Your browser doesn't support javascript.
loading
Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family.
Niepokój, Katarzyna; Rygiel, Agnieszka M; Jurczak, Piotr; Kujko, Aleksandra A; Sniegórska, Dominika; Sawicka, Justyna; Grabarczyk, Alicja; Bal, Jerzy; Wertheim-Tysarowska, Katarzyna.
Afiliación
  • Niepokój K; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland. katarzyna.niepokoj@imid.med.pl.
  • Rygiel AM; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
  • Jurczak P; Center of Diagnosis, Treatment and Rehabilitation of Hearing, Voice and Speech Disorders, John Paul II Podkarpacie Province Hospital, Korczynska Street, 38-400, Krosno, Poland.
  • Kujko AA; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
  • Sniegórska D; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
  • Sawicka J; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
  • Grabarczyk A; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
  • Bal J; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
  • Wertheim-Tysarowska K; Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a Street, 01-211, Warsaw, Poland.
J Appl Genet ; 59(1): 67-72, 2018 Feb.
Article en En | MEDLINE | ID: mdl-29151245
Asunto(s)
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 Asunto principal: Sordera / Síndromes de Usher Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Appl Genet Asunto de la revista: GENETICA Año: 2018 Tipo del documento: Article País de afiliación: Polonia
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Sordera / Síndromes de Usher Límite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: J Appl Genet Asunto de la revista: GENETICA Año: 2018 Tipo del documento: Article País de afiliación: Polonia