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PEER REVIEWED PUBLICATIONS;
1. DFNB89, a novel autosomal recessive nonsyndromic hearing impairment locus on chromosome 16q21-q23.2.
Hum Genet. 2010 Dec 22,,
2. A novel splice-acceptor site mutation in CDH3 gene in a consanguineous family exhibiting hypotrichosis with juvenile macular dystrophy. Arch Dermatol Res. 2010 Nov;302(9):701-3. Mapping of a novel autosomal recessive hypotrichosis locus on chromosome 10q11.23-22.3.. 2010 Jan 7.
4. Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia. Epub 2009 Jun 24.
5- Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis ...
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