Hearing impairment caused by mutations in two different genes responsible for nonsyndromic and syndromic hearing loss within a single family

• Autorzy: Niepokoj K. , Rygiel A.M. , Jurczak P. , Kujko A.A. , Sniegorska D. , Sawicka J. , Grabarczyk A. , Bal J. , Wertheim-Tysarowska K.
• Języki publikacji: EN

Abstrakty

EN

• Wydawca: -
• Czasopismo: Journal of Applied Genetics
• Rocznik: 2018
• Tom: 59
• Numer: 1
• Opis fizyczny: p.67-72,fig.,ref.

Twórcy

autor

Niepokoj K.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

Rygiel A.M.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

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

autor

Kujko A.A.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

Sniegorska D.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

Sawicka J.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

Grabarczyk A.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

Bal J.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

autor

Wertheim-Tysarowska K.

• Department of Medical Genetics, Institute of Mother and Child, Kasprzaka 17a, 01-211, Warsaw, Poland

Identyfikatory

DOI

10.1007/s13353-017-0416-3