Spinal Muscular Atrophy
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Adrenoleukodystrophy
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The Clinical Introduction of Genetic Testing for Alzheimer Disease, An Ethical Perspective
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Statement of Use of Apolipoprotein E Testing for Alzheimer Disease
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The Cerebral Autosomal-Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) Scale
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Cerebral Autosomal Dominant Arteriopathy With Subcortical Infarcts & Leukoencephalopathy (CADASIL)
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The Tuberous Sclerosis Complex
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Few Psychological Consequences of Presymptomatic Testing for Huntington Disease
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Apolipoprotein E Genotyping in Alzheimer's Disease
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Genetic Factors in Alzheimer's Disease:A Review of Recent Advances
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Practice Parameter:Genetic Testing Alert
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Presymptomatic Diagnosis of Neurofibromatosis 2 Using Linked Genetic Markers, Neuroimging, and Ocular Examinations
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Clinical Spectrum of CADASIL:A Study of 7 Families
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A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
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Experience with Screening Newborns for Duchenne Muscular Dystrophy in Wales
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Rapid Fragile X Carrier Screening and Prenatal Diagnosis Using a Nonradioactive PCR Test
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Tay-Sachs Disease-Carrier Screening, Prenatal Diagnosis, and the Molecular Era
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Population Screening for Fragile X
Lancet 339:1210-1213, Turner,G.,et al, 1992
The Psychological Consequences of Predictive Testing for Huntington's Disease
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Genetic Testing for Huntington's Disease
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Predictive Testing for Huntington's Disease, Progress and Problems
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Gene Studies in Newborn Males with Duchenne Muscular Dystrophy Detected by Neonatal Screening
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Preventive Screening for Fragile X Syndrome
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