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Showing articles 0 to 8 of 8 Filter Applied: karyotyping (Click to remove) Causal Heterogeneity in Isolated Lissencephaly Neurol 42:1375-1388, Dobyns,W.B.,et al, 1992 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 The Epilepsy of Trisomy 9p Neurol 47:821-824, Stern,J.M., 1996 Population Screening for Fragile X Lancet 339:1210-1213, Turner,G.,et al, 1992 A Synd of Autosomal Dominant Alternating Hemiplegia:Mimicking Intractable Epilepsy; Chromosomal Studies; Physiol Investig Neurol 42:2251-2257, Mikati,M.A.,et al, 1992 Preventive Screening for Fragile X Syndrome Editorial, Lancet 2:1191-11921986., , 1986 Pediatric Neurology Psych Annals 2:1, , 1972 Showing articles 0 to 8 of 8