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Showing articles 0 to 8 of 8 Filter Applied: genetic screening (Click to remove) Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Spinal Muscular Atrophy UpToDate, Oct, Bodamer,O.A., 2022 Hereditary Spastic Paraplegia:From Diagnosis to Emerging Therapeutic Approaches Lancet Neurol 18:1136-1146, Shribman,S.,et al, 2019 Disclosure of APOE Genotype for Risk of Alzheimers Disease NEJM 361:245-254,298, Green,R.C.,et al, 2009 The Tuberous Sclerosis Complex NEJM 355:1345-1356, Crino,P.B.,et al, 2006 A Simplified Six-Item Checklist for Screening for Fragile X Syndrome in the Pediatric Population J Pediatr 129:611-614, Giangreco,C.A.,et al, 1996 Clinical Spectrum of CADASIL:A Study of 7 Families Lancet 346:934-939, Chabriat,H.,et al, 1995 Showing articles 0 to 8 of 8