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Showing articles 0 to 8 of 8 Filter Applied: genetic screening (Click to remove) The Spectrum of Fragile X Disorders NEJM 393:281-288, Hagerman,R.H. & Hagerman,P.J., 2025 Spinal Muscular Atrophy UpToDate, Oct, Bodamer,O.A., 2022 Range of Genetic Mutations Associated with Severe Non-Syndromic Sporadic Intellectual Disability: An Exome Sequencing Study Lancet 380:1674-1682, Rauch, A.,et al, 2012 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 Penetrance of the Fragile X-Associated Tremor/Ataxia Syndrome in a Premutation Carrier Population JAMA 291:460-469, Jacquemont,S.,et al, 2004 Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era JAMA 270:2307-2315, Kaback,M.,et al, 1993 Screening for Carriers of Tay-Sachs Disease Among Ashkenazi Jews NEJM 323:6-12, Triggs-Raine,B.L.,et al, 1990 Amaurotic Family Idiocy Am J Dis Child 142:53-56, Abt,I.A., 1988 Showing articles 0 to 8 of 8