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Molecular Study of Three Lebanese and Syrian Patients with Waardenburg Syndrome and Report of Novel Mutations in the EDNRB and MITF Genes.
Haddad, N M; Ente, D; Chouery, E; Jalkh, N; Mehawej, C; Khoueir, Z; Pingault, V; Mégarbané, A.
Affiliation
  • Haddad NM; Unité de Génétique Médicale et Laboratoire Associé INSERM UMR-S910, Faculté de Médecine, Université Saint-Joseph, Beirut, Lebanon.
Mol Syndromol ; 1(4): 169-175, 2011 Jan.
Article in En | MEDLINE | ID: mdl-21373256
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Syndromol Year: 2011 Document type: Article
Fulltext
Print
XML
PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mol Syndromol Year: 2011 Document type: Article