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Showing articles 0 to 8 of 8 Filter Applied: cerebellar hypoplasia (Click to remove) Oligophrenin 1 Mutations Frequently Cause X-Linked Mental Retardation with Cerebellar Hypoplasia Neurol 65:1364-1369,1346, Zanni,G.,et al, 2005 Bilat Periventricular Nodular Heterotopia with Mental Retard & Syndactyly in Boys:New X-Linked MR Synd Neurol 49:1042-1047, Dobyns,W.B.,et al, 1997 Congenital Lymphocytic Choriomeningitis Virus Infection: Spectrum of Disease Ann Neurol 62:347-355, Bonthius,D.J.,et al, 2007 Ataxia with Aniridia of Gillespie:A Case Report Neurol 31:95-97, Lechtenberg,R.,et al, 1981 Human Cerebellar Hypoplasia, A Syndrome of Diverse Causes Arch Neurol 37:300-305, Sarnatt,H.B.,et al, 1980 Neuroanatomy of Fragile X Syndrome:The Posterior Fossa Ann Neurol 29:26-32, Reiss,A.L.,et al, 1991 Magnetic Resonance Imaging of the Brain in Congenital Rubella Virus and Cytomegalovirus Infections Neuroradiology 33:239-242, Sugita,K.,et al, 1991 Leber's Congenital Amaurosis Arch Neurol 41:204-206, Weinstein,J.M.,et al, 1984 Showing articles 0 to 8 of 8