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Showing articles 0 to 8 of 8 Filter Applied: karyotyping (Click to remove) A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig Neurol 42:2251-2257, Mikati,M.A.,et al, 1992 Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992 Causal Heterogeneity in Isolated Lissencephaly Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992 Inherited Multiple Meningiomas:A Clinical, Pathological & Cytogenetic Study of an Affected Family JNNP 49:362-368, Battersby,R.D.E.,et al, 1986 Preventive Screening for Fragile X Syndrome Editorial, Lancet 2:1191-11921986., , 1986 Neurological Findings in Patients with the Fragile-X Syndrome JNNP 48:150-153, Finelli,P.F.,et al, 1985 Fragile X Chromosome & X-Linked Mental Retardation CMA Journal 127:123-126, Larbrisseau,A.,et al, 1982 Heterozygous Expression Of X-Linked Mental Retardation & X-chromosome Marker fra (X) (q27) NEJM 303:662-664, Turner,G.,et al, 1980 Showing articles 0 to 8 of 8