Bidinost, Carla <br/><br/>
Heterozygous and homozygous mutations in PITX3 in a large Lebanese family with posterior polar cataracts and neurodevelopmental abnormalities.  [electronic resource] 

 -  Investigative ophthalmology & visual science  Apr 2006 
 - 1274-80 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0146-0404 
<br/><br/><label>Standard No.: </label>10.1167/iovs.05-1095  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cataract--genetics<br/>Chromosomes, Human, Pair 10--genetics<br/>Consanguinity<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Linkage<br/>Haplotypes<br/>Heterozygote<br/>Homeodomain Proteins--genetics<br/>Homozygote<br/>Humans<br/>Lebanon<br/>Lod Score<br/>Male<br/>Microphthalmos--genetics<br/>Mutation<br/>Nervous System Diseases--genetics<br/>Pedigree<br/>Transcription Factors--genetics