliográficos
Main Authors: Pauli, R M, Motulsky, A G
Formato: Artigo
Idioma:Inglês
Publicado em: 1981
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048754/
https://ncbi.nlm.nih.gov/pubmed/7328613
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