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MESP1 Mutations in Patients with Congenital Heart Defects.
Werner P, Latney B, Deardorff MA, Goldmuntz E. Werner P, et al. Among authors: goldmuntz e. Hum Mutat. 2016 Mar;37(3):308-14. doi: 10.1002/humu.22947. Epub 2016 Jan 19. Hum Mutat. 2016. PMID: 26694203 Free PMC article.
NKX2.5 mutations in patients with congenital heart disease.
McElhinney DB, Geiger E, Blinder J, Benson DW, Goldmuntz E. McElhinney DB, et al. Among authors: goldmuntz e. J Am Coll Cardiol. 2003 Nov 5;42(9):1650-5. doi: 10.1016/j.jacc.2003.05.004. J Am Coll Cardiol. 2003. PMID: 14607454 Free article.
Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Pierpont ME, Basson CT, Benson DW Jr, Gelb BD, Giglia TM, Goldmuntz E, McGee G, Sable CA, Srivastava D, Webb CL; American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young. Pierpont ME, et al. Among authors: goldmuntz e. Circulation. 2007 Jun 12;115(23):3015-38. doi: 10.1161/CIRCULATIONAHA.106.183056. Epub 2007 May 22. Circulation. 2007. PMID: 17519398 Review.
GATA4 sequence variants in patients with congenital heart disease.
Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E. Tomita-Mitchell A, et al. Among authors: goldmuntz e. J Med Genet. 2007 Dec;44(12):779-83. doi: 10.1136/jmg.2007.052183. J Med Genet. 2007. PMID: 18055909 Free PMC article.
271 results