Coman, David J <br/><br/>
Two siblings with 46,XY DSD, congenital adrenal hypoplasia, aniridia, craniofacial, and skeletal abnormalities and intrauterine growth retardation: a new syndrome?  [electronic resource] 

 -  American journal of medical genetics. Part A  Sep 2007 
 - 2085-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.31894  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adrenal Insufficiency--congenital<br/>Aniridia--genetics<br/>Bone and Bones--abnormalities<br/>Face--abnormalities<br/>Fetal Growth Retardation--genetics<br/>Humans<br/>Infant, Newborn<br/>Karyotyping<br/>Male<br/>Skull--abnormalities<br/>Syndrome