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Showing articles 0 to 7 of 7 Filter Applied: chromosomal abnormality (Click to remove) CNS Involvement at the Onset of Primary Hemophagocytic Lymphohistiocytosis Neurol 78:1150-1156, Deiva,K.,et al, 2012 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Autosomal Dominant Migraine with MRI White-Matter Abnormalities Mapping to the CADASIL Locus Neurol 45:1086-1091, Chabriat,H.,et al, 1995 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 New Phenotype of the Cerebral Autosomal Dominant Arteriopathy Mapped to Chromosome 19:Migraine as the Prominent Clinical Feature JNNP 59:579-585, Verin,M.,et al, 1995 Cockayne Syndrome: Review of 140 Cases Am J Med Genet 42:68-84, Nance,M.A. &Berry,S.A., 1992 Physical Features of Prader-Willi Syndrome in Neonates Am J Dis Child 144:1251-1254, Aughton,D.J.&Cassidy,S.B., 1990 Showing articles 0 to 7 of 7