Effect of copy number variants on outcomes for infants with single ventricle heart defects

Circulation: Cardiovascular Genetics

Volumn 6, Issue 5, 2013, Pages 444-451

  Carey, Abigail S ^a   Liang, Li ^a   Edwards, Jonathan ^a   Brandt, Tracy ^a   Mei, Hui ^a   Sharp, Andrew J ^a   Hsu, Daphne T ^b   Newburger, Jane W ^c   Ohye, Richard G ^d   Chung, Wendy K ^e   Russell, Mark W ^f   Rosenfeld, Jill A ^g   Shaffer, Lisa G ^h   Parides, Michael K ^a   Edelmann, Lisa ^a   Gelb, Bruce D ^a  

^a MOUNT SINAI SCHOOL OF MEDICINE   (United States)

^b CHILDREN S HOSPITAL AT MONTEFIORE   (United States)

^c BOSTON CHILDREN S HOSPITAL   (United States)

^d UNIVERSITY OF MICHIGAN MEDICAL SCHOOL   (United States)

^e New York Presbyterian Morgan Stanley Children's Hospital   (United States)

^f UNIVERSITY OF MICHIGAN   (United States)

^g PERKINELMER INC   (United States)

^h Genetic Veterinary Sciences   (United States)

Author keywords

Congenital cardiac defect; DNA copy number variantiations; Hypoplastic left heart syndrome; Outcome

Indexed keywords

GENOMIC DNA; TRANSCRIPTION FACTOR GATA 4;

ARTICLE; CHILD GROWTH; CHROMOSOME ABERRATION; COGNITION; COMPARATIVE GENOMIC HYBRIDIZATION; CONGENITAL HEART DISEASE; CONTROLLED STUDY; COPY NUMBER VARIATION; FEMALE; GENE; GENE DELETION; GENE DUPLICATION; GENOTYPE; GJA5 GENE; HEART SINGLE VENTRICLE; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MYH11 GENE; PREVALENCE; PRIORITY JOURNAL;

CONGENITAL CARDIAC DEFECT; DNA COPY NUMBER VARIANTIATIONS; HYPOPLASTIC LEFT HEART SYNDROME; OUTCOME;

CASE-CONTROL STUDIES; COHORT STUDIES; COMPARATIVE GENOMIC HYBRIDIZATION; CONNEXINS; DNA COPY NUMBER VARIATIONS; GATA4 TRANSCRIPTION FACTOR; GENOME, HUMAN; GENOTYPE; HEART DEFECTS, CONGENITAL; HUMANS; INFANT; MYOSIN HEAVY CHAINS; PREVALENCE;

EID: 84892379085     PISSN: 1942325X     EISSN: 19423268     Source Type: Journal    
DOI: 10.1161/CIRCGENETICS.113.000189     Document Type: Article

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