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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 20, 2025. (Total: 235500Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hypoplastic Left Heart Syndrome and NKX2-5[original query]
Cardiac homeobox gene NKX2-5 mutations and congenital heart disease: associations with atrial septal defect and hypoplastic left heart syndrome.
Journal of the American College of Cardiology 2003 Jun 41 (11): 2072-6.
Elliott David A, Kirk Edwin P, Yeoh Thomas, Chandar Suchitra, McKenzie Fiona, Taylor Peter, Grossfeld Paul, Fatkin Diane, Jones Owen, Hayes Peter, Feneley Michael, Harvey Richard
Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease.
Clinical genetics 2010 Dec 78 (6): 533-40.
Stallmeyer B, Fenge H, Nowak-Göttl U, Schulze-Bahr
Genetic abnormalities in FOXP1 are associated with congenital heart defects.
Human mutation 2013 Sep 34 (9): 1226-30.
Chang Sheng-Wei, Mislankar Mona, Misra Chaitali, Huang Nianyuan, Dajusta Daniel G, Harrison Steven M, McBride Kim L, Baker Linda A, Garg Vi
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