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The Yale Journal of Biology and Medicine|September 1, 1981
Knowledge and attitudes toward Tay-Sachs disease among a college student populationC F Austein, M R Seashore, S S MickAmerican Journal of Medical Genetics|June 14, 1996
A-2-->G transition at the 3' acceptor splice site of IVS17 characterizes the COL2A1 gene mutation in the original Stickler syndrome kindredC J Williams, A Ganguly, E Considine, et al.Pediatrics|February 1, 1985
Loss of intellectual function in children with phenylketonuria after relaxation of dietary phenylalanine restrictionM R Seashore, E Friedman, R A Novelly, et al.Journal of Medical Genetics|October 1, 1981
Complete trisomy 9 in two liveborn infantsS Mantagos, J W McReynolds, M R Seashore, et al.Pediatrics|December 10, 1999
Development of guidelines for treatment of children with phenylketonuria: report of a meeting at the National Institute of Child Health and Human Development held August 15, 1995, National Institutes of Health, Bethesda, MarylandM R Seashore, R Wappner, S Cho, et al.Pediatrics|December 10, 1999
Management of phenylketonuria for optimal outcome: a review of guidelines for phenylketonuria management and a report of surveys of parents, patients, and clinic directorsR Wappner, S Cho, R A Kronmal, et al.The Yale Journal of Biology and Medicine|January 1, 1990
Idiopathic Fanconi syndrome with progressive renal failure: a case report and discussionW S Long, M R Seashore, N J Siegel, et al.Pediatrics|October 1, 1987
Familial apple peel jejunal atresia: surgical, genetic, and radiographic aspectsJ H Seashore, F S Collins, R I Markowitz, et al.Breast Cancer Research and Treatment|January 14, 2000
p73 mutations are not detected in sporadic and hereditary breast cancerD I Schwartz, N M Lindor, C Walsh-Vockley, et al.Obstetrics and Gynecology|June 1, 1988
Prenatal findings in a case of spondylocostal dysplasia type I (Jarcho-Levin syndrome)R Romero, A Ghidini, M S Eswara, et al.Pageof 4