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Texas Heart Institute Journal|January 1, 1997
Outcomes among pediatric heart transplant recipientsR J Gajarski, H M Rosenblatt, S W Denfield, et al.
Obstetrics and Gynecology|August 29, 1998
Intrauterine viral infection at the time of second trimester genetic amniocentesisK D Wenstrom, W W Andrews, N E Bowles, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|September 25, 2004
A family-based association study of congenital left-sided heart malformations and 5,10 methylenetetrahydrofolate reductaseKim L McBride, Susan Fernbach, Andres Menesses, et al.
Molecular Genetics and Metabolism|June 8, 2002
Compound heterozygous mutations in KvLQT1 cause Jervell and Lange-Nielsen syndromeZhiqing Wang, Hua Li, Arthur J Moss, et al.
The American Journal of Cardiology|January 1, 1995
Differentiating anomalous left main coronary artery originating from the pulmonary artery in infants from myocarditis and dilated cardiomyopathy by electrocardiogramC L Johnsrude, J C Perry, F Cecchin, et al.
Pediatric Radiology|July 15, 1998
Percutaneous gastrostomy tube placement in patients with ventriculoperitoneal shuntsS S Sane, A Towbin, E A Bergey, et al.
Pharmacotherapy|February 10, 2006
Administration of a large nesiritide bolus dose in a pediatric patient: case report and review of nesiritide use in pediatricsBrady S Moffett, John L Jefferies, Jack F Price, et al.
The Journal of Heart and Lung Transplantation : the Official Publication of the International Society for Heart Transplantation|February 17, 2018
Cardiac transplantation in children with Down syndrome, Turner syndrome, and other chromosomal anomalies: A multi-institutional outcomes analysisChristopher R Broda, Antonio G Cabrera, Joseph W Rossano, et al.
Pacing and Clinical Electrophysiology : PACE|September 2, 2009
A nonsense SCN5A mutation associated with Brugada-type electrocardiogram and intraventricular conduction defectsKaveh Samani, Tomohiko Ai, Jeffrey A Towbin, et al.
American Journal of Human Genetics|November 1, 1990
Deletion mapping of Aland Island eye disease to Xp21 between DXS67 (B24) and Duchenne muscular dystrophyD A Pillers, J A Towbin, J S Chamberlain, et al.
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