van Bever, Yolande <br/><br/>
Exclusion of a PAX6, FOXC1, PITX2, and MYCN mutation in another patient with apple peel intestinal atresia, ocular anomalies and microcephaly and review of the literature.  [electronic resource] 

 -  American journal of medical genetics. Part A  Feb 2008 
 - 500-4 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.32169  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>DNA Mutational Analysis<br/>Eye Abnormalities--complications<br/>Eye Proteins--genetics<br/>Female<br/>Forkhead Transcription Factors--genetics<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Infant<br/>Intestinal Atresia--complications<br/>Microcephaly--complications<br/>Mutation<br/>N-Myc Proto-Oncogene Protein<br/>Nuclear Proteins--genetics<br/>Oncogene Proteins--genetics<br/>PAX6 Transcription Factor<br/>Paired Box Transcription Factors--genetics<br/>Repressor Proteins--genetics<br/>Transcription Factors--genetics<br/>Homeobox Protein PITX2