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Showing articles 0 to 4 of 4 Filter Applied: chromosomal abnormality (Click to remove) Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Neuroblastoma -- from Genetic Profiles to Clinical Challenge NEJM 353:2215-2217, Kushner,B.H. &Cheung,N.-K.V., 2005 Brain Tumors NEJM 324:1471-1476, 1555-15641991., Black,P.McL., 1991 Showing articles 0 to 4 of 4