-
1
-
-
0025183708
-
Basic local alignment search tool
-
Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ (1990) Basic local alignment search tool. J Mol Biol 215:403-410
-
(1990)
J Mol Biol
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
2
-
-
0021906904
-
Integration of a dominant selectable marker into human chromosomes and transfer of marked chromosomes to mouse cells by microcell fusion
-
Athwal RS, Smarsh M, Searle BM, Deo SS (1985) Integration of a dominant selectable marker into human chromosomes and transfer of marked chromosomes to mouse cells by microcell fusion. Somat Cell Mol Genet 11:177-187
-
(1985)
Somat Cell Mol Genet
, vol.11
, pp. 177-187
-
-
Athwal, R.S.1
Smarsh, M.2
Searle, B.M.3
Deo, S.S.4
-
3
-
-
0031683446
-
CAG repeat expansion in autosomal dominant familial spastic paraplegia: Novel expansion in a subset of patients
-
Benson K, Horwitz M, Wolff J, Friend K, Thompson E, White S, Richards R, Raskind W, Bird T (1998) CAG repeat expansion in autosomal dominant familial spastic paraplegia: novel expansion in a subset of patients. Hum Mol Genet 7:1779-1786
-
(1998)
Hum Mol Genet
, vol.7
, pp. 1779-1786
-
-
Benson, K.1
Horwitz, M.2
Wolff, J.3
Friend, K.4
Thompson, E.5
White, S.6
Richards, R.7
Raskind, W.8
Bird, T.9
-
4
-
-
0000818854
-
A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1
-
Breschel TS, McInnis MG, Margolis RL, Sirugo G, Corneliussen B, Simpson SG, McMahon FJ, MacKinnon DF, Xu JF, Pleasant N, Huo Y, Ashworth RG, Grundstrom C, Grundstrom T, Kidd KK, DePaulo JR, Ross CA (1997) A novel, heritable, expanding CTG repeat in an intron of the SEF2-1 gene on chromosome 18q21.1. Hum Mol Genet 6:1855-1863
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1855-1863
-
-
Breschel, T.S.1
McInnis, M.G.2
Margolis, R.L.3
Sirugo, G.4
Corneliussen, B.5
Simpson, S.G.6
McMahon, F.J.7
MacKinnon, D.F.8
Xu, J.F.9
Pleasant, N.10
Huo, Y.11
Ashworth, R.G.12
Grundstrom, C.13
Grundstrom, T.14
Kidd, K.K.15
DePaulo, J.R.16
Ross, C.A.17
-
5
-
-
0029737834
-
Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family
-
Bürger J, Metzke H, Paternotte C, Schilling F, Hazan J, Reis A (1996) Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family. Hum Genet 98:371-375
-
(1996)
Hum Genet
, vol.98
, pp. 371-375
-
-
Bürger, J.1
Metzke, H.2
Paternotte, C.3
Schilling, F.4
Hazan, J.5
Reis, A.6
-
6
-
-
13344270899
-
Friedreich's ataxia: Autosomal recessive disease caused by an intronic GAA triplet repeat expansion
-
Campuzano V, Montermini L, Molto MD, Pianese L, Cossee M, Cavalcanti F, Monros E, Rodius F, Duclos F, Monticelli A, Zara F, Canizares J, Koutnikova H, Bidichandani SI, Gellera C, Brice A, Trouillas P, De Michele G, Filla A, De Frutos R, Palau F, Patel PI, Di Donato S, Mandel J-L, Cocozza S, Koenig M, Pandolfo M (1996) Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271:1423-1427
-
(1996)
Science
, vol.271
, pp. 1423-1427
-
-
Campuzano, V.1
Montermini, L.2
Molto, M.D.3
Pianese, L.4
Cossee, M.5
Cavalcanti, F.6
Monros, E.7
Rodius, F.8
Duclos, F.9
Monticelli, A.10
Zara, F.11
Canizares, J.12
Koutnikova, H.13
Bidichandani, S.I.14
Gellera, C.15
Brice, A.16
Trouillas, P.17
De Michele, G.18
Filla, A.19
De Frutos, R.20
Palau, F.21
Patel, P.I.22
Di Donato, S.23
Mandel, J.-L.24
Cocozza, S.25
Koenig, M.26
Pandolfo, M.27
more..
-
8
-
-
16944364511
-
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
-
David G, Abbas N, Stevanin G, Dürr A, Yvert G, Cancel G, Weber C, Imbert G, Saudou F, Antoniou E, Drabkin H, Gemmill R, Giunti P, Benomar A, Wood N, Ruberg M, Agid Y, Mandel JL, Brice A (1997) Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nat Genet 17:65-70
-
(1997)
Nat Genet
, vol.17
, pp. 65-70
-
-
David, G.1
Abbas, N.2
Stevanin, G.3
Dürr, A.4
Yvert, G.5
Cancel, G.6
Weber, C.7
Imbert, G.8
Saudou, F.9
Antoniou, E.10
Drabkin, H.11
Gemmill, R.12
Giunti, P.13
Benomar, A.14
Wood, N.15
Ruberg, M.16
Agid, Y.17
Mandel, J.L.18
Brice, A.19
-
9
-
-
0029862031
-
Pure familial spastic paraplegia: Clinical and genetic analysis of nine Belgian pedigrees
-
De Jonghe P, Krols L, Michalik A, Hazan J, Smeyers G, Löfgren A, Weissenbach J, Martin JJ, Van Broeckhoven C (1996) Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees. Eur J Hum Genet 4:260-266
-
(1996)
Eur J Hum Genet
, vol.4
, pp. 260-266
-
-
De Jonghe, P.1
Krols, L.2
Michalik, A.3
Hazan, J.4
Smeyers, G.5
Löfgren, A.6
Weissenbach, J.7
Martin, J.J.8
Van Broeckhoven, C.9
-
10
-
-
6844239536
-
Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion
-
Del-Favero J, Krols L, Michalik A, Theuns J, Löfgren A, Goossens D, Wehnert A, Van den Bossche D, Van Zand K, Backhovens H, Regenmorter N van, Martin JJ, Van Broeckhoven C (1998) Molecular genetic analysis of autosomal dominant cerebellar ataxia with retinal degeneration (ADCA type II) caused by CAG triplet repeat expansion. Hum Mol Genet 7:177-186
-
(1998)
Hum Mol Genet
, vol.7
, pp. 177-186
-
-
Del-Favero, J.1
Krols, L.2
Michalik, A.3
Theuns, J.4
Löfgren, A.5
Goossens, D.6
Wehnert, A.7
Van Den Bossche, D.8
Van Zand, K.9
Backhovens, H.10
Van Regenmorter, N.11
Martin, J.J.12
Van Broeckhoven, C.13
-
11
-
-
0033580459
-
YAC fragmentation with repetitive and single copy sequences: Detailed physical mapping of the presenilin 1 gene on chromosome 14
-
Del-Favero J, Goossens D, Van den Bossche D, Van Broeckhoven C (1999) YAC fragmentation with repetitive and single copy sequences: detailed physical mapping of the presenilin 1 gene on chromosome 14. Gene 229:193-201
-
(1999)
Gene
, vol.229
, pp. 193-201
-
-
Del-Favero, J.1
Goossens, D.2
Van Den Bossche, D.3
Van Broeckhoven, C.4
-
12
-
-
8944250670
-
Hereditary spastic paraplegia: Advances in genetic research
-
Fink JK, Heinmann-Patterson T (1996) Hereditary spastic paraplegia: advances in genetic research. Neurology 46:1507-1515
-
(1996)
Neurology
, vol.46
, pp. 1507-1515
-
-
Fink, J.K.1
Heinmann-Patterson, T.2
-
13
-
-
0028868126
-
Autosomal dominant familial spastic paraplegia: Tight linkage to chromosome 15q
-
Fink JK, Wu CT, Jones SM, Sharp GB, Lange BM, Lesicki A, Reinglass T, Varvil T, Otterud B, Leppert M (1995) Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q. Am J Hum Genet 56:188-192
-
(1995)
Am J Hum Genet
, vol.56
, pp. 188-192
-
-
Fink, J.K.1
Wu, C.T.2
Jones, S.M.3
Sharp, G.B.4
Lange, B.M.5
Lesicki, A.6
Reinglass, T.7
Varvil, T.8
Otterud, B.9
Leppert, M.10
-
14
-
-
0026562884
-
Improved method for high efficiency transformation of intact yeast cells
-
Gietz D, St Jean A, Woods R, Schiestl R (1992) Improved method for high efficiency transformation of intact yeast cells. Nucleic Acids Res 20:1425-1428
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 1425-1428
-
-
Gietz, D.1
St Jean, A.2
Woods, R.3
Schiestl, R.4
-
15
-
-
0027363223
-
Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q
-
Hazan J, Lamy C, Melki J, Munnich A, Recondo J de, Weissenbach J (1993) Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q. Nat Genet 5:163-167
-
(1993)
Nat Genet
, vol.5
, pp. 163-167
-
-
Hazan, J.1
Lamy, C.2
Melki, J.3
Munnich, A.4
De Recondo, J.5
Weissenbach, J.6
-
16
-
-
0027981739
-
Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p
-
Hazan J, Fontaine B, Bruyn RP, Lamy C, Deutekom JC van, Rime CS, Dürr A, Melki J, Lyon-Caen O, Agid Y, Munnich A, Padberg GW, Recondo J de, Frants RR, Brice A, Weissenbach J (1994) Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p. Hum Mol Genet 3: 1569-1573
-
(1994)
Hum Mol Genet
, vol.3
, pp. 1569-1573
-
-
Hazan, J.1
Fontaine, B.2
Bruyn, R.P.3
Lamy, C.4
Van Deutekom, J.C.5
Rime, C.S.6
Dürr, A.7
Melki, J.8
Lyon-Caen, O.9
Agid, Y.10
Munnich, A.11
Padberg, G.W.12
De Recondo, J.13
Frants, R.R.14
Brice, A.15
Weissenbach, J.16
-
17
-
-
0031960716
-
Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p
-
Heinzlef O, Paternotte C, Mahieux F, Prudhomme JF, Dien J, Madigand M, Pouget J, Weissenbach J, Roullet E, Hazan J (1998) Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. J Med Genet 35:89-93
-
(1998)
J Med Genet
, vol.35
, pp. 89-93
-
-
Heinzlef, O.1
Paternotte, C.2
Mahieux, F.3
Prudhomme, J.F.4
Dien, J.5
Madigand, M.6
Pouget, J.7
Weissenbach, J.8
Roullet, E.9
Hazan, J.10
-
18
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
Huntington's Disease Collaborative Research Group (1993) A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. Cell 72:971-983
-
(1993)
Cell
, vol.72
, pp. 971-983
-
-
-
19
-
-
0030294345
-
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity of expanded CAG/glutamine repeats
-
Imbert G, Saudou F, Yvert G, Devys D, Trottier Y, Garnier JM, Weber C, Mandel JL, Cancel G, Abbas N, Dürr A, Didierjean O, Stevanin G, Agid Y, Brice A (1996) Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity of expanded CAG/glutamine repeats. Nat Genet 11:285-291
-
(1996)
Nat Genet
, vol.11
, pp. 285-291
-
-
Imbert, G.1
Saudou, F.2
Yvert, G.3
Devys, D.4
Trottier, Y.5
Garnier, J.M.6
Weber, C.7
Mandel, J.L.8
Cancel, G.9
Abbas, N.10
Dürr, A.11
Didierjean, O.12
Stevanin, G.13
Agid, Y.14
Brice, A.15
-
20
-
-
0028143527
-
CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1
-
Kawaguchi Y, Okamoto T, Taniwaki M, Aizawa M, Inoue M, Katayama S, Kawakami H, Nakamura S, Nishimura M, Akiguchi I, Kimura J, Narumiya S, Kkizuka A (1994) CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nat Genet 8:221-228
-
(1994)
Nat Genet
, vol.8
, pp. 221-228
-
-
Kawaguchi, Y.1
Okamoto, T.2
Taniwaki, M.3
Aizawa, M.4
Inoue, M.5
Katayama, S.6
Kawakami, H.7
Nakamura, S.8
Nishimura, M.9
Akiguchi, I.10
Kimura, J.11
Narumiya, S.12
Kkizuka, A.13
-
21
-
-
0028216760
-
Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA)
-
Koide R, Ikeuchi T, Onodera O, Tanaka H, Igarashi S, Endo K, Takahashi H, Kondo R, Ishikawa A, Hayashi T, Saito M, Tomoda A, Miike T, Naito H, Ikuta F, Tsuji S (1994) Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nat Genet 6:9-13
-
(1994)
Nat Genet
, vol.6
, pp. 9-13
-
-
Koide, R.1
Ikeuchi, T.2
Onodera, O.3
Tanaka, H.4
Igarashi, S.5
Endo, K.6
Takahashi, H.7
Kondo, R.8
Ishikawa, A.9
Hayashi, T.10
Saito, M.11
Tomoda, A.12
Miike, T.13
Naito, H.14
Ikuta, F.15
Tsuji, S.16
-
22
-
-
0031984597
-
Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA
-
Koob MD, Benzow KA, Bird TD, Day JW, Moseley ML, Ranum LPW (1998) Rapid cloning of expanded trinucleotide repeat sequences from genomic DNA. Nat Genet 18:72-75
-
(1998)
Nat Genet
, vol.18
, pp. 72-75
-
-
Koob, M.D.1
Benzow, K.A.2
Bird, T.D.3
Day, J.W.4
Moseley, M.L.5
Ranum, L.P.W.6
-
23
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada AR, Wilson EM, Lubahn DB, Harding AE, Fischbeck KH (1991) Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy. Nature 352:77-79
-
(1991)
Nature
, vol.352
, pp. 77-79
-
-
La Spada, A.R.1
Wilson, E.M.2
Lubahn, D.B.3
Harding, A.E.4
Fischbeck, K.H.5
-
24
-
-
0031439034
-
A CAG/CTG expansion in the normal population
-
Nakamoto M, Takebayashi H, Kawaguchi Y, Narumiya S, Taniwaki M, Nakamura Y, Ishikawa Y, Akiguchi I, Kimura J, Kakizuka A (1997) A CAG/CTG expansion in the normal population. Nat Genet 17:385-386
-
(1997)
Nat Genet
, vol.17
, pp. 385-386
-
-
Nakamoto, M.1
Takebayashi, H.2
Kawaguchi, Y.3
Narumiya, S.4
Taniwaki, M.5
Nakamura, Y.6
Ishikawa, Y.7
Akiguchi, I.8
Kimura, J.9
Kakizuka, A.10
-
25
-
-
0030807772
-
CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24
-
Nielsen JE, Koefoed P, Abell K, Hasholt L, Eiberg H, Fenger K, Niebuhr E, Sorensen S (1997) CAG repeat expansion in autosomal dominant pure spastic paraplegia linked to chromosome 2p21-p24. Hum Mol Genet 6:1811-1816
-
(1997)
Hum Mol Genet
, vol.6
, pp. 1811-1816
-
-
Nielsen, J.E.1
Koefoed, P.2
Abell, K.3
Hasholt, L.4
Eiberg, H.5
Fenger, K.6
Niebuhr, E.7
Sorensen, S.8
-
26
-
-
0027164698
-
Expansion on an unstable trinucleotide (CAG) repeat in spino-cerebellar ataxia type 1
-
Orr HT, Chung M, Banfi S, Kwiatkowski TJ, Servadio A, Beaudet AL, McCall AE, Duvick LA, Ranum LPW, Zoghbi HY (1993) Expansion on an unstable trinucleotide (CAG) repeat in spino-cerebellar ataxia type 1. Nat Genet 4:221-226
-
(1993)
Nat Genet
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.2
Banfi, S.3
Kwiatkowski, T.J.4
Servadio, A.5
Beaudet, A.L.6
McCall, A.E.7
Duvick, L.A.8
Ranum, L.P.W.9
Zoghbi, H.Y.10
-
27
-
-
0030292488
-
Moderate expansion of a normally bi-allelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst SM, Nechiporuk A, Nechiporuk T, Gispert S, Chen XN, Lopes-Cendes I, Pearlman S, Starkman S, Orozco-Diaz G, Lunkes A, DeJong P, Rouleau GA, Auburger G, Korenberg JR, Figueroa C, Sahba S (1996) Moderate expansion of a normally bi-allelic trinucleotide repeat in spinocerebellar ataxia type 2. Nat Genet 14:269-276
-
(1996)
Nat Genet
, vol.14
, pp. 269-276
-
-
Pulst, S.M.1
Nechiporuk, A.2
Nechiporuk, T.3
Gispert, S.4
Chen, X.N.5
Lopes-Cendes, I.6
Pearlman, S.7
Starkman, S.8
Orozco-Diaz, G.9
Lunkes, A.10
DeJong, P.11
Rouleau, G.A.12
Auburger, G.13
Korenberg, J.R.14
Figueroa, C.15
Sahba, S.16
-
28
-
-
0031025555
-
Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation and haplotype mapping of the SPG4 locus on the short arm of chromosome 2
-
Raskind WH, Pericak-Vance MA, Lennon F, Wolff J, Lipe HP, Bird TD (1997) Familial spastic paraparesis: evaluation of locus heterogeneity, anticipation and haplotype mapping of the SPG4 locus on the short arm of chromosome 2. Am J Med Genet 74:26-36
-
(1997)
Am J Med Genet
, vol.74
, pp. 26-36
-
-
Raskind, W.H.1
Pericak-Vance, M.A.2
Lennon, F.3
Wolff, J.4
Lipe, H.P.5
Bird, T.D.6
-
29
-
-
0030292368
-
Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT
-
Sanpei K, Takano H, Igarashi S, Sato T, Oyake M, Sasaki H, Wakisaka A, Tashiro K, Ishida Y, Ikeuchi T, Koide R, Saito M, Sato A, Tanaka T, Hanyu S, Takiyama Y, Nishizawa M, Shimizu N, Nomura Y, Segawa M, Iwabuchi K, Eguchi I, Tanaka H, Takahashi H, Tsuji S (1996) Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT. Nat Genet 14:277-284
-
(1996)
Nat Genet
, vol.14
, pp. 277-284
-
-
Sanpei, K.1
Takano, H.2
Igarashi, S.3
Sato, T.4
Oyake, M.5
Sasaki, H.6
Wakisaka, A.7
Tashiro, K.8
Ishida, Y.9
Ikeuchi, T.10
Koide, R.11
Saito, M.12
Sato, A.13
Tanaka, T.14
Hanyu, S.15
Takiyama, Y.16
Nishizawa, M.17
Shimizu, N.18
Nomura, Y.19
Segawa, M.20
Iwabuchi, K.21
Eguchi, I.22
Tanaka, H.23
Takahashi, H.24
Tsuji, S.25
more..
-
30
-
-
0027256423
-
Direct detection of novel expanded trinucleotide repeats in the human genome
-
Schalling M, Hudson TJ, Buetow KH, Housman DE (1993) Direct detection of novel expanded trinucleotide repeats in the human genome. Nat Genet 4:135-139
-
(1993)
Nat Genet
, vol.4
, pp. 135-139
-
-
Schalling, M.1
Hudson, T.J.2
Buetow, K.H.3
Housman, D.E.4
-
32
-
-
0023651133
-
A model for the separation of large DNA molecules by crossed field gel electrophoresis
-
Southern E, Anand R, Brown W, Fletcher D (1987) A model for the separation of large DNA molecules by crossed field gel electrophoresis. Nucleic Acids Res 15:5925-5943
-
(1987)
Nucleic Acids Res
, vol.15
, pp. 5925-5943
-
-
Southern, E.1
Anand, R.2
Brown, W.3
Fletcher, D.4
-
33
-
-
0032813945
-
Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA
-
Theuns J, Cruts M, Del-Favero J, Goossens D, Dauwerse H, Wehnert A, Dunnen JT den, Van Broeckhoven C (1999) Determination of the genomic organization of human presenilin 1 by fiber-FISH analysis and restriction mapping of cloned DNA. Mamm Genome 10:410-414
-
(1999)
Mamm Genome
, vol.10
, pp. 410-414
-
-
Theuns, J.1
Cruts, M.2
Del-Favero, J.3
Goossens, D.4
Dauwerse, H.5
Wehnert, A.6
Den Dunnen, J.T.7
Van Broeckhoven, C.8
-
34
-
-
0028972448
-
Polyglutamine expansions as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias
-
Trottier Y, Lutz Y, Stevanin G, Imbert G, Devys D, Cancel G, Saudou F, Weber C, David G, Tora L, Agid Y, Brice A, Mandel JL (1995) Polyglutamine expansions as a pathological epitope in Huntington's disease and four dominant cerebellar ataxias. Nature 378:403-406
-
(1995)
Nature
, vol.378
, pp. 403-406
-
-
Trottier, Y.1
Lutz, Y.2
Stevanin, G.3
Imbert, G.4
Devys, D.5
Cancel, G.6
Saudou, F.7
Weber, C.8
David, G.9
Tora, L.10
Agid, Y.11
Brice, A.12
Mandel, J.L.13
-
35
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJMH, Pieretti M, Sutcliffe JS, Fu Y-H, Kuhl DPA, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang F, Eussen BE, Ommen G-J van, Blonden L, Riggins GJ, Chastain JL, Kunst CB, Galjaard H, Caskey CT, Nelson DL, Oostra BA, Warren ST (1991) Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 65:905-914
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.-H.4
Kuhl, D.P.A.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
Eussen, B.E.11
Van Ommen, G.-J.12
Blonden, L.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
36
-
-
0031012399
-
1A-voltage-dependent calcium channel
-
1A-voltage-dependent calcium channel. Nat Genet 15:62-69
-
(1997)
Nat Genet
, vol.15
, pp. 62-69
-
-
Zhuchenko, O.1
Bailey, J.2
Bonnen, P.3
Ashizawa, T.4
Stockton, D.W.5
Amos, C.6
Dobyns, W.7
Subramony, S.H.8
Zoghbi, H.Y.9
Lee, C.C.10
|