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Showing articles 0 to 8 of 8 Filter Applied: chromosomal abnormality (Click to remove) A Middle-aged Woman with Severe Scoliosis and Encephalopathy JAMA Neurol 78:251-252, Mohan, G.,et al, 2021 Clinical Spectrum of Mutations in SCN1A Gene: Severe Myoclonic Epilepsy in Infancy and Related Epilepsies Epilepsy Res 70S:S223-S230, Fujiwara,T., 2006 Genetic, Clinical, and Radiographic Delineation of Hallervorden-Spatz Syndrome NEJM 348:33-40, Hayflick,S.J.,et al, 2003 Learning Disability Lancet 362:811-821, Gillberg,C.&Soderstrom,H., 2003 Intelligence and the X Chromosome Lancet 347:1814-1815, Turner,G., 1996 X-Chromosome Effects on Female Brain:A Magnetic Resonance Imaging Study of Turner's Syndrome Lancet 342:1197-1200, Murphy,D.G.M.,et al, 1993 Girls with Fragile X Syndrome:Physical and Neurocognitive Status and Outcome Pediatrics 89:395-400, Hagerman,R.J.,et al, 1992 Wilson Disease Medicine 71:139-164, Brewer,G.J.&Yuzbasiyan-Gurkan,V., 1992 Showing articles 0 to 8 of 8