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Exclusion of RET and Pax 3 loci in Waardenburg-Hirschsprung disease.

The RET and the Pax 3 genes have recently been shown to account for autosomal dominant Hirschsprung's disease (HSCR) and Waardenburg syndrome type 1 (WS1) respectively, which led us to consider them as candidate genes in the WS/HSCR association. Linkage analyses performed in a consanguineous WS...

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Detalhes bibliográficos
Main Authors: Attié, T, Till, M, Pelet, A, Edery, P, Bonnet, J P, Munnich, A, Lyonnet, S
Formato: Artigo
Idioma:Inglês
Publicado em: 1995
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050384/
https://ncbi.nlm.nih.gov/pubmed/7643365
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