VOHWINKEL SYNDROME; VOWNKL

Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary

Literature (1)

Literature for OMIM 124500: VOHWINKEL SYNDROME; VOWNKL

Xenbase Articles:
(

Denotes literature images)

GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf., Tekin M,Xia XJ,Cengiz FB,White TW,Radnaabazar J,Tastan H,Nance WE,Pandya A,Dangaasuren B,Erdenetungalag R, Ann Hum Genet. March 1, 2010; 74(2):1469-1809.

GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf., Tekin M,Xia XJ,Cengiz FB,White TW,Radnaabazar J,Tastan H,Nance WE,Pandya A,Dangaasuren B,Erdenetungalag R, Ann Hum Genet. March 1, 2010; 74(2):1469-1809.