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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 13, 2020
22q11.2 deletion syndrome and congenital heart diseaseElizabeth GoldmuntzPediatric Clinics of North America|November 25, 2004
The genetic contribution to congenital heart diseaseElizabeth GoldmuntzMethods in Molecular Medicine|August 26, 2006
The cardiovascular manifestations of Alagille syndrome and JAGI mutationsElizabeth Goldmuntz, Elizabeth Moore, Nancy B SpinnerCardiology in the Young|November 15, 2021
Reported practice patterns in the ambulatory care setting for patients with CHDElizabeth Goldmuntz, Zihe Zheng, Judy A SheaCurrent Cardiology Reports|December 18, 2001
Genetic counseling for congenital heart disease: new approaches for a new decadeKaty Hoess, Elizabeth Goldmuntz, Reed E PyeritzBirth Defects Research. Part A, Clinical and Molecular Teratology|January 22, 2011
NAT1, NOS3, and TYMS genotypes and the risk of conotruncal cardiac defectsPhilip J Lupo, Laura E Mitchell, Elizabeth GoldmuntzJournal of Biomedicine & Biotechnology|January 30, 2010
Gene-gene interactions in the folate metabolic pathway and the risk of conotruncal heart defectsPhilip J Lupo, Elizabeth Goldmuntz, Laura E MitchellWorld Journal for Pediatric & Congenital Heart Surgery|June 27, 2013
Genetic testing in congenital heart disease: ethical considerationsKimberly Y Lin, Lisa C A D'Alessandro, Elizabeth GoldmuntzHuman Mutation|December 24, 2015
MESP1 Mutations in Patients with Congenital Heart DefectsPetra Werner, Brande Latney, Matthew A Deardorff, et al.Pageof 18