Atrioventricular septal defect with pulmonary atresia in DiGeorge anomaly: Expansion of the cardiac phenotype

American Journal of Medical Genetics

Volumn 61, Issue 1, 1996, Pages 89-91

  Kumar, A ^a   Sapire, D W ^a   Lockhart, L H ^a   McCombs, J L ^a   Hawkins, H K ^a   Van Mierop, L H S ^a  

^a UNIVERSITY OF TEXAS MEDICAL BRANCH   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CD16 ANTIGEN; CD19 ANTIGEN; CD3 ANTIGEN; CD4 ANTIGEN; CD8 ANTIGEN; PROSTAGLANDIN E;

ANGIOGRAPHY; CASE REPORT; DIGEORGE SYNDROME; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HEART ATRIUM SEPTUM DEFECT; HEART CATHETERIZATION; HUMAN; LETTER; LUNG ATRESIA; NEURAL CREST; NEWBORN; PRIORITY JOURNAL;

ADULT; ANTIGENS, CD; ATRIOVENTRICULAR NODE; CHROMOSOMES, HUMAN, PAIR 22; DIABETES MELLITUS, TYPE 1; DIGEORGE SYNDROME; FEMALE; HEART SEPTAL DEFECTS; HUMANS; INFANT, NEWBORN; PREGNANCY; PREGNANCY IN DIABETICS; PULMONARY ATRESIA; PULMONARY CIRCULATION; T-LYMPHOCYTE SUBSETS;

EID: 0030032775     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.1320610104     Document Type: Letter

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