Mani, Arya <br/><br/>
Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorder.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Feb 2005 
 - 2975-9 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.0409852102  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adult<br/>Bone and Bones--abnormalities<br/>DNA-Binding Proteins--genetics<br/>Ductus Arteriosus, Patent--genetics<br/>Female<br/>Genetic Linkage<br/>Haplotypes<br/>Humans<br/>Mutation<br/>Sleep Wake Disorders--genetics<br/>Tooth Abnormalities--genetics<br/>Transcription Factor AP-2<br/>Transcription Factors--genetics