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Pitfalls of genetic counselling in Pfeiffer's syndrome.

A family with Pfeiffer's syndrome is presented in which members of two generations showed only partial but relevant syndactyly before a child was born, in the third generation, with the full acrocephalosyndactyly syndrome.

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Detalhes bibliográficos
Main Authors: Baraitser, M, Bowen-Bravery, M, Saldaña-Garcia, P
Formato: Artigo
Idioma:Inglês
Publicado em: 1980
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048564/
https://ncbi.nlm.nih.gov/pubmed/7205899
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