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Showing articles 0 to 11 of 11 Filter Applied: chromosomal abnormality (Click to remove) The Epilepsy of Trisomy 9p Neurol 47:821-824, Stern,J.M., 1996 Clinical and Genetic Abnormalities in Patients with Friedreich's Ataxia NEJM 335:1169-1175, 12221996., Durr,A.,et al, 1996 Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Angelman Syndrome: Clinical Profile J Child Neurol 7:270-280, Zori,R.T.,et al, 1992 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Fucosidosis Revisited:A Review of 77 Patients Am J Med Genet 38:111-131, Willems,P.J.,et al, 1991 Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Agenesis of the Corpus Callosum:A Study of the Frequency of Associated Malformations Ann Neurol 6:349-354, Parrish,M.L.,et al, 1979 The Cornelia de Lange Syndrome J Pediatr 63:1000-1020, Ptacek,L.J., 1963 Showing articles 0 to 11 of 11