The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease

Human Genetics

Volumn 133, Issue 1, 2014, Pages 11-27

  Warburton, Dorothy ^a   Ronemus, Michael ^b   Kline, Jennie ^c   Jobanputra, Vaidehi ^a   Williams, Ismee ^a   Anyane Yeboa, Kwame ^a   Chung, Wendy ^a   Yu, Lan ^a   Wong, Nancy ^a   Awad, Danielle ^a   Yu, Chih Yu ^a   Leotta, Anthony ^b   Kendall, Jude ^b   Yamrom, Boris ^b   Lee, Yoon Ha ^b   Wigler, Michael ^b   Levy, Dan ^b  

^a Och Spine at New York Presbyterian Hospitals   (United States)

^b Howard Hughes Medical Institute Cold Spring Harbor Laboratory Cold Spring Harbor   (United States)

^c NEW YORK STATE PSYCHIATRIC INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN NODAL; TRANSCRIPTION FACTOR GATA 4;

ARTICLE; CHILD; CHROMOSOME 22Q; COMPARATIVE GENOMIC HYBRIDIZATION; CONTROLLED STUDY; COPY NUMBER VARIATION; DIGEORGE SYNDROME; FEMALE; GENE DELETION; HEART DEVELOPMENT; HUMAN; HYPOPLASTIC LEFT HEART SYNDROME; MAJOR CLINICAL STUDY; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 84891879501     PISSN: 03406717     EISSN: 14321203     Source Type: Journal    
DOI: 10.1007/s00439-013-1353-9     Document Type: Article

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