-
1
-
-
0026518648
-
Survey of human and rat microsatellites
-
Beckmann, J. S., and Weber, J. L. (1992). Survey of human and rat microsatellites. Genomics 12: 627-631.
-
(1992)
Genomics
, vol.12
, pp. 627-631
-
-
Beckmann, J.S.1
Weber, J.L.2
-
2
-
-
0028814128
-
Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers
-
Bell, C. J., Nieuwenhuijsen, B. W., Barnoski, B., Budarf, M. L., Buetow, K. H., Campbell, K., Colbert, A., Collins, J., Desjardins, P. R., DeZwaan, T., Eckman, B., Fischbeck, K., Foote, S., Hart, K., Hiester, K., Van Het Hoog, M. J., Hopper, E., McDermid, H. E., Overton, C., Reeve, M. P., Searls, D. B., Watson, E., Winston, R., Valmiki, V. H., Nussbaum, R. L., Lander, E. S., Emanuel, B. S., and Hudson, T. J. (1995). Integration of physical, breakpoint and genetic maps of chromosome 22. Localization of 587 yeast artificial chromosomes with 238 mapped markers. Hum. Mol. Genet. 4: 59-69.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 59-69
-
-
Bell, C.J.1
Nieuwenhuijsen, B.W.2
Barnoski, B.3
Budarf, M.L.4
Buetow, K.H.5
Campbell, K.6
Colbert, A.7
Collins, J.8
Desjardins, P.R.9
DeZwaan, T.10
Eckman, B.11
Fischbeck, K.12
Foote, S.13
Hart, K.14
Hiester, K.15
Van Het Hoog, M.J.16
Hopper, E.17
McDermid, H.E.18
Overton, C.19
Reeve, M.P.20
Searls, D.B.21
Watson, E.22
Winston, R.23
Valmiki, V.H.24
Nussbaum, R.L.25
Lander, E.S.26
Emanuel, B.S.27
Hudson, T.J.28
more..
-
3
-
-
0026566108
-
Molecular basis of myotonic dystropy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member
-
Brook, J. D., McCurrach, M. E., Harley, H. G., Buckler, A. J., Church, D., Aburatani, H., Hunter, K., Stanton, V. P., Thirion, J.-P., Hudson, T., Sohn, R., Zemelman, B., Snell, R. G., Rundle, S. A., Crow, S., Davies, J., Shelbourne, P., Buxton, J., Jones, C., Juvonen, V., Johnson, K., Harper, P. S., Shaw, D. J., and Housman, D. E. (1992). Molecular basis of myotonic dystropy: Expansion of a trinucleotide (CTG) repeat at the 3′ end of a transcript encoding a protein kinase family member. Cell 68: 799-808.
-
(1992)
Cell
, vol.68
, pp. 799-808
-
-
Brook, J.D.1
McCurrach, M.E.2
Harley, H.G.3
Buckler, A.J.4
Church, D.5
Aburatani, H.6
Hunter, K.7
Stanton, V.P.8
Thirion, J.-P.9
Hudson, T.10
Sohn, R.11
Zemelman, B.12
Snell, R.G.13
Rundle, S.A.14
Crow, S.15
Davies, J.16
Shelbourne, P.17
Buxton, J.18
Jones, C.19
Juvonen, V.20
Johnson, K.21
Harper, P.S.22
Shaw, D.J.23
Housman, D.E.24
more..
-
4
-
-
0028169738
-
The Haw River syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African-American family
-
Burke, J. R., Wingfield, M. S., Lewis, K. E., Roses, A. D., Lee, J. E., Hulette, C., Pericak-Vance, M. A., and Vance, J. M. (1994). The Haw River Syndrome: Dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nature Genet. 7: 521-524.
-
(1994)
Nature Genet.
, vol.7
, pp. 521-524
-
-
Burke, J.R.1
Wingfield, M.S.2
Lewis, K.E.3
Roses, A.D.4
Lee, J.E.5
Hulette, C.6
Pericak-Vance, M.A.7
Vance, J.M.8
-
5
-
-
0001282761
-
Information enhancement methods for large scale sequence analysis
-
Claverie, J.-M., and States, D. J. (1993). Information enhancement methods for large scale sequence analysis. Comput. Chem. 17: 191-201.
-
(1993)
Comput. Chem.
, vol.17
, pp. 191-201
-
-
Claverie, J.-M.1
States, D.J.2
-
6
-
-
0026598119
-
An unstable triplet repeat in a gene related to myotonic muscular dystrophy
-
Fu, Y.-H., Pizzuti, A., Fenwick, R. G., Jr., King, J., Rajnarayan, S., Dunne, P. W., Dubel, J., Nasser, G. A., Ashizawa, T., De Jong, P., Wieringa, B., Korneluk, R., Perryman, M. B., Epstein, H. F., and Caskey, C. T. (1992). An unstable triplet repeat in a gene related to myotonic muscular dystrophy. Science 255: 1256-1258.
-
(1992)
Science
, vol.255
, pp. 1256-1258
-
-
Fu, Y.-H.1
Pizzuti, A.2
Fenwick R.G., Jr.3
King, J.4
Rajnarayan, S.5
Dunne, P.W.6
Dubel, J.7
Nasser, G.A.8
Ashizawa, T.9
De Jong, P.10
Wieringa, B.11
Korneluk, R.12
Perryman, M.B.13
Epstein, H.F.14
Caskey, C.T.15
-
7
-
-
0028885533
-
Survey of trinucleotide repeats in the human genome: Assessment of their utility as genetic markers
-
Gastier, J. M., Pulido, J. C., Sunden, S., Brody, T., Buetow, K. H., Murray, J. C., Weber, J. L., Hudson, T. J., Sheffield, V. C., and Duyk, G. M. (1995). Survey of trinucleotide repeats in the human genome: Assessment of their utility as genetic markers. Hum. Mol. Genet. 4: 1829-1836.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1829-1836
-
-
Gastier, J.M.1
Pulido, J.C.2
Sunden, S.3
Brody, T.4
Buetow, K.H.5
Murray, J.C.6
Weber, J.L.7
Hudson, T.J.8
Sheffield, V.C.9
Duyk, G.M.10
-
8
-
-
0027251874
-
Origin of the expansion mutation in myotonic dystrophy
-
Imbert, G., Kretz, C., Johnson, K., and Mandel, J.-L. (1993). Origin of the expansion mutation in myotonic dystrophy. Nature Genet. 4: 72-76.
-
(1993)
Nature Genet.
, vol.4
, pp. 72-76
-
-
Imbert, G.1
Kretz, C.2
Johnson, K.3
Mandel, J.-L.4
-
9
-
-
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
-
10
-
-
0027203684
-
Trinucleotide repeat amplification and hypermethylation of a Cpg island in FRAXE mental retardation
-
Knight, S. J. L., Flannery, A. V., Hirst, M. C., Campbell, L., Christodoulou, Z., Phelps, S. R., Pointon, J., Middleton-Price, H. R., Barnicoat, A., Pembrey, M. E., Holland, J., Oostra, B. A., Bobrow, M., and Davies, K. E. (1993). Trinucleotide repeat amplification and hypermethylation of a CpG island in FRAXE mental retardation. Cell 74: 127-134.
-
(1993)
Cell
, vol.74
, pp. 127-134
-
-
Knight, S.J.L.1
Flannery, A.V.2
Hirst, M.C.3
Campbell, L.4
Christodoulou, Z.5
Phelps, S.R.6
Pointon, J.7
Middleton-Price, H.R.8
Barnicoat, A.9
Pembrey, M.E.10
Holland, J.11
Oostra, B.A.12
Bobrow, M.13
Davies, K.E.14
-
11
-
-
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 Tsuiji, 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
Tsuiji, S.16
-
12
-
-
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 Fischbeck, 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
Fischbeck, K.H.5
-
13
-
-
0027297703
-
Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms
-
Li, S.-H., McInnis, M. G., Margolis, R. L., Antonarakis, S. E., and Ross, C. A. (1993). Novel triplet repeat containing genes in human brain: Cloning, expression, and length polymorphisms. Genomics 16: 572-579.
-
(1993)
Genomics
, vol.16
, pp. 572-579
-
-
Li, S.-H.1
McInnis, M.G.2
Margolis, R.L.3
Antonarakis, S.E.4
Ross, C.A.5
-
14
-
-
0029240699
-
Detection of expanded CAG repeats in bipolar affective disorder using the repeat expansion detection (RED) method
-
Linblad, K., Nylander, P.-O., De Bruyn, A., Sourey, D., Zander, C., Engstrom, C., Holmgren, G., Hudson, T., Chotai, J., Mendlewicz, J., Van Broeckhoven, C., Schalling, M., and Adolfsson, R. (1995). Detection of expanded CAG repeats in Bipolar Affective Disorder using the repeat expansion detection (RED) method. Neurobiol. Disease 2: 55-62.
-
(1995)
Neurobiol. Disease
, vol.2
, pp. 55-62
-
-
Linblad, K.1
Nylander, P.-O.2
De Bruyn, A.3
Sourey, D.4
Zander, C.5
Engstrom, C.6
Holmgren, G.7
Hudson, T.8
Chotai, J.9
Mendlewicz, J.10
Van Broeckhoven, C.11
Schalling, M.12
Adolfsson, R.13
-
15
-
-
23444459565
-
Growing triplet repeats
-
Linblad, K., Zander, C., Schalling, M., and Hudson, T. (1994). Growing triplet repeats. Nature Genet. 7: 124.
-
(1994)
Nature Genet.
, vol.7
, pp. 124
-
-
Linblad, K.1
Zander, C.2
Schalling, M.3
Hudson, T.4
-
16
-
-
0026603841
-
Myotonic dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene
-
Mahadevan, M., Tsilfidis, C., Sabourin, L., Shutler, G., Amemiya, C., Jansen, G., Neville, C., Narang, M., Barcelo, J., O'Hoy, K., Leblond, S., Earle-MacDonald, J., De Jong, P. J., Wieringa, B., and Korneluk, R. G. (1992). Myotonic Dystrophy mutation: An unstable CTG repeat in the 3′ untranslated region of the gene. Science 255: 1253-1255.
-
(1992)
Science
, vol.255
, pp. 1253-1255
-
-
Mahadevan, M.1
Tsilfidis, C.2
Sabourin, L.3
Shutler, G.4
Amemiya, C.5
Jansen, G.6
Neville, C.7
Narang, M.8
Barcelo, J.9
O'Hoy, K.10
Leblond, S.11
Earle-MacDonald, J.12
De Jong, P.J.13
Wieringa, B.14
Korneluk, R.G.15
-
17
-
-
0029066689
-
Inactivation of the type II TGF-β receptor in colon cancer cells with microsatellite instability
-
Markowitz, S., Wang, J., Myeroff, L., Parsons, R., Sun, L., Lutterbaugh, J., Fan, R. S., Zborowska, E., Kinzler, K. W., Vogelstein, B., Brattain, M., and Willson, J. K. V. (1995). Inactivation of the Type II TGF-β receptor in colon cancer cells with microsatellite instability. Science 268: 1336-1338.
-
(1995)
Science
, vol.268
, pp. 1336-1338
-
-
Markowitz, S.1
Wang, J.2
Myeroff, L.3
Parsons, R.4
Sun, L.5
Lutterbaugh, J.6
Fan, R.S.7
Zborowska, E.8
Kinzler, K.W.9
Vogelstein, B.10
Brattain, M.11
Willson, J.K.V.12
-
18
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density
-
Murray, J. C., Buetow, K. H., Weber, J. L., Ludwigsen, S., Scherpbier-Heddema, T., Manion, F., Quillen, J., Sheffield, V. C., Sunden, S., Duyk, G., Weissenbach, J., Gyapay, G., Dib, C., Morissette, J., Lathrop, G. M., Vignal, A., White, R., Matsunami, N., Gerken, S., Melis, R., Albertsen, H., Plaetke, R., Odelberg, S., Ward, D., Dausset, J., Cohen, D., and Cann, H. (1994). A comprehensive human linkage map with centimorgan density. Science 265: 2049-2054.
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
Manion, F.6
Quillen, J.7
Sheffield, V.C.8
Sunden, S.9
Duyk, G.10
Weissenbach, J.11
Gyapay, G.12
Dib, C.13
Morissette, J.14
Lathrop, G.M.15
Vignal, A.16
White, R.17
Matsunami, N.18
Gerken, S.19
Melis, R.20
Albertsen, H.21
Plaetke, R.22
Odelberg, S.23
Ward, D.24
Dausset, J.25
Cohen, D.26
Cann, H.27
more..
-
19
-
-
0028335386
-
Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p
-
Nagafuchi, S., Yanagisawa, H., Sato, 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., Sano, 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
Sato, 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
Sano, A.18
Komure, O.19
Takahashi, M.20
Yoshizawa, T.21
Kanazawa, I.22
Yamada, M.23
more..
-
20
-
-
0027981933
-
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
-
Nancarrow, J. K., Kremer, E., Holman, K., Eyre, H., Doggett, N. A., Le Paslier, D., Callen, D. F., Sutherland, G. R., and Richards, R. I. (1994). Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis. Science 264: 1938-1941.
-
(1994)
Science
, vol.264
, pp. 1938-1941
-
-
Nancarrow, J.K.1
Kremer, E.2
Holman, K.3
Eyre, H.4
Doggett, N.A.5
Le Paslier, D.6
Callen, D.F.7
Sutherland, G.R.8
Richards, R.I.9
-
21
-
-
0029355769
-
Expanded CAG repeats in schizophrenia and bipolar disorder
-
O'Donovan, M. C., Guy, C., Craddock, N., Murphy, K. C., Cardno, A. G., Jones, L. A., Owen, M. J., and McGufin, P. (1995). Expanded CAG repeats in schizophrenia and bipolar disorder. Nature Genet. 10: 380-381.
-
(1995)
Nature Genet.
, vol.10
, pp. 380-381
-
-
O'Donovan, M.C.1
Guy, C.2
Craddock, N.3
Murphy, K.C.4
Cardno, A.G.5
Jones, L.A.6
Owen, M.J.7
McGufin, P.8
-
22
-
-
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.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
-
23
-
-
0028099702
-
Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE
-
Parrish, J. E., Oostra, B. A., Verkerk, A. J. M. H., Richards, C. S., Reynolds, J., Spikes, A. S., Shaffer, L. G., and Nelson, D. L. (1994). Isolation of a GCC repeat showing expansion in FRAXF, a fragile site distal to FRAXA and FRAXE. Nature Genet. 8: 229-235.
-
(1994)
Nature Genet.
, vol.8
, pp. 229-235
-
-
Parrish, J.E.1
Oostra, B.A.2
Verkerk, A.J.M.H.3
Richards, C.S.4
Reynolds, J.5
Spikes, A.S.6
Shaffer, L.G.7
Nelson, D.L.8
-
24
-
-
0003203082
-
-
(N. C. Dracopoli, J. L. Haines, B. R. Korf, D. T. Moir, C. C. Morton, C. E. Seidman, J. G. Seidman, and D. R. Smith, Eds.), Wiley, New York
-
Pulido, J. C., and Duyk, G. M. (1994). In "Current Protocols in Human Genetics" (N. C. Dracopoli, J. L. Haines, B. R. Korf, D. T. Moir, C. C. Morton, C. E. Seidman, J. G. Seidman, and D. R. Smith, Eds.), Vol. 1, pp. 2.2.1-2.2.33, Wiley, New York.
-
(1994)
Current Protocols in Human Genetics
, vol.1
, pp. 221-2233
-
-
Pulido, J.C.1
Duyk, G.M.2
-
25
-
-
84970050019
-
Human genes containing polymorphic trinucleotide repeats
-
Riggins, G. J., Lokey, L. K., Chastain, J. L., Leiner, H. A., Sherman, S. L., Wilkinson, K. D., and Warren, S. T. (1992). Human genes containing polymorphic trinucleotide repeats. Nature Genet. 2: 186-191.
-
(1992)
Nature Genet.
, vol.2
, pp. 186-191
-
-
Riggins, G.J.1
Lokey, L.K.2
Chastain, J.L.3
Leiner, H.A.4
Sherman, S.L.5
Wilkinson, K.D.6
Warren, S.T.7
-
26
-
-
0027256423
-
Direct detection of novel expanded trinucleotide repeats in the human genome
-
Schalling, M., Hudson, T. J., Buetow, K. H., and Housman, D. E. (1993). Direct detection of novel expanded trinucleotide repeats in the human genome. Nature Genet. 4: 135-139.
-
(1993)
Nature Genet.
, vol.4
, pp. 135-139
-
-
Schalling, M.1
Hudson, T.J.2
Buetow, K.H.3
Housman, D.E.4
-
27
-
-
0041982299
-
Sequence similarity searching using the BLAST family of programs
-
(N. C. Dracopoli, J. L. Haines, B. R. Korf, D. T. Moir, C. C. Morton, C. E. Seidman, J. G. Seidman, and D. R. Smith, Eds.), Wiley, New York
-
Schuler, G. D., Boguski, M. S., and Gish, W. (1995). Sequence similarity searching using the BLAST family of programs. In "Current Protocols in Human Genetics" (N. C. Dracopoli, J. L. Haines, B. R. Korf, D. T. Moir, C. C. Morton, C. E. Seidman, J. G. Seidman, and D. R. Smith, Eds.), Vol. 12, pp. 11.3.1-11.3.37, Wiley, New York.
-
(1995)
Current Protocols in Human Genetics
, vol.12
, pp. 1131-11337
-
-
Schuler, G.D.1
Boguski, M.S.2
Gish, W.3
-
28
-
-
0028176566
-
Distribution of trinucleotide microsatellites in different categories of mammalian genomic sequences: Implications for human genetic diseases
-
Stallings, R. L. (1994). Distribution of trinucleotide microsatellites in different categories of mammalian genomic sequences: Implications for human genetic diseases. Genomics 21: 116-121.
-
(1994)
Genomics
, vol.21
, pp. 116-121
-
-
Stallings, R.L.1
-
29
-
-
0027480960
-
A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes
-
The 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
-
-
-
30
-
-
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, A. J. M. H., Pieretti, M., Sutcliffe, J. S., Fu, Y. H., Kuhl, D. P., Pizzuti, A., Reiner, O., Richards, S., Victoria, M. F., Zhang, F., Eussen, B. E., van Ommen, G.-J. B., Blonden, L. A. J., Riggins, G. J., Chastain, J. L., Kunst, C. B., Galjaard, H., Caskey, C. T., Nelson, D. L., Oostra, B. A., and Warren, S. T. (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.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.B.12
Blonden, L.A.J.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..
-
31
-
-
0026446099
-
A second-generation linkage map of the human genome
-
Weissenbach, J., Gyapay, G., Dib, C., Vignal, A., Morissette, J., Millasseau, P., Vaysseix, G., and Lathrop, M. (1992). A second-generation linkage map of the human genome. Nature 359: 794-801.
-
(1992)
Nature
, vol.359
, pp. 794-801
-
-
Weissenbach, J.1
Gyapay, G.2
Dib, C.3
Vignal, A.4
Morissette, J.5
Millasseau, P.6
Vaysseix, G.7
Lathrop, M.8
-
32
-
-
85029984259
-
Analysis of compositionally biased regions in sequence databases
-
in press
-
Wootton, J. C., and Federhen, S. Analysis of compositionally biased regions in sequence databases. Methods Enzymol., in press.
-
Methods Enzymol.
-
-
Wootton, J.C.1
Federhen, S.2
|