Fares-Taie, Lucas <br/><br/>
Submicroscopic deletions at 13q32.1 cause congenital microcoria.  [electronic resource] 

 -  American journal of human genetics  Apr 2015 
 - 631-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2015.01.014  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 13--genetics<br/>Comparative Genomic Hybridization<br/>Gene Components<br/>Genes, Dominant--genetics<br/>Humans<br/>Hydro-Lyases--genetics<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Oligonucleotide Array Sequence Analysis<br/>Pedigree<br/>Pupil Disorders--congenital<br/>Receptors, Cell Surface--genetics<br/>Receptors, G-Protein-Coupled<br/>Sequence Analysis, DNA