Keser, Vafa <br/><br/>
The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families.  [electronic resource] 

 -  Investigative ophthalmology & visual science  02 2017 
 - 1028-1036 p.  digital 
<br/><br/> Publication Type: Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-5783 
<br/><br/><label>Standard No.: </label>10.1167/iovs.16-20281  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Basic Helix-Loop-Helix Transcription Factors--genetics<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>Genotype<br/>Helix-Loop-Helix Motifs<br/>Humans<br/>Incidence<br/>Infant<br/>Male<br/>Mutation<br/>Pakistan--epidemiology<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Retina--metabolism<br/>Retinal Diseases--congenital