Marino, B <br/><br/>
Anatomic patterns of conotruncal defects associated with deletion 22q11.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics   
 - 45-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-3600 
<br/><br/><label>Standard No.: </label>10.1097/00125817-200101000-00010  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Aorta, Thoracic--abnormalities<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22<br/>DiGeorge Syndrome--diagnosis<br/>Female<br/>Genotype<br/>Heart Defects, Congenital--diagnosis<br/>Heart Septal Defects, Ventricular--diagnosis<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Phenotype<br/>Pulmonary Atresia--diagnosis<br/>Tetralogy of Fallot--diagnosis<br/>Truncus Arteriosus--abnormalities