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Showing articles 0 to 12 of 12 Filter Applied: genetic linkage (Click to remove) Association of HTRA1 Mutations and Familial Ischemic Cerebral Small-Vessel Disease NEJM 360:1729-1739, Hara,K.,et al, 2009 New Players in the Genetics of Stroke NEJM 347:1711-1712, Tournier-Lasserve,E., 2002 Strong Clustering and Stereotyped Nature of Notch3 Mutations, in CADASIL Patients Lancet 350:1511-1515, 14901997., Joutel,A.,et al, 1997 Von Hippel-Lindau Disease Affecting 43 Members of a Single Kindred Medicine 68:1-29, Lamiell,J.M.,et al, 1989 Linkiage of Locus for Cerebral Cavernous Hemagiomas to Chromosome 7q in 4 Families of Mexican-American Descent Neurol 48:752-757, Polymeropoulos,M.H.,et al, 1997 Misdiagnosis Revealed by Genetic Linkage Analysis in a Family with Wilson Disease Neurol 46:1485-1486, Vidaud,D.,et al, 1996 Molecular Genetics in Neurology Ann Neurol 34:757-773, Martin,J.B., 1993 Prenatal Diagnosis of Wilson's Disease by Analysis of DNA Polymorphism NEJM 327:57, Cossu,P.,et al, 1992 Brief Report:Intragenic Deletion of the Kalig-1 Gene in Kallmann's Syndrome NEJM 326:1752-1755, 17751992., Bick,D.,et al, 1992 Central Nervous System Lesions in von Hippel-Lindau Syndrome JNNP 55:898-901, Neumann,H.P.H.,et al, 1992 Predictive Testing for Wilson's Disease Using Tightly Linked and Flanking DNA Markers Neurol 41:992-999, Farrer,L.A.,et al, 1991 Homing in on Wilson's Disease Editorial, Lancet 1:822-8231989., , 1989 Showing articles 0 to 12 of 12