Hearing loss in Waardenburg syndrome: a systematic review.

Song, J; Feng, Y; Acke, F R; Coucke, P; Vleminckx, K; Dhooge, I J

Song, J; Feng, Y; Acke, F R; Coucke, P; Vleminckx, K; Dhooge, I J.

Afiliação

Song J; Department of Otolaryngology, Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Feng Y; Department of Otolaryngology, Xiangya Hospital, Central South University, Changsha, People's Republic of China.
Acke FR; Department of Otorhinolaryngology, Ghent University/Ghent University Hospital, Ghent, Belgium.
Coucke P; Department of Medical Genetics, Ghent University/Ghent University Hospital, Ghent, Belgium.
Vleminckx K; Department of Medical Genetics, Ghent University/Ghent University Hospital, Ghent, Belgium.
Dhooge IJ; Department for Biomedical Molecular Biology, Ghent University, Ghent, Belgium.

Clin Genet ; 89(4): 416-425, 2016 Apr.

Article em En | MEDLINE | ID: mdl-26100139

Palavras-chave

Waardenburg syndrome; genotype; hearing loss; inner ear malformation; phenotype

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies / Systematic_reviews Idioma: En Revista: Clin Genet Ano de publicação: 2016 Tipo de documento: Article País de publicação: Dinamarca

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