Driscoll, D A <br/><br/>
Prenatal diagnosis of the 22q11.2 deletion syndrome.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics   
 - 14-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.; Review 
<br/><br/><label>ISSN: </label>1098-3600 
<br/><br/><label>Standard No.: </label>10.1097/00125817-200101000-00004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple<br/>Adult<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22<br/>DiGeorge Syndrome--diagnosis<br/>Facies<br/>Female<br/>Gene Deletion<br/>Genetic Counseling<br/>Humans<br/>In Situ Hybridization, Fluorescence--methods<br/>Male<br/>Phenotype<br/>Polymerase Chain Reaction--methods<br/>Prenatal Diagnosis<br/>Risk Factors<br/>Syndrome