High Incidence of GJB2 Mutations During Screening of Newborns for Hearing Loss in Austria-Reference-Cited by-同舟云学术

High Incidence of GJB2 Mutations During Screening of Newborns for Hearing Loss in Austria

Published:2007-06 Issue:3 Volume:28 Page:298-301
ISSN:0196-0202
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Ramsebner Reinhard,Volker Romana,Lucas Trevor,Hamader Gertrude,Weipoltshammer Klara,Baumgartner Wolf-Dieter,Wachtler Franz J.,Kirschhofer Karin,Frei Klemens

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference24 articles.

1. Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafness.;Bathelier;Genetic Counseling,2004

2. Epidemiology, etiology and genetic patterns (pp. 9–21).;Cohen,1995

3. Connexin-26 mutations in sporadic and inherited sensorineural deafness.;Estivill;Lancet,1998

4. Lack of association between Connexin 31 (GJB3) alterations and sensorineural deafness in Austria.;Frei;Hearing Research,2004a

5. Screening for monogenetic del(GJB6-D13S1830) and digenic del(GJB6-D13S1830)/GJB2 patterns of inheritance in deaf individuals from Eastern Austria.;Frei;Hearing Research,2004b

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