Waardenburg syndrome: A rare genetic disorder, a report of two cases.

Kumar, Sudesh; Rao, Kiran.

Indian J Hum Genet ; 2012 May; 18(2): 254-255

Article in En | IMSEAR | ID: sea-143283

Key words

Autosomal dominant; deafness; heterochromia; pigmentation anomalies; Waardenburg syndrome

Full text: 1 Index: IMSEAR Language: En Journal: Indian J Hum Genet Year: 2012 Type: Article

Full text: 1 Index: IMSEAR Language: En Journal: Indian J Hum Genet Year: 2012 Type: Article