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Two brothers with the Marden-Walker syndrome: case report and review

Two brothers with blepharophimosis, congenital joint contractures, and mental retardation characteristic of the Marden-Walker syndrome are described. This sib pair strengthens the case for autosomal recessive inheritance of the syndrome.

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Detalhes bibliográficos
Main Authors: Howard, Frances M, Rowlandson, Piers
Formato: Artigo
Idioma:Inglês
Publicado em: 1981
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1048658/
https://ncbi.nlm.nih.gov/pubmed/7252998
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