-
2
-
-
0018134793
-
Dominant spino-pontine atrophy: Report of two additional members of the family W
-
Pogacar, S. et al. Dominant spino-pontine atrophy: Report of two additional members of the family W. Arch. Neurol. 35, 156-162 (1978).
-
(1978)
Arch. Neurol
, vol.35
, pp. 156-162
-
-
Pogacar, S.1
-
3
-
-
0001689838
-
On hereditary ataxy, with a series of twenty-one cases
-
Brown, S. On hereditary ataxy, with a series of twenty-one cases. Brain15, 250-268 (1982).
-
(1982)
Brain
, vol.15
, pp. 250-268
-
-
Brown, S.1
-
4
-
-
0015007562
-
Dominant olivo-ponto-cerebellar atrophy with extrapyramidal signs. Report of a family through three generations
-
Konigsmark, B.W. & Lipton, H.L. Dominant olivo-ponto-cerebellar atrophy with extrapyramidal signs. Report of a family through three generations. Birth Defects Orig. Art. Ser. 1, 178-191 (1971).
-
(1971)
Birth Defects Orig. Art. Ser
, vol.1
, pp. 178-191
-
-
Konigsmark, B.W.1
Lipton, H.L.2
-
5
-
-
0014072533
-
Hereditary olivo-ponto-cerebellar atrophy with retinal degeneration. Report of a family through six generations
-
Weiner, L.P., Konigsmark, B.W., Stoll, J.Jr. & Magladery, J.W. Hereditary olivo-ponto-cerebellar atrophy with retinal degeneration. Report of a family through six generations. Arch. Neurol. 16, 364-376 (1967).
-
(1967)
Arch. Neurol
, vol.16
, pp. 364-376
-
-
Weiner, L.P.1
Konigsmark, B.W.2
Stoll, J.3
Magladery, J.W.4
-
6
-
-
0026849567
-
Positional cloning: Let's not call it reverse anymore
-
Collins, F.S. Positional cloning: Let's not call it reverse anymore. Nature Genet. 1, 3-6 (1992).
-
(1992)
Nature Genet
, vol.1
, pp. 3-6
-
-
Collins, F.S.1
-
7
-
-
0016396382
-
Hereditary ataxia and HLA genotypes
-
Yakura, H., Wakisaka, A., Fujimotos, S. & Itakura, K. Hereditary ataxia and HLA genotypes. New Engl. J. Med. 291, 154-155 (1974).
-
(1974)
New Engl. J. Med
, vol.291
, pp. 154-155
-
-
Yakura, H.1
Wakisaka, A.2
Fujimotos, S.3
Itakura, K.4
-
8
-
-
0017389522
-
Spinocerebellar ataxia and HLA linkage: Risk prediction by HLA typing
-
Jackson, J.F., Currier, R.D., Terasaki, P.I. & Morton, N.E. Spinocerebellar ataxia and HLA linkage: Risk prediction by HLA typing. New Engl. J. Med.296, 1138-1141 (1977).
-
(1977)
New Engl. J. Med
, vol.296
, pp. 1138-1141
-
-
Jackson, J.F.1
Currier, R.D.2
Terasaki, P.I.3
Morton, N.E.4
-
9
-
-
0025339987
-
Dinucleotide polymorphism at the D6S89 locus
-
Litt, M. & Luty, J.A. Dinucleotide polymorphism at the D6S89 locus. Nucl. Acids Res. 18, 4301 (1990).
-
(1990)
Nucl. Acids Res
, vol.18
, pp. 4301
-
-
Litt, M.1
Luty, J.A.2
-
10
-
-
0026097010
-
Dinucleotide repeat polymorphism at the D6S109 locus
-
Ranum, L., Chung, M.Y., Duvick, L.A., Zoghbi, H.Y. & Orr, H.T. Dinucleotide repeat polymorphism at the D6S109 locus. Nucl. Acids Res.19, 1171 (1991).
-
(1991)
Nucl. Acids Res
, vol.19
, pp. 1171
-
-
Ranum, L.1
Chung, M.Y.2
Duvick, L.A.3
Zoghbi, H.Y.4
Orr, H.T.5
-
11
-
-
0024997225
-
Autosomal dominant cerebellar ataxia: Clinical analysis of 263 patients from a homogeneous population in Holguin, Cuba
-
Orozco, G., Nodarse, A., Cordoves, R. & Auburger, G. Autosomal dominant cerebellar ataxia: Clinical analysis of 263 patients from a homogeneous population in Holguin, Cuba. Neurology 40, 1369-1375 (1990).
-
(1990)
Neurology
, vol.40
, pp. 1369-1375
-
-
Orozco, G.1
Nodarse, A.2
Cordoves, R.3
Auburger, G.4
-
12
-
-
0025350263
-
Autosomal dominant ataxia: Genetic evidence for locus heterogeneity from a Cuban founder effect population
-
Auburger, G. et al. Autosomal dominant ataxia: Genetic evidence for locus heterogeneity from a Cuban founder effect population. Am. J. hum. Genet. 46, 1163-1177 (1990).
-
(1990)
Am. J. Hum. Genet
, vol.46
, pp. 1163-1177
-
-
Auburger, G.1
-
13
-
-
0026132133
-
Guidelines for human linkage maps: An international system for human linkage maps (ISLM, 1990)
-
Keats, B.J.B. et al. Guidelines for human linkage maps: An international system for human linkage maps (ISLM, 1990). Genomics 9, 557-560 (1991).
-
(1991)
Genomics
, vol.9
, pp. 557-560
-
-
Keats, B.J.B.1
-
14
-
-
0022001611
-
The human gene encoding insulin-like growth factor I is located on chromosome 12
-
Hoppener, J.W. et al. The human gene encoding insulin-like growth factor I is located on chromosome 12. Hum. Genet. 69, 157-160 (1985).
-
(1985)
Hum. Genet
, vol.69
, pp. 157-160
-
-
Hoppener, J.W.1
-
15
-
-
84901967388
-
In Human Gene Mapping 11. Report of the committee on the genetic constitution of chromosome 12
-
[A26934]
-
Weber, J.L., Kwitek, A.E., May, P.E., Wilkie, P.J. & Decker, R.A. In Human Gene Mapping 11. Report of the committee on the genetic constitution of chromosome 12. Cytogenet. cell Genet. 58, 555-579 [A26934] (1991).
-
(1991)
Cytogenet. Cell Genet
, vol.58
, pp. 555-579
-
-
Weber, J.L.1
Kwitek, A.E.2
May, P.E.3
Wilkie, P.J.4
Decker, R.A.5
-
16
-
-
0017689205
-
Azorean disease of the nervous system
-
Romanul, F.C.A., Fowler, H.L., Radvany, J., Feldman, R.G. & Feingold, M. Azorean disease of the nervous system. New Engl. J. Med. 296, 1505-1508 (1977).
-
(1977)
New Engl. J. Med
, vol.296
, pp. 1505-1508
-
-
Romanul, F.C.A.1
Fowler, H.L.2
Radvany, J.3
Feldman, R.G.4
Feingold, M.5
-
17
-
-
0017871680
-
Autosomal dominant system degeneration in Portuguese families of the Azores Islands: A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions
-
Coutinho, P. & Andrade, C. Autosomal dominant system degeneration in Portuguese families of the Azores Islands: A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions. Neurol. 28, 703-709 (1978).
-
(1978)
Neurol
, vol.28
, pp. 703-709
-
-
Coutinho, P.1
Andrade, C.2
-
18
-
-
0027409777
-
Search of the chromosome locus of autosomal dominant cerebellar ataxia from Holguin, Cuba: Exclusion from candidate regions on chromosome 4 and 11q
-
Gispert, S., Nothers, C., Orozco, G. & Auburger, G. Search of the chromosome locus of autosomal dominant cerebellar ataxia from Holguin, Cuba: Exclusion from candidate regions on chromosome 4 and 11q. Hum. Heredity 43, 12-30 (1993).
-
(1993)
Hum. Heredity
, vol.43
, pp. 12-30
-
-
Gispert, S.1
Nothers, C.2
Orozco, G.3
Auburger, G.4
-
19
-
-
84970055409
-
Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1. Clinical and genetic analysis of 10 French families
-
(in the press)
-
Khati, C. et al. Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1. Clinical and genetic analysis of 10 French families.Neurology (in the press).
-
Neurology
-
-
Khati, C.1
-
20
-
-
0024582686
-
Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction
-
Weber, J.L. & May, P.E. Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. Am. J. hum. Genet. 44, 388-396 (1989).
-
(1989)
Am. J. Hum. Genet
, vol.44
, pp. 388-396
-
-
Weber, J.L.1
May, P.E.2
-
21
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
Lathrop, G.M., Lalouel, J.M., Julier, C. & Ott, J. Strategies for multilocus linkage analysis in humans. Proc. natn. Acad. Sci. U.S.A. 81, 3443-3446 (1984).
-
(1984)
Proc. Natn. Acad. Sci. U.S.A
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
22
-
-
0018570972
-
Genetic linkage studies in man
-
Ott, J. Genetic linkage studies in man. Transplant. Proc. XI, 1689-91 (1979).
-
(1979)
Transplant. Proc
, vol.11
, pp. 1689-1691
-
-
Ott, J.1
-
23
-
-
0025648765
-
Trinucleotide repeat polymorphism at the human pancreatic phospholipase A-2 gene (PLA2)
-
Polymeropoulos, M.H., Rath, D.S., Xiao, H. & Merril, C.R. Trinucleotide repeat polymorphism at the human pancreatic phospholipase A-2 gene (PLA2). Nucl. Acids Res. 18, 7468 (1990).
-
(1990)
Nucl. Acids Res
, vol.18
, pp. 7468
-
-
Polymeropoulos, M.H.1
Rath, D.S.2
Xiao, H.3
Merril, C.R.4
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