Your browser doesn't support javascript.
loading
Identification of a novel pathogenic OTOF variant causative of nonsyndromic hearing loss with high frequency in the Ashkenazi Jewish population.
Fedick, Anastasia M; Jalas, Chaim; Swaroop, Ananya; Smouha, Eric E; Webb, Bryn D.
Afiliación
  • Fedick AM; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Jalas C; Bonei Olam, Center for Rare Jewish Genetic Disorders, Brooklyn, NY, USA.
  • Swaroop A; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Smouha EE; Department of Otolaryngology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Webb BD; Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Appl Clin Genet ; 9: 141-6, 2016.
Article en En | MEDLINE | ID: mdl-27621663
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Appl Clin Genet Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Diagnostic_studies Idioma: En Revista: Appl Clin Genet Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos