Neural tube defects and deletions of 22q11

American Journal of Medical Genetics

Volumn 66, Issue 1, 1996, Pages 25-27

  Nickel, Robert E ^a,b   Magenis, R Ellen ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b NONE   (United States)

Author keywords

cleft palate; congenital heart defect; conotruncal heart defect; deletion 22q11; DiGeorge sequence; meningomyelocele; neural tube defect; velo cardio facial syndrome

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; DIGEORGE SYNDROME; DISEASE ASSOCIATION; FAMILY HISTORY; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; MAJOR CLINICAL STUDY; NEURAL TUBE DEFECT; PRIORITY JOURNAL;

CHILD; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; GENETIC MARKERS; HEART DEFECTS, CONGENITAL; HUMANS; NEURAL TUBE DEFECTS;

EID: 0029956830     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19961202)66:1<25::AID-AJMG6>3.0.CO;2-V     Document Type: Article

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