GATA4 haploinsufficiency in patients with interstitial deletion of chromosome region 8p23.1 and congenital heart disease

American Journal of Medical Genetics

Volumn 83, Issue 3, 1999, Pages 201-206

  Pehlivan, Tugce ^a   Pober, Barbara R ^a   Brueckner, Martina ^a   Garrett, Stacey ^b   Slaugh, Rachel ^b   Van Rheeden, Richard ^b   Wilson, David B ^b,c   Watson, Michael S ^b   Hing, Anne V ^b  

^a YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c ST LOUIS CHILDREN S HOSPITAL   (United States)

Author keywords

Chromosome 8p23.1; Congenital heart disease; Heart development; Transcription factor GATA 4

Indexed keywords

TRANSCRIPTION FACTOR; ZINC FINGER PROTEIN;

ADULT; ARTICLE; CHILD; CHROMOSOME 8P; CHROMOSOME DELETION; CLINICAL ARTICLE; CONGENITAL HEART DISEASE; CONGENITAL HEART MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENETIC TRANSCRIPTION; HEART DEVELOPMENT; HUMAN; INFANT; KARYOTYPE; MALE; PRIORITY JOURNAL;

EID: 0033582940     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990319)83:3<201::AID-AJMG11>3.0.CO;2-V     Document Type: Article

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