Prevalence and nature of connexin 26 mutations in children with non‐syndromic deafness-Reference-Cited by-同舟云学术

Prevalence and nature of connexin 26 mutations in children with non‐syndromic deafness

Published:2001-08 Issue:4 Volume:175 Page:191-194
ISSN:0025-729X
Container-title:Medical Journal of Australia
language:en
Short-container-title:Medical Journal of Australia

Author:

Dahl Hans‐Henrik M¹,Saunders Kerryn²,Kelly Therese M¹,Osborn Amelia H¹,Wilcox Stephen¹,Cone‐Wesson Barbara³,Wunderlich Julia L⁴,Du Sart Desiree¹,Kamarinos Maria¹,Gardner Robert J McKinlay¹,Dennehy Shirley⁵,Williamson Robert¹,Vallance Neil⁶,Mutton Patricia⁷

Affiliation:

1. Murdoch Children's Research Institute, Victorian Clinical Genetics Service, and Department of PaediatricsUniversity of Melbourne, Royal Children's HospitalMelbourneVIC

2. Department of PaediatricsSouthern Health and Monash UniversityMelbourneVIC

3. Department of OtolaryngologyUniversity of MelbourneMelbourneVIC

4. Department of AudiologySouthern HealthMelbourneVIC

5. Taralye137 Blackburn RoadMelbourneVIC

6. Department of ENT and Head and Neck SurgerySouthern HealthMelbourneVIC

7. The Deafness CentreThe Children's Hospital at WestmeadSydneyNSW

Publisher

AMPCo

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.2001.tb143093.x