GENETIC-LINKAGE STUDIES IN ALZHEIMERS-DISEASE FAMILIES

[1] A NEW PROBE FOR THE DIAGNOSIS OF MYOTONIC MUSCULAR-DYSTROPHY [J]. SCIENCE, 1987, 235 (4796) : 1648 - 1650

[2] BIRD TD, 1982, AM J HUM GENET, V34, P388

[3] GENETIC-LINKAGE EVIDENCE FOR HETEROGENEITY IN CHARCOT-MARIE-TOOTH NEUROPATHY (HMSN TYPE-I) [J]. ANNALS OF NEUROLOGY, 1983, 14 (06) : 679 - 684

[4] BOEHNKE M, 1986, AM J HUM GENET, V39, P513

[5] BREITNER JCS, 1988, NEUROLOGY, V38, P207

[6] FAMILIAL ALZHEIMER DEMENTIA - A PREVALENT DISORDER WITH SPECIFIC CLINICAL-FEATURES [J]. PSYCHOLOGICAL MEDICINE, 1984, 14 (01) : 63 - 80

[7] CAVALLISFORZA SF, 1971, GENETICS HUMAN POPUL

[8] CHOMCZYNSKI P, 1985, ALKALINE TRANSFER DN

[9] NEUROOPHTHALMOLOGICAL FINDINGS IN VESTIBULOCEREBELLAR ATAXIA [J]. ARCHIVES OF NEUROLOGY, 1986, 43 (10) : 1050 - 1053

[10] NEUROPSYCHOLOGICAL FEATURES OF EARLY-ONSET AND LATE-ONSET ALZHEIMERS-DISEASE [J]. ARCHIVES OF NEUROLOGY, 1986, 43 (06) : 574 - 576

[1] A NEW PROBE FOR THE DIAGNOSIS OF MYOTONIC MUSCULAR-DYSTROPHY [J]. SCIENCE, 1987, 235 (4796) : 1648 - 1650

[2] BIRD TD, 1982, AM J HUM GENET, V34, P388

[3] GENETIC-LINKAGE EVIDENCE FOR HETEROGENEITY IN CHARCOT-MARIE-TOOTH NEUROPATHY (HMSN TYPE-I) [J]. ANNALS OF NEUROLOGY, 1983, 14 (06) : 679 - 684

[4] BOEHNKE M, 1986, AM J HUM GENET, V39, P513

[5] BREITNER JCS, 1988, NEUROLOGY, V38, P207

[6] FAMILIAL ALZHEIMER DEMENTIA - A PREVALENT DISORDER WITH SPECIFIC CLINICAL-FEATURES [J]. PSYCHOLOGICAL MEDICINE, 1984, 14 (01) : 63 - 80

[7] CAVALLISFORZA SF, 1971, GENETICS HUMAN POPUL

[8] CHOMCZYNSKI P, 1985, ALKALINE TRANSFER DN

[9] NEUROOPHTHALMOLOGICAL FINDINGS IN VESTIBULOCEREBELLAR ATAXIA [J]. ARCHIVES OF NEUROLOGY, 1986, 43 (10) : 1050 - 1053

[10] NEUROPSYCHOLOGICAL FEATURES OF EARLY-ONSET AND LATE-ONSET ALZHEIMERS-DISEASE [J]. ARCHIVES OF NEUROLOGY, 1986, 43 (06) : 574 - 576