Wawrocka, Anna <br/><br/>
11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia.  [electronic resource] 

 -  Journal of applied genetics  Aug 2013 
 - 345-51 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2190-3883 
<br/><br/><label>Standard No.: </label>10.1007/s13353-013-0154-0  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aniridia--ethnology<br/>Base Sequence<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 11<br/>DNA Primers--genetics<br/>Exons<br/>Eye Proteins--genetics<br/>Gene Deletion<br/>Genomics<br/>Heterozygote<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Introns<br/>Molecular Sequence Data<br/>Mutation<br/>PAX6 Transcription Factor<br/>Paired Box Transcription Factors--genetics<br/>Phenotype<br/>Point Mutation<br/>Poland<br/>Repressor Proteins--genetics