Down syndrome congenital heart disease: A narrowed region and a candidate gene

Genetics in Medicine

Volumn 3, Issue 2, 2001, Pages 91-101

  Barlow, Gillian M ^a   Chen, Xiao Ning ^a   Shi, Zheng Y ^a   Lyons, Gary E ^a   Kurnit, David M ^a   Celle, Livija ^a   Spinner, Nancy B ^a   Zackai, Elaine ^a   Pettenati, Mark J ^a   Van Riper, Alexander J ^a   Vekemans, Michael J ^a   Mjaatvedt, Corey H ^a   Korenberg, Julie R ^a  

^a CEDARS SINAI MEDICAL CENTER   (United States)

Author keywords

Chromosome 21; Congenital heart disease; Down syndrome; Genes in development; Morphogenesis

Indexed keywords

CELL ADHESION MOLECULE; COLLAGEN; COLLAGEN TYPE 18; COLLAGEN TYPE 6; COLLAGEN TYPE 6 A1; COLLAGEN TYPE 6 A2; DOWN SYNDROME CELL ADHESION MOLECULE; MOLECULAR MARKER; UNCLASSIFIED DRUG;

ARTICLE; CHROMOSOMAL LOCALIZATION; CHROMOSOME 21; CHROMOSOME 21Q; CHROMOSOME 21Q11.2; CHROMOSOME DUPLICATION; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; DOWN SYNDROME; FALLOT TETRALOGY; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE EXPRESSION; GENETIC ANALYSIS; HEART ATRIUM SEPTUM DEFECT; HEART DEVELOPMENT; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; MALE; MOLECULAR DYNAMICS; MORPHOGENESIS; PARTIAL TRISOMY; QUANTITATIVE ANALYSIS; SOUTHERN BLOTTING; TELOMERE; TRISOMY 21;

EID: 18544383778     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/00125817-200103000-00002     Document Type: Article

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