Enter your terms above and click the 'Search' button.

Showing articles 0 to 11 of 11 Filter Applied: genetic diagnosis,prenatal (Click to remove) Huntingtons Disease BMJ 341:34-40, Novak,M.J. &Tabrizi,S.J., 2010 Aicardi-Gouti�res Syndrome Br Med Bull 89:183-201, Orcesi, S.,et al, 2009 Molybdenum Cofactor Deficiency Neurol 85:e175-e178, Nagappa, M.,et al, 2015 Adrenoleukodystrophy JAMA 294:3131-3134, Moser,H.W.,et al, 2005 Prenatal Diagnosis Requests for Huntington's Disease when the Father is at Risk, and Does Not Want to Know His Genetic Status: Clinical, Legal, and Ethical Viewpoints BMJ 326:331-333, Tassicker,R.,et al, 2003 Advances in Molecular Analysis of Fragile X Syndrome 552, Warren,W.T.&Nelson,D.L.JAMA 271:536-553, 1994 Predictive Testing for Huntington's Disease with Linked DNA Markers Lancet 2:463-466, Brock,D.J.H.,et al, 1989 Uptake of Presymptomatic Predictive Testing for Huntington's Disease Lancet 2:603-605, Craufurd,D.,et al, 1989 Predictive Testing for Huntington's Disease with Use of a Linked DNA Marker NEJM 318:535-542, Meissen,G.J.,et al, 1988 The Peroxisome:Nervous System Role of a Previously Underrated Organelle, The 1987 Robert Wartenberg Lecture Neurol 38:1617-1627, Moser,H.W., 1988 First-Trimester Prenatal Diagnosis for Huntington's Disease with DNA Probes et al Lancet 1:1284-1285, Hayden,M.R., 1987 Showing articles 0 to 11 of 11