Chromosome abnormalities in congenital heart disease

American Journal of Medical Genetics

Volumn 70, Issue 3, 1997, Pages 292-298

  Johnson, Mark C ^a,b   Hing, Anne ^a   Wood, Mary K ^a   Watson, Michael S ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

22q deletion; 8p deletion; Conotruncal congenital heart defects

Indexed keywords

ARTICLE; CHROMOSOME 22Q; CHROMOSOME 7Q; CHROMOSOME 8P; CHROMOSOME ABERRATION; CONGENITAL HEART DISEASE; CYTOGENETICS; FALLOT TETRALOGY; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; MAJOR CLINICAL STUDY; MALE; PREVALENCE; PRIORITY JOURNAL;

CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; HEART DEFECTS, CONGENITAL; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; PREVALENCE;

EID: 0031005732     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970613)70:3<292::AID-AJMG15>3.0.CO;2-G     Document Type: Article

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