-
1
-
-
0031909907
-
Why is the centromere so cold?
-
Choo, K.H.A. (1998) Why is the centromere so cold? Genome Res., 8, 81-82.
-
(1998)
Genome Res.
, vol.8
, pp. 81-82
-
-
Choo, K.H.A.1
-
2
-
-
0343182998
-
A 9.75-Mb map across the centromere of human chromosome 10
-
Jackson, M.S., Gee See, C., Mulligan, L.M. and Lauffart, B.F. (1996) A 9.75-Mb map across the centromere of human chromosome 10. Genomics, 33, 258-270.
-
(1996)
Genomics
, vol.33
, pp. 258-270
-
-
Jackson, M.S.1
Gee See, C.2
Mulligan, L.M.3
Lauffart, B.F.4
-
3
-
-
14444286943
-
X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content
-
Nagaraja, R., MacMillan, S., Kere, J., Jones, C., Griffin, S., Schmatz, M., Terrell, J., Shomaker, M., Jermak, C., Hott, C. et al. (1997) X chromosome map at 75-kb STS resolution, revealing extremes of recombination and GC content. Genome Res., 7, 210-222.
-
(1997)
Genome Res.
, vol.7
, pp. 210-222
-
-
Nagaraja, R.1
MacMillan, S.2
Kere, J.3
Jones, C.4
Griffin, S.5
Schmatz, M.6
Terrell, J.7
Shomaker, M.8
Jermak, C.9
Hott, C.10
-
4
-
-
0031911344
-
Physical and genetic mapping of the human X chromosome centromere: Repression of recombination
-
Mahtani, M.M. and Willard, H.F. (1998) Physical and genetic mapping of the human X chromosome centromere: repression of recombination. Genome Res., 8, 100-110.
-
(1998)
Genome Res.
, vol.8
, pp. 100-110
-
-
Mahtani, M.M.1
Willard, H.F.2
-
5
-
-
0033558974
-
Genetic and physical analyses of the pericentromeric regions of human chromosomes 5 and 19. Recombination across 5cen
-
Puechberty, J., Laurent, A.-M., Gimenez, S., Billault, A., Brun-Laurent, M.-E., Calenda, A., Marcais, B., Prades, C., Ioannou, P., Yurov, Y. et al. (1999) Genetic and physical analyses of the pericentromeric regions of human chromosomes 5 and 19. Recombination across 5cen. Genomics, 56, 274-287.
-
(1999)
Genomics
, vol.56
, pp. 274-287
-
-
Puechberty, J.1
Laurent, A.-M.2
Gimenez, S.3
Billault, A.4
Brun-Laurent, M.-E.5
Calenda, A.6
Marcais, B.7
Prades, C.8
Ioannou, P.9
Yurov, Y.10
-
6
-
-
0032518613
-
Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19
-
Mohrenweiser, H.W., Tsujimoto, S., Gordon, L. and Olsen, A.S. (1998) Regions of sex-specific hypo- and hyper-recombination identified through integration of 180 genetic markers into the metric physical map of human chromosome 19. Genomics, 47, 153-162.
-
(1998)
Genomics
, vol.47
, pp. 153-162
-
-
Mohrenweiser, H.W.1
Tsujimoto, S.2
Gordon, L.3
Olsen, A.S.4
-
7
-
-
0035475786
-
Lessons from the human genome: Transitions between euchromatin and heterochromatin
-
Horvath, J.E., Bailey, J.A., Locke, D.P. and Eichler, E.E. (2001) Lessons from the human genome: transitions between euchromatin and heterochromatin. Hum. Mol. Genet., 10, 2215-2223.
-
(2001)
Hum. Mol. Genet.
, vol.10
, pp. 2215-2223
-
-
Horvath, J.E.1
Bailey, J.A.2
Locke, D.P.3
Eichler, E.E.4
-
8
-
-
0034831138
-
Segmental duplications: Organization and impact within the current human genome project assembly
-
Bailey, J.A., Yavor, A.M., Massa, H.F., Trask, B.J. and Eichler, E.E. (2001) Segmental duplications: organization and impact within the current human genome project assembly. Genome Res., 11, 1005-1017.
-
(2001)
Genome Res.
, vol.11
, pp. 1005-1017
-
-
Bailey, J.A.1
Yavor, A.M.2
Massa, H.F.3
Trask, B.J.4
Eichler, E.E.5
-
9
-
-
0037047628
-
Recent segmental duplications in the human genome
-
Bailey, J.A., Gu, Z., Clark, R.A., Reinert, K., Samonte, R.V., Schwartz, S., Adams, M.D., Myers, E.W., Li, P.W. and Eichler, E.E. (2002) Recent segmental duplications in the human genome. Science, 297, 1003-1007.
-
(2002)
Science
, vol.297
, pp. 1003-1007
-
-
Bailey, J.A.1
Gu, Z.2
Clark, R.A.3
Reinert, K.4
Samonte, R.V.5
Schwartz, S.6
Adams, M.D.7
Myers, E.W.8
Li, P.W.9
Eichler, E.E.10
-
10
-
-
0032231877
-
Comprehensive human genetic maps: Individual and sex-specific variation in recombination
-
Broman, K.W., Murray, J.C., Sheffield, V.C., White, R.L. and Weber, J.L. (1998) Comprehensive human genetic maps: individual and sex-specific variation in recombination. Am. J. Hum. Genet., 63, 861-869.
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 861-869
-
-
Broman, K.W.1
Murray, J.C.2
Sheffield, V.C.3
White, R.L.4
Weber, J.L.5
-
11
-
-
0035865094
-
Comparison of human genetic and sequence-based physical maps
-
Yu, A., Zhao, C., Fan, Y., Jang, W., Mungall, A.J., Deloukas, P., Olsen, A., Doggett, N.A., Ghebranious, N., Broman, K.W. et al. (2001) Comparison of human genetic and sequence-based physical maps. Nature, 409, 951-953.
-
(2001)
Nature
, vol.409
, pp. 951-953
-
-
Yu, A.1
Zhao, C.2
Fan, Y.3
Jang, W.4
Mungall, A.J.5
Deloukas, P.6
Olsen, A.7
Doggett, N.A.8
Ghebranious, N.9
Broman, K.W.10
-
12
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong, A., Gudbjartsson, D.F., Sainz, J., Jonsdottir, G.M., Gudjonsson, S.A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G. et al. (2002) A high-resolution recombination map of the human genome. Nat. Genet., 31, 241-247.
-
(2002)
Nat. Genet.
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
-
13
-
-
0033804332
-
Patterns of meiotic recombination on the long arm of human chromosome 21
-
Lynn, A., Kashuk, C., Petersen, M.B., Bailey, J.A., Cox, DR., Antonarakis, S.E. and Chakravarti, A. (2000) Patterns of meiotic recombination on the long arm of human chromosome 21. Genome Res., 10, 1319-1332.
-
(2000)
Genome Res.
, vol.10
, pp. 1319-1332
-
-
Lynn, A.1
Kashuk, C.2
Petersen, M.B.3
Bailey, J.A.4
Cox, D.R.5
Antonarakis, S.E.6
Chakravarti, A.7
-
14
-
-
0027506362
-
A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13E
-
van Hul, W., van Camp, G., Stuyver, L., Delabar, J.M., McInnis, M.G., Warren, A.C., Antonarakis, S.E. and van Broeckhoven, C. (1993) A contiguous physical map of the pericentromeric region of chromosome 21q between D21Z1 and D21S13E. Genomics, 15, 626-630.
-
(1993)
Genomics
, vol.15
, pp. 626-630
-
-
van Hul, W.1
van Camp, G.2
Stuyver, L.3
Delabar, J.M.4
McInnis, M.G.5
Warren, A.C.6
Antonarakis, S.E.7
van Broeckhoven, C.8
-
15
-
-
0033753766
-
Counting cross-overs: Characterizing meiotic recombination in mammals
-
Hassold, T., Sherman, S. and Hunt, P. (2000) Counting cross-overs: characterizing meiotic recombination in mammals. Hum. Mol. Genet., 9, 2409-2419.
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 2409-2419
-
-
Hassold, T.1
Sherman, S.2
Hunt, P.3
-
16
-
-
0035319804
-
To err (meiotically) is human: The genesis of human aneuploidy
-
Hassold, T. and Hunt, P. (2001) To err (meiotically) is human: the genesis of human aneuploidy. Nat. Rev. Genet., 2, 280-291.
-
(2001)
Nat. Rev. Genet.
, vol.2
, pp. 280-291
-
-
Hassold, T.1
Hunt, P.2
-
17
-
-
9844220844
-
Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21
-
Lamb, N.E., Feingold, E., Savage, A., Avramopoulos, D., Freeman, S., Gu, Y., Hallberg, A., Hersey, J., Karadima, G., Pettay, D. et al. (1997) Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21. Hum. Mol. Genet., 6, 1391-1399.
-
(1997)
Hum. Mol. Genet.
, vol.6
, pp. 1391-1399
-
-
Lamb, N.E.1
Feingold, E.2
Savage, A.3
Avramopoulos, D.4
Freeman, S.5
Gu, Y.6
Hallberg, A.7
Hersey, J.8
Karadima, G.9
Pettay, D.10
-
18
-
-
10544226872
-
Susceptible chiasmate configurations of chromosome 21 predispose to nondisjunction in both maternal meiosis-I and meiosis-II
-
Lamb, N.E., Freeman, S.B., Savageaustin, A., Pettay, D., Taft, L., Hersey, J., Gu, Y.C., Shen, J., Saker, D., May, K.M. et al. (1996) Susceptible chiasmate configurations of chromosome 21 predispose to nondisjunction in both maternal meiosis-I and meiosis-II. Nat. Genet., 14, 400-405.
-
(1996)
Nat. Genet.
, vol.14
, pp. 400-405
-
-
Lamb, N.E.1
Freeman, S.B.2
Savageaustin, A.3
Pettay, D.4
Taft, L.5
Hersey, J.6
Gu, Y.C.7
Shen, J.8
Saker, D.9
May, K.M.10
-
19
-
-
0026536404
-
The meiotic stage of nondisjunction in trisomy 21: Determination by using DNA polymorphisms
-
Antonarakis, S.E., Petersen, M.B., McInnis, M.G., Adelsberger, P.A., Schinzel, A.A., Binkert, F., Pangalos, C., Raoul, O., Slaugenhaupt, S.A., Hafez, M. et al. (1992) The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms. Am. J. Hum. Genet., 50, 544-550.
-
(1992)
Am. J. Hum. Genet.
, vol.50
, pp. 544-550
-
-
Antonarakis, S.E.1
Petersen, M.B.2
McInnis, M.G.3
Adelsberger, P.A.4
Schinzel, A.A.5
Binkert, F.6
Pangalos, C.7
Raoul, O.8
Slaugenhaupt, S.A.9
Hafez, M.10
-
20
-
-
0031926521
-
Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome
-
Shen, J.J., Sherman, S.L. and Hassold, T.J. (1998) Centromeric genotyping and direct analysis of nondisjunction in humans: Down syndrome. Chromosoma, 107, 166-172.
-
(1998)
Chromosoma
, vol.107
, pp. 166-172
-
-
Shen, J.J.1
Sherman, S.L.2
Hassold, T.J.3
-
21
-
-
0024379003
-
Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: High-frequency array-length polymorphism and meiotic stability
-
Wevrick, R. and Willard, H.F. (1989) Long-range organization of tandem arrays of alpha satellite DNA at the centromeres of human chromosomes: high-frequency array-length polymorphism and meiotic stability. Proc. Natl Acad. Sci. USA, 86, 9394-9398.
-
(1989)
Proc. Natl Acad. Sci. USA
, vol.86
, pp. 9394-9398
-
-
Wevrick, R.1
Willard, H.F.2
-
22
-
-
0024989298
-
Pulse-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: High-frequency polymorphisms and array size estimate
-
Mahtani, M.M. and Willard, H.F. (1990) Pulse-field gel analysis of alpha-satellite DNA at the human X chromosome centromere: high-frequency polymorphisms and array size estimate. Genomics, 7, 607-613.
-
(1990)
Genomics
, vol.7
, pp. 607-613
-
-
Mahtani, M.M.1
Willard, H.F.2
-
23
-
-
0025963016
-
Structural organization and polymorphism of the alpha-satellite DNA sequences of chromosomes 13 and 21 as revealed by pulse field gel electrophoresis
-
Marcais, B., Bellis, M., Gerard, A., Pages, M., Boublik, Y. and Roizès, G. (1991) Structural organization and polymorphism of the alpha-satellite DNA sequences of chromosomes 13 and 21 as revealed by pulse field gel electrophoresis. Hum. Genet., 86, 311-316.
-
(1991)
Hum. Genet.
, vol.86
, pp. 311-316
-
-
Marcais, B.1
Bellis, M.2
Gerard, A.3
Pages, M.4
Boublik, Y.5
Roizès, G.6
-
24
-
-
0026032076
-
Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both
-
Jabs, E.W., Warren, A.C., Taylor, E.W., Colyer, C.R., Meyers, D.A. and Antonarakis, S.E. (1991) Alphoid DNA polymorphisms for chromosome 21 can be distinguished from those of chromosome 13 using probes homologous to both. Genomics, 9, 141-146.
-
(1991)
Genomics
, vol.9
, pp. 141-146
-
-
Jabs, E.W.1
Warren, A.C.2
Taylor, E.W.3
Colyer, C.R.4
Meyers, D.A.5
Antonarakis, S.E.6
-
25
-
-
0032717569
-
Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21
-
Lo, A.W., Liao, G.C., Rocchi, M. and Choo, K.H. (1999) Extreme reduction of chromosome-specific alpha-satellite array is unusually common in human chromosome 21. Genome Res., 9, 895-908.
-
(1999)
Genome Res.
, vol.9
, pp. 895-908
-
-
Lo, A.W.1
Liao, G.C.2
Rocchi, M.3
Choo, K.H.4
-
26
-
-
0034091399
-
Variation in alphoid DNA size and trisomy 21: A possible cause of nondisjunction
-
Maratou, K., Siddique, Y., Kessling, A.M. and Davies, G.E. (2000) Variation in alphoid DNA size and trisomy 21: a possible cause of nondisjunction. Hum. Genet., 106, 525-530.
-
(2000)
Hum. Genet.
, vol.106
, pp. 525-530
-
-
Maratou, K.1
Siddique, Y.2
Kessling, A.M.3
Davies, G.E.4
-
27
-
-
0002694406
-
Crossing over in heterochromatin
-
Baker, W.K. (1958) Crossing over in heterochromatin. Am. Nat., 92, 59-60.
-
(1958)
Am. Nat.
, vol.92
, pp. 59-60
-
-
Baker, W.K.1
-
28
-
-
0017811348
-
Genetic studies on heterochromatin in Drosophila melanogaster and their implications for the functions of satellite DNA
-
Yamamoto, M. and Miklos, G.L.G. (1978) Genetic studies on heterochromatin in Drosophila melanogaster and their implications for the functions of satellite DNA. Chromosoma, 66, 71-98.
-
(1978)
Chromosoma
, vol.66
, pp. 71-98
-
-
Yamamoto, M.1
Miklos, G.L.G.2
-
29
-
-
0034682403
-
The DNA sequence of human chromosome 21
-
Hattori, M., Fujiyama, A., Taylor, T.D., Watanabe, H., Yada, T., Park, H.S., Toyoda, A., Ishii, K., Totoki, Y., Choi, D.K. et al. (2000) The DNA sequence of human chromosome 21. Nature, 405, 311-319.
-
(2000)
Nature
, vol.405
, pp. 311-319
-
-
Hattori, M.1
Fujiyama, A.2
Taylor, T.D.3
Watanabe, H.4
Yada, T.5
Park, H.S.6
Toyoda, A.7
Ishii, K.8
Totoki, Y.9
Choi, D.K.10
-
30
-
-
0026768544
-
D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21
-
Warren, A.C., Petersen, M.B., van Hul, W., McInnis, M.G., van Broeckhoven, C., Cox, T.K., Chakravarti, A. and Antonarakis, S.E. (1992) D21S215 is a (GT)n polymorphic marker close to centromeric alphoid sequences on chromosome 21. Genomics, 13, 1365-1367.
-
(1992)
Genomics
, vol.13
, pp. 1365-1367
-
-
Warren, A.C.1
Petersen, M.B.2
van Hul, W.3
McInnis, M.G.4
van Broeckhoven, C.5
Cox, T.K.6
Chakravarti, A.7
Antonarakis, S.E.8
-
31
-
-
0027366508
-
Isolation and characterization of 14 CA-repeat microsatellites from human chromosome 21
-
Bosch, A., Nunes, V., Patterson, D. and Estivill, X. (1993) Isolation and characterization of 14 CA-repeat microsatellites from human chromosome 21. Genomics, 18, 151-155.
-
(1993)
Genomics
, vol.18
, pp. 151-155
-
-
Bosch, A.1
Nunes, V.2
Patterson, D.3
Estivill, X.4
-
32
-
-
0030801002
-
Gapped BLAST and PSI-BLAST: A new generation of protein database search programs
-
Altschul, S.F., Madden, T.L., Schaffer, A.A., Zhang, J., Zhang, Z., Miller, W. and Lipman, D.J. (1997) Gapped BLAST and PSI-BLAST: a new generation of protein database search programs. Nucl. Acids Res., 25, 3389-3402.
-
(1997)
Nucl. Acids Res.
, vol.25
, pp. 3389-3402
-
-
Altschul, S.F.1
Madden, T.L.2
Schaffer, A.A.3
Zhang, J.4
Zhang, Z.5
Miller, W.6
Lipman, D.J.7
-
33
-
-
0024605518
-
Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
-
Newton, C.R., Graham, A., Heptinstall, L.E., Powell, S.J., Summers, C., Kalsheker, N., Smith, J.C. and Markham, A.F. (1989) Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS). Nucl. Acids Res., 17, 2503-2516.
-
(1989)
Nucl. Acids Res.
, vol.17
, pp. 2503-2516
-
-
Newton, C.R.1
Graham, A.2
Heptinstall, L.E.3
Powell, S.J.4
Summers, C.5
Kalsheker, N.6
Smith, J.C.7
Markham, A.F.8
-
34
-
-
0033916868
-
The mosaic structure of human pericentromeric DNA: A strategy for characterizing complex regions of the human genome
-
Horvath, J.E., Schwartz, S. and Eichler, E.E. (2000) The mosaic structure of human pericentromeric DNA: a strategy for characterizing complex regions of the human genome. Genome Res., 10, 839-852.
-
(2000)
Genome Res.
, vol.10
, pp. 839-852
-
-
Horvath, J.E.1
Schwartz, S.2
Eichler, E.E.3
-
35
-
-
0029877887
-
The effect of y-chromosome alpha-satellite array length on the rate of sex-chromosome disomy in human sperm
-
Abruzzo, M.A., Griffin, D.K., Millie, E.A., Sheean, L.A. and Hassold, T.J. (1996) The effect of y-chromosome alpha-satellite array length on the rate of sex-chromosome disomy in human sperm. Hum. Genet., 97, 819-823.
-
(1996)
Hum. Genet.
, vol.97
, pp. 819-823
-
-
Abruzzo, M.A.1
Griffin, D.K.2
Millie, E.A.3
Sheean, L.A.4
Hassold, T.J.5
-
36
-
-
0026676193
-
Nondisjunction of chromosome 21: Comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin
-
Lorber, B.J., Grantham, M., Peters, J., Willard, H.F. and Hassold, T.J. (1992) Nondisjunction of chromosome 21: comparisons of cytogenetic and molecular studies of the meiotic stage and parent of origin. Am. J. Hum. Genet., 51, 1265-1276.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1265-1276
-
-
Lorber, B.J.1
Grantham, M.2
Peters, J.3
Willard, H.F.4
Hassold, T.J.5
-
37
-
-
0026785123
-
Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome
-
Petersen, M.B., Frantzen, M., Antonarakis, S.E., Warren, A.C., van Broeckhoven, C., Chakravarti, A., Cox, T.K., Lund, C., Olsen, B., Poulsen, H. et al. (1992) Comparative study of microsatellite and cytogenetic markers for detecting the origin of the nondisjoined chromosome 21 in Down syndrome. Am. J. Hum. Genet., 51, 516-525.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 516-525
-
-
Petersen, M.B.1
Frantzen, M.2
Antonarakis, S.E.3
Warren, A.C.4
van Broeckhoven, C.5
Chakravarti, A.6
Cox, T.K.7
Lund, C.8
Olsen, B.9
Poulsen, H.10
-
38
-
-
0037320553
-
Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction
-
Berend, S.A., Page, S.L., Atkinson, W., McCaskill, C., Lamb, N.E., Sherman, S.L. and Shaffer, L.G. (2003) Obligate short-arm exchange in de novo Robertsonian translocation formation influences placement of crossovers in chromosome 21 nondisjunction. Am. J. Hum. Genet., 72, 488-495.
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 488-495
-
-
Berend, S.A.1
Page, S.L.2
Atkinson, W.3
McCaskill, C.4
Lamb, N.E.5
Sherman, S.L.6
Shaffer, L.G.7
-
39
-
-
0035941029
-
Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21
-
Patil, N., Berno, A.J., Hinds, D.A., Barrett, W.A., Doshi, J.M., Hacker, C.R., Kautzer, C.R., Lee, D.H., Marjoribanks, C., McDonough, D.P. et al. (2001) Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. Science, 294, 1719-1723.
-
(2001)
Science
, vol.294
, pp. 1719-1723
-
-
Patil, N.1
Berno, A.J.2
Hinds, D.A.3
Barrett, W.A.4
Doshi, J.M.5
Hacker, C.R.6
Kautzer, C.R.7
Lee, D.H.8
Marjoribanks, C.9
McDonough, D.P.10
-
40
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
Sachidanandam, R., Weissman, D., Schmidt, S.C., Kakol, J.M., Stein, L.D., Marth, G., Sherry, S., Mullikin, J.C., Mortimore, B.J., Willey, D.L. et al. (2001) A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature, 409, 928-933.
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
Weissman, D.2
Schmidt, S.C.3
Kakol, J.M.4
Stein, L.D.5
Marth, G.6
Sherry, S.7
Mullikin, J.C.8
Mortimore, B.J.9
Willey, D.L.10
-
41
-
-
0027379760
-
Long-range analyses of the centromeric regions of human chromosomes 13, 14 and 21: Identification of a narrow domain containing two key centromeric DNA elements
-
Trowell, H.E., Nagy, A., Vissel, B. and Choo, K.H.A. (1993) Long-range analyses of the centromeric regions of human chromosomes 13, 14 and 21: identification of a narrow domain containing two key centromeric DNA elements. Hum. Mol. Genet., 2, 1639-1649.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1639-1649
-
-
Trowell, H.E.1
Nagy, A.2
Vissel, B.3
Choo, K.H.A.4
-
42
-
-
0033555906
-
Tandem repeats finder: A program to analyze DNA sequences
-
Benson, G. (1999) Tandem repeats finder: a program to analyze DNA sequences. Nucl. Acids Res., 27, 573-580.
-
(1999)
Nucl. Acids Res.
, vol.27
, pp. 573-580
-
-
Benson, G.1
-
43
-
-
0027968068
-
CLUSTAL W: Improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
-
Thompson, J.D., Higgins, D.G. and Gibson, T.J. (1994) CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice. Nucl. Acids Res., 22, 4673-4680.
-
(1994)
Nucl. Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
44
-
-
0025141652
-
Repeat unit sequence variation in minisatellites: A novel source of DNA polymorphism for studying variation and mutation by single molecule analysis
-
Jeffreys, A.J., Neumann, R. and Wilson, V. (1990) Repeat unit sequence variation in minisatellites: a novel source of DNA polymorphism for studying variation and mutation by single molecule analysis. Cell, 60, 473-485.
-
(1990)
Cell
, vol.60
, pp. 473-485
-
-
Jeffreys, A.J.1
Neumann, R.2
Wilson, V.3
|