Basit, S <br/><br/>
Digenic inheritance of an autosomal recessive hypotrichosis in two consanguineous pedigrees.  [electronic resource] 

 -  Clinical genetics  Mar 2011 
 - 273-81 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2010.01455.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 12<br/>Chromosomes, Human, Pair 16<br/>Consanguinity<br/>Female<br/>Genes, Recessive<br/>Genetic Linkage<br/>Genotype<br/>Humans<br/>Hypotrichosis--genetics<br/>Male<br/>Mutation<br/>Pakistan<br/>Pedigree<br/>Phenotype