McDonald-McGinn, Donna M <br/><br/>
Craniosynostosis: another feature of the 22q11.2 deletion syndrome.  [electronic resource] 

 -  American journal of medical genetics. Part A  Aug 2005 
 - 358-62 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1552-4825 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.30746  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>Craniosynostoses--genetics<br/>Fatal Outcome<br/>Female<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Syndrome