-
1
-
-
0344713060
-
Unusual form of cerebellar ataxia: Combined dentatorubral and pallidoluysian degeneration
-
Smith, J.K., Gonda, V.E. and Malamud. N. (1958) Unusual form of cerebellar ataxia: combined dentatorubral and pallidoluysian degeneration. Neurology, 13, 266-269.
-
(1958)
Neurology
, vol.13
, pp. 266-269
-
-
Smith, J.K.1
Gonda, V.E.2
Malamud, N.3
-
2
-
-
0020064620
-
Familial myoclonus epilepsy and choreoathetosis: Hereditary dentatorubral-pallidoluysian atrophy
-
Naito, H. and Oyanagi, S. (1982) Familial myoclonus epilepsy and choreoathetosis: hereditary dentatorubral-pallidoluysian atrophy. Neurology, 32, 798-807.
-
(1982)
Neurology
, vol.32
, pp. 798-807
-
-
Naito, H.1
Oyanagi, S.2
-
3
-
-
0023680089
-
Hereditary dentatorubral-pallidoluysian atrophy: Clinical and pathologic variants in a family
-
Takahashi, H., Ohama, E., Naito, H., Takeda, S., Nakashima, S., Makifuchi, T. and Ikuta, F. (1988) Hereditary dentatorubral-pallidoluysian atrophy: clinical and pathologic variants in a family. Neurology, 38, 1065-1070.
-
(1988)
Neurology
, vol.38
, pp. 1065-1070
-
-
Takahashi, H.1
Ohama, E.2
Naito, H.3
Takeda, S.4
Nakashima, S.5
Makifuchi, T.6
Ikuta, F.7
-
4
-
-
0005228985
-
Progressive myoclonus epilepsies and DRPLA
-
Naito, H. (1990) Progressive myoclonus epilepsies and DRPLA [in Japanese with English abstract]. Shinnkei-Kenkyu no Shinpo, 34, 56-67.
-
(1990)
Shinnkei-Kenkyu no Shinpo
, vol.34
, pp. 56-67
-
-
Naito, H.1
-
5
-
-
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. and Tsuji, S. (1994) Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA). Nature Genet., 6, 9-13.
-
(1994)
Nature 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
-
6
-
-
0028335386
-
Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
-
Nagafuchi, S., Yanagisawa, H., Saito, K., Shirayama, T., Ohsaki, E., Bundo, M., Takeda, T., Tadokoro, K., Kondo, I., Murayama, N., Tanaka, Y., Kikushima, H., Umino, K., Kurosawa, H., Furukawa, T., Nihei, K., Inoue, T., Sana, A., Komure, O., Takahashi, M., Yoshizawa, T., Kanazawa, I. and Yamada, M. (1994) Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p. Nature Genet., 6, 14-18.
-
(1994)
Nature Genet.
, vol.6
, pp. 14-18
-
-
Nagafuchi, S.1
Yanagisawa, H.2
Saito, K.3
Shirayama, T.4
Ohsaki, E.5
Bundo, M.6
Takeda, T.7
Tadokoro, K.8
Kondo, I.9
Murayama, N.10
Tanaka, Y.11
Kikushima, H.12
Umino, K.13
Kurosawa, H.14
Furukawa, T.15
Nihei, K.16
Inoue, T.17
Sana, A.18
Komure, O.19
Takahashi, M.20
Yoshizawa, T.21
Kanazawa, I.22
Yamada, M.23
more..
-
7
-
-
0027164698
-
Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1
-
Orr, H.T., Chung, M., Banfi, S., Kwiatkowski, T.J. Jr. Servadio, A., Beaudet, A.L., McCall, A.E., Duvick, L.A., Ranum, L.P.W. and Zoghbi, H.Y. (1993) Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. Nature Genet., 4, 221-226.
-
(1993)
Nature Genet.
, vol.4
, pp. 221-226
-
-
Orr, H.T.1
Chung, M.2
Banfi, S.3
Kwiatkowski T.J., Jr.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
-
8
-
-
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, T., 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. and Tsuji, S. (1996) Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT. Nature Genet., 14, 277-284.
-
(1996)
Nature 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, T.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..
-
9
-
-
0030292488
-
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst, S.-M., Nechiporuk, A., Nechiporuk, T., Gispert, S., Chen, X.-N., Lopes-Cendes, I., Pearlman, S., Starkman, S., Orozco-Diaz, G., Lunkes, A., DeJong, P., Rouleau, G.A., Auburger, G., Korenberg, J.R., Figueroa, C. and Sahba, S. (1996) Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genet., 14, 269-276.
-
(1996)
Nature 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
-
10
-
-
0030294345
-
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats
-
Imbert, G., Saudou, F., Yvert, G., Devys, D., Trottier, Y., Gamier, J.-M., Weber, C., Mandel, J.-L.G., Cancel, G., Abbas, N., Dürr, A., Didierjean, O., Stevanin, G., Agid, Y. and Brice, A.G. (1996) Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeats. Nature Genet., 14, 285-291.
-
(1996)
Nature Genet.
, vol.14
, pp. 285-291
-
-
Imbert, G.1
Saudou, F.2
Yvert, G.3
Devys, D.4
Trottier, Y.5
Gamier, J.-M.6
Weber, C.7
Mandel, J.-L.G.8
Cancel, G.9
Abbas, N.10
Dürr, A.11
Didierjean, O.12
Stevanin, G.13
Agid, Y.14
Brice, A.G.15
-
11
-
-
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. and Kakizuka, A. (1994) CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1. Nature Genet., 8, 221-227.
-
(1994)
Nature Genet.
, vol.8
, pp. 221-227
-
-
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
Kakizuka, A.13
-
12
-
-
0031012399
-
Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α-1 A-voltage-dependent calcium channel
-
Zuchenko, O., Bailey, J., Bonnen, P., Ashizawa, T., Stockton, D.W., Amos, C., Dobyns, W.B., Subramony, S.H., Zoghbi, H.Y. and Lee, C.C. (1997) Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α-1 A-voltage-dependent calcium channel. Nature Genet., 15, 62-69.
-
(1997)
Nature Genet.
, vol.15
, pp. 62-69
-
-
Zuchenko, O.1
Bailey, J.2
Bonnen, P.3
Ashizawa, T.4
Stockton, D.W.5
Amos, C.6
Dobyns, W.B.7
Subramony, S.H.8
Zoghbi, H.Y.9
Lee, C.C.10
-
13
-
-
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, J.-L. and Brice, A. (1977) Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion. Nature Genet., 17, 65-70.
-
(1977)
Nature 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
-
14
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The Huntington 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
-
-
-
15
-
-
0025800526
-
Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy
-
La Spada, A.R., Wilson, E.M., Lubahn, D.B., Harding, A.E. and Fishbeck, K.H. (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
Fishbeck, K.H.5
-
16
-
-
0029174129
-
Dentatorubral-pallidoluysian atrophy (DRPLA): Molecular basis for wide clinical features of DRPLA
-
Ikeuchi, T., Koide R., Onodera, O., Tanaka, H., Oyake, M., Takano, H. and Tsuji, S. (1995) Dentatorubral-pallidoluysian atrophy (DRPLA): molecular basis for wide clinical features of DRPLA. Clin. Neurosci., 3, 23-27.
-
(1995)
Clin. Neurosci.
, vol.3
, pp. 23-27
-
-
Ikeuchi, T.1
Koide, R.2
Onodera, O.3
Tanaka, H.4
Oyake, M.5
Takano, H.6
Tsuji, S.7
-
17
-
-
0029009456
-
Evidence for inter-generational instability in the CAG repeat in the MJDI gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease
-
Takiyama, Y., Igarashi, S., Rogaeva, E.A., Endo, K., Rogaev, E.I., Tanaka, H., Sherrington, R., Sanpei, K., Liang, Y., Saito, M.,Tsuda, T., Takano, H., Ikeda, M., Lin, C., Chi, H., Kennedy, J.L., Lang, A.E., Wherrett, J.R., Segawa, M., Nomura, Y., Yuasa, T., Weissenbach, J., Yoshida, M., Nishizawa, M., Kidd, K.K., Tsuji, S. and St George-Hyslop, P.H. (1995) Evidence for inter-generational instability in the CAG repeat in the MJDI gene and for conserved haplotypes at flanking markers amongst Japanese and Caucasian subjects with Machado-Joseph disease. Hum. Mol. Genet., 4, 1137-1146.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1137-1146
-
-
Takiyama, Y.1
Igarashi, S.2
Rogaeva, E.A.3
Endo, K.4
Rogaev, E.I.5
Tanaka, H.6
Sherrington, R.7
Sanpei, K.8
Liang, Y.9
Saito, M.10
Tsuda, T.11
Takano, H.12
Ikeda, M.13
Lin, C.14
Chi, H.15
Kennedy, J.L.16
Lang, A.E.17
Wherrett, J.R.18
Segawa, M.19
Nomura, Y.20
Yuasa, T.21
Weissenbach, J.22
Yoshida, M.23
Nishizawa, M.24
Kidd, K.K.25
Tsuji, S.26
St George-Hyslop, P.H.27
more..
-
18
-
-
2442761245
-
Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJDI) is affected by the genotype of the normal chromosome: Implication for the molecular mechanisms of the instability of the CAG repeat
-
Igarashi, S., Takiyama, Y., Cancel, G., Rogaeva, E.A., Sasaki, H., Wakisaka, A., Zhou, Y.X., Takano, H., Endo, K., Sanpei, K., Oyake, M., Tanaka, H., Stevanin, G., Abbas, N., Dürr, A., Rogaev, E.I., Sherrington, R., Tsuda, T., Ikeda, M., Cassa, E., Nishizawa, M., Benomar, A., Julien, J., Weissenbach, J., Wang, G.X., Agid, Y. St George-Hyslop, P.H., Brice, A. and Tsuji, S. (1996) Intergenerational instability of the CAG repeat of the gene for Machado-Joseph disease (MJDI) is affected by the genotype of the normal chromosome: implication for the molecular mechanisms of the instability of the CAG repeat. Hum. Mol. Genet., 5, 923-932.
-
(1996)
Hum. Mol. Genet.
, vol.5
, pp. 923-932
-
-
Igarashi, S.1
Takiyama, Y.2
Cancel, G.3
Rogaeva, E.A.4
Sasaki, H.5
Wakisaka, A.6
Zhou, Y.X.7
Takano, H.8
Endo, K.9
Sanpei, K.10
Oyake, M.11
Tanaka, H.12
Stevanin, G.13
Abbas, N.14
Dürr, A.15
Rogaev, E.I.16
Sherrington, R.17
Tsuda, T.18
Ikeda, M.19
Cassa, E.20
Nishizawa, M.21
Benomar, A.22
Julien, J.23
Weissenbach, J.24
Wang, G.X.25
Agid, Y.26
St George-Hyslop, P.H.27
Brice, A.28
Tsuji, S.29
more..
-
19
-
-
0029865956
-
Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: The mutant allele is preferentially transmitted in male meiosis
-
Ikeuchi, T., Igarashi, S., Takiyama, Y., Onodera, O., Oyake, M., Takano, H., Koide, R., Tanaka, H. and Tsuji, S. (1996) Non-Mendelian transmission in dentatorubral-pallidoluysian atrophy and Machado-Joseph disease: the mutant allele is preferentially transmitted in male meiosis. Am. J. Hum. Genet., 58, 730-733.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 730-733
-
-
Ikeuchi, T.1
Igarashi, S.2
Takiyama, Y.3
Onodera, O.4
Oyake, M.5
Takano, H.6
Koide, R.7
Tanaka, H.8
Tsuji, S.9
-
20
-
-
8544224974
-
Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJDI): Evidence for non-Mendelian transmission of the MJDI gene and for the effect of the intragenic CGG/GGG polymorphism on the Intergenerational instability
-
Takiyama, Y. Sakoe, K., Soutome, M., Namekawa, M., Ogawa, T., Nakano, I., Igarashi, S., Oyake, M., Tanaka, H., Tsuji, S. and Nishizawa, M. (1997) Single sperm analysis of the CAG repeats in the gene for Machado-Joseph disease (MJDI): evidence for non-Mendelian transmission of the MJDI gene and for the effect of the intragenic CGG/GGG polymorphism on the Intergenerational instability. Hum. Mol. Genet., 6, 1063-1068.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1063-1068
-
-
Takiyama, Y.1
Sakoe, K.2
Soutome, M.3
Namekawa, M.4
Ogawa, T.5
Nakano, I.6
Igarashi, S.7
Oyake, M.8
Tanaka, H.9
Tsuji, S.10
Nishizawa, M.11
-
21
-
-
0029084074
-
Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: Quantification of the mutation frequency spectrum
-
Leeflang, E.P., Zhang, L., Tavare, S., Hubert, R., Srinidhi, J., MacDonald, M.E., Myers, R.H., de Yong, M., Wexler, N.S., Gusella, J.F. and Arnheim, N. (1995) Single sperm analysis of the trinucleotide repeats in the Huntington's disease gene: quantification of the mutation frequency spectrum. Hum. Mol. Genet., 4, 1519-1526.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1519-1526
-
-
Leeflang, E.P.1
Zhang, L.2
Tavare, S.3
Hubert, R.4
Srinidhi, J.5
MacDonald, M.E.6
Myers, R.H.7
De Yong, M.8
Wexler, N.S.9
Gusella, J.F.10
Arnheim, N.11
-
22
-
-
0029130324
-
N repeats in parent-offspring pairs with Huntington disease
-
N repeats in parent-offspring pairs with Huntington disease. Am. J. Hum. Genet., 57, 593-602.
-
(1995)
Am. J. Hum. Genet.
, vol.57
, pp. 593-602
-
-
Ranen, N.G.1
Stine, O.C.2
Abbott, M.H.3
Sherr, M.4
Codori, A.-M.5
Franz, M.L.6
Chao, N.I.7
Chung, A.S.8
Pleasant, N.9
Callahan, C.10
Kasch, L.M.11
Ghaffari, M.12
Chase, G.A.13
Kazazian, H.H.14
Brandt, J.15
Folstein, S.E.16
Ross, C.A.17
-
23
-
-
7144256250
-
Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability
-
La Spada, A.R., Peterson, K.R., Meadows, S.A., McClain, M.E., Jeng, G., Chmelar, R.S., Haugen, H.A., Chen, K., Singer, M.J., Moore, D., Trask, B.J., Fischbeck, K.H., Clegg, C.H. and McKnight, G.S. (1998) Androgen receptor YAC transgenic mice carrying CAG 45 alleles show trinucleotide repeat instability. Hum. Mol. Genet., 7, 959-967.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 959-967
-
-
La Spada, A.R.1
Peterson, K.R.2
Meadows, S.A.3
McClain, M.E.4
Jeng, G.5
Chmelar, R.S.6
Haugen, H.A.7
Chen, K.8
Singer, M.J.9
Moore, D.10
Trask, B.J.11
Fischbeck, K.H.12
Clegg, C.H.13
McKnight, G.S.14
-
24
-
-
0027495515
-
Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I
-
Chung, M.Y., Ranum, L.P., Duvick, L.A., Servadio, A., Zoghbi, H.Y and Orr, H.T. (1993) Evidence for a mechanism predisposing to intergenerational CAG repeat instability in spinocerebellar ataxia type I. Nature Genet., 5, 254-258.
-
(1993)
Nature Genet.
, vol.5
, pp. 254-258
-
-
Chung, M.Y.1
Ranum, L.P.2
Duvick, L.A.3
Servadio, A.4
Zoghbi, H.Y.5
Orr, H.T.6
-
25
-
-
0030292488
-
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2
-
Pulst, S.M., Nechiporuk, A., Nechiporuk, T. Gispert, S., Chen, X.N., Lopes Cendes, I., Pearlman, S., Starkman, S., Orozco Diaz, G., Lunkes, A., DeJong, P., Rouleau, G.A., Auburger, G., Korenberg, J.R., Figueroa, C. and Sahba, S. (1996) Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. Nature Genet., 14, 269-276.
-
(1996)
Nature 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
-
26
-
-
0028925739
-
CAG repeat length variation in sperm from a patient with Kennedy's disease
-
Zhang, L., Fischbeck, K.H. and Arnheim, N. (1995) CAG repeat length variation in sperm from a patient with Kennedy's disease. Hum. Mol. Genet., 4, 303-305.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 303-305
-
-
Zhang, L.1
Fischbeck, K.H.2
Arnheim, N.3
-
27
-
-
0004136246
-
-
Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY
-
Maniatis, T., Fritsch, E.F. and Sambrook, J. (1989) Molecular Cloning: A Laboratory Manual, 2nd edn. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Edn.
-
-
Maniatis, T.1
Fritsch, E.F.2
Sambrook, J.3
-
28
-
-
0028364565
-
Complex gene conversion events in germline mutation at human minisatellites
-
Jeffreys, A.J., Tamaki, K., MacLeod, A., Monckton, D.G., Neil, D.L. and Armour, J.A.L. (1994) Complex gene conversion events in germline mutation at human minisatellites. Nature Genet., 6, 136-145.
-
(1994)
Nature Genet.
, vol.6
, pp. 136-145
-
-
Jeffreys, A.J.1
Tamaki, K.2
MacLeod, A.3
Monckton, D.G.4
Neil, D.L.5
Armour, J.A.L.6
-
29
-
-
0003505215
-
-
Academic Press, NY
-
Innis, M.A., Gelfand, D.H., Sninsky, J.J. and White, T.J. (1990) PCR Protocols: A Guide to Methods and Applications. Academic Press, NY.
-
(1990)
PCR Protocols: A Guide to Methods and Applications
-
-
Innis, M.A.1
Gelfand, D.H.2
Sninsky, J.J.3
White, T.J.4
-
30
-
-
0024399081
-
Single-sperm typing: Determination of genetic distance between the Gγ-globin and parathyroid hormone loci by using the polymerase chain reaction and allelc-specific oligomers
-
Cui, X., Li, H., Goradia, T.M., Lange, K., Kazazian, J.H.H., Galas, D. and Arnheim, N. (1989) Single-sperm typing: determination of genetic distance between the Gγ-globin and parathyroid hormone loci by using the polymerase chain reaction and allelc-specific oligomers. Proc. Natl Acad. Sci USA, 86, 9389-9393.
-
(1989)
Proc. Natl Acad. Sci USA
, vol.86
, pp. 9389-9393
-
-
Cui, X.1
Li, H.2
Goradia, T.M.3
Lange, K.4
Kazazian, J.H.H.5
Galas, D.6
Arnheim, N.7
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