Goldmuntz, E <br/><br/>
Frequency of 22q11 deletions in patients with conotruncal defects.  [electronic resource] 

 -  Journal of the American College of Cardiology  Aug 1998 
 - 492-8 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0735-1097 
<br/><br/><label>Standard No.: </label>10.1016/s0735-1097(98)00259-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aorta, Thoracic--abnormalities<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22--genetics<br/>DiGeorge Syndrome--genetics<br/>Double Outlet Right Ventricle--genetics<br/>Face--abnormalities<br/>Female<br/>Genetic Testing<br/>Heart Defects, Congenital--genetics<br/>Heart Septal Defects, Ventricular--genetics<br/>Humans<br/>Incidence<br/>Male<br/>Prospective Studies<br/>Pulmonary Artery--abnormalities<br/>Syndrome<br/>Tetralogy of Fallot--genetics<br/>Transposition of Great Vessels--genetics<br/>Truncus Arteriosus, Persistent--genetics