-
1
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S.F., Gish, W., Miller, W., Myers, E.W., and Lipman, D.J. 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
-
-
0041878461
-
Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements
-
Armengol, L., Pujana, M.A., Cheung, J., Scherer, S.W., and Estivill, X. 2003. Enrichment of segmental duplications in regions of breaks of synteny between the human and mouse genomes suggest their involvement in evolutionary rearrangements. Hum. Mol. Genet. 12: 2201-2208.
-
(2003)
Hum. Mol. Genet.
, vol.12
, pp. 2201-2208
-
-
Armengol, L.1
Pujana, M.A.2
Cheung, J.3
Scherer, S.W.4
Estivill, X.5
-
3
-
-
0347382445
-
Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution
-
Babcock, M., Pavlicek, A., Spiteri, E., Kashork, C.D., Ioshikhes, I., Shaffer, L.G., Jurka, J., and Morrow, B.E. 2003. Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution. Genome Res. 13: 2519-2532.
-
(2003)
Genome Res.
, vol.13
, pp. 2519-2532
-
-
Babcock, M.1
Pavlicek, A.2
Spiteri, E.3
Kashork, C.D.4
Ioshikhes, I.5
Shaffer, L.G.6
Jurka, J.7
Morrow, B.E.8
-
4
-
-
0142059650
-
An Alu transposition model for the origin and expansion of human segmental duplications
-
Bailey, J.A., Liu, G., and Eichler, E.E. 2003. An Alu transposition model for the origin and expansion of human segmental duplications. Am. J. Hum. Genet. 73: 823-834.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 823-834
-
-
Bailey, J.A.1
Liu, G.2
Eichler, E.E.3
-
5
-
-
0036250811
-
Alu repeats and human genomic diversity
-
Batzer, M.A. and Deininger, P.L. 2002. Alu repeats and human genomic diversity. Nat. Rev. Genet. 3: 370-379.
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 370-379
-
-
Batzer, M.A.1
Deininger, P.L.2
-
6
-
-
0038728033
-
Mutational mechanisms of Williams-Beuren syndrome deletions
-
Bayés, M., Magano, L.F., Rivera, N., Flores, R., and Pérez Jurado, L.A. 2003. Mutational mechanisms of Williams-Beuren syndrome deletions. Am. J. Hum. Genet. 73: 131-151.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 131-151
-
-
Bayés, M.1
Magano, L.F.2
Rivera, N.3
Flores, R.4
Pérez Jurado, L.A.5
-
7
-
-
1842667852
-
MAVID: Constrained ancestral alignment of multiple sequences
-
Bray, N. and Pachter, L. 2004. MAVID: Constrained ancestral alignment of multiple sequences. Genome Res. 14: 693-699.
-
(2004)
Genome Res.
, vol.14
, pp. 693-699
-
-
Bray, N.1
Pachter, L.2
-
8
-
-
0035130163
-
Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees
-
Chen, F.C. and Li, W.H. 2001. Genomic divergences between humans and other hominoids and the effective population size of the common ancestor of humans and chimpanzees. Am. J. Hum. Genet.68: 444-456
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 444-456
-
-
Chen, F.C.1
Li, W.H.2
-
9
-
-
0032971379
-
Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13)
-
Christian, S.L., Fantes, J.A., Mewborn, S.K., Huang, B., and Ledbetter, D.H. 1999. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11-q13). Hum. Mol. Genet. 8: 1025-1037.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1025-1037
-
-
Christian, S.L.1
Fantes, J.A.2
Mewborn, S.K.3
Huang, B.4
Ledbetter, D.H.5
-
10
-
-
0033036631
-
Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome
-
DeSilva, U., Massa, H., Trask, B.J., and Green, E.D. 1999. Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome. Genome Res. 9: 428-436.
-
(1999)
Genome Res.
, vol.9
, pp. 428-436
-
-
DeSilva, U.1
Massa, H.2
Trask, B.J.3
Green, E.D.4
-
11
-
-
0035500899
-
Recent duplication, domain accretion and the dynamic mutation of the human genome
-
Eichler, E.E. 2001. Recent duplication, domain accretion and the dynamic mutation of the human genome. Trends Genet. 17: 661-669.
-
(2001)
Trends Genet.
, vol.17
, pp. 661-669
-
-
Eichler, E.E.1
-
12
-
-
0032837598
-
Williams-Beuren syndrome: Genes and mechanisms
-
Francke, U. 1999. Williams-Beuren syndrome: Genes and mechanisms. Hum. Mol. Genet. 8: 1947-1954.
-
(1999)
Hum. Mol. Genet.
, vol.8
, pp. 1947-1954
-
-
Francke, U.1
-
13
-
-
0037351279
-
Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates
-
Frazer, K.A., Chen, X., Hinds, D.A., Pant, P.V., Patil, N., and Cox, D.R. 2003. Genomic DNA insertions and deletions occur frequently between humans and nonhuman primates. Genome Res. 13: 341-346.
-
(2003)
Genome Res.
, vol.13
, pp. 341-346
-
-
Frazer, K.A.1
Chen, X.2
Hinds, D.A.3
Pant, P.V.4
Patil, N.5
Cox, D.R.6
-
14
-
-
0032088632
-
Toward a phylogenetic classification of Primates based on DNA evidence complemented by fossil evidence
-
Goodman, M., Porter, C.A., Czelusniak, J., Page, S.L., Schneider, H., Shoshani, J., Gunnell, G., and Groves, C.P. 1998. Toward a phylogenetic classification of Primates based on DNA evidence complemented by fossil evidence. Mol. Phylogenet. Evol. 9: 585-598.
-
(1998)
Mol. Phylogenet. Evol.
, vol.9
, pp. 585-598
-
-
Goodman, M.1
Porter, C.A.2
Czelusniak, J.3
Page, S.L.4
Schneider, H.5
Shoshani, J.6
Gunnell, G.7
Groves, C.P.8
-
15
-
-
0040945789
-
A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease
-
Gorlach, A., Lee, P.L., Roesler, J., Hopkins, P.J., Christensen, B., Green, E.D., Chanock, S.J., and Curnutte, J.T. 1997. A p47-phox pseudogene carries the most common mutation causing p47-phox- deficient chronic granulomatous disease. J. Clin. Invest. 100: 1907-1918.
-
(1997)
J. Clin. Invest.
, vol.100
, pp. 1907-1918
-
-
Gorlach, A.1
Lee, P.L.2
Roesler, J.3
Hopkins, P.J.4
Christensen, B.5
Green, E.D.6
Chanock, S.J.7
Curnutte, J.T.8
-
16
-
-
0003706632
-
Gene duplication, exon shuffling and concerted evolution
-
(eds. D. Graur and W.H. Li). Sinauer Associates, Sunderland, MA
-
Graur, D. and Li, W-H. 2000. Gene duplication, exon shuffling and concerted evolution. In Fundamentals of molecular evolution, 2nd ed., (eds. D. Graur and W.H. Li). Sinauer Associates, Sunderland, MA.
-
(2000)
Fundamentals of Molecular Evolution, 2nd Ed.
-
-
Graur, D.1
Li, W.-H.2
-
17
-
-
0038495746
-
The DNA sequence of human chromosome 7
-
Hillier, L.W., Fulton, R.S., Fulton, L.A., Graves, T.A., Pepin, K.H., Wagner-McPherson, C., Layman, D., Maas, J., Jaeger, S., Walker, R., et al. 2003. The DNA sequence of human chromosome 7. Nature 424: 157-164.
-
(2003)
Nature
, vol.424
, pp. 157-164
-
-
Hillier, L.W.1
Fulton, R.S.2
Fulton, L.A.3
Graves, T.A.4
Pepin, K.H.5
Wagner-McPherson, C.6
Layman, D.7
Maas, J.8
Jaeger, S.9
Walker, R.10
-
18
-
-
33645611575
-
Heterozygotes for the microinversion of the Williams-Beuren syndrome region have an increased risk for affected offspring
-
ed. ASHG The American Journal of Human Genetics, Toronto
-
Hobart, H., Gregg, R., Mervis, C., Robinson, B., Kimberley, K., Rios, C., and Morris, C. 2004. Heterozygotes for the microinversion of the Williams-Beuren syndrome region have an increased risk for affected offspring. In 54th Annual Meeting of the ASHG (ed. ASHG), pp. 177. The American Journal of Human Genetics, Toronto.
-
(2004)
54th Annual Meeting of the ASHG
, pp. 177
-
-
Hobart, H.1
Gregg, R.2
Mervis, C.3
Robinson, B.4
Kimberley, K.5
Rios, C.6
Morris, C.7
-
19
-
-
0034849408
-
MRBAYES: Bayesian inference of phylogenetic trees
-
Huelsenbeck, J.P. and Ronquist, F. 2001. MRBAYES: Bayesian inference of phylogenetic trees. Bioinformatics 17: 754-755.
-
(2001)
Bioinformatics
, vol.17
, pp. 754-755
-
-
Huelsenbeck, J.P.1
Ronquist, F.2
-
20
-
-
0036139211
-
MEGA2: Molecular evolutionary genetics analysis software
-
Kumar, S., Tamura, K., Jakobsen, I.B., and Nei, M. 2001. MEGA2: Molecular evolutionary genetics analysis software. Bioinformatics 17: 1244-1245.
-
(2001)
Bioinformatics
, vol.17
, pp. 1244-1245
-
-
Kumar, S.1
Tamura, K.2
Jakobsen, I.B.3
Nei, M.4
-
21
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
Lander, E.S., Linton, L.M., Birren, B., Nusbaum, C., Zody, M.C., Baldwin, J., Devon, K., Dewar, K., Doyle, M., FitzHugh, W., et al. 2001. Initial sequencing and analysis of the human genome. Nature 409: 860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
Lander, E.S.1
Linton, L.M.2
Birren, B.3
Nusbaum, C.4
Zody, M.C.5
Baldwin, J.6
Devon, K.7
Dewar, K.8
Doyle, M.9
FitzHugh, W.10
-
22
-
-
14044265129
-
HIP1 (huntingtin interacting protein 1) regulates clathrin assembly through direct binding to the regulatory region of the clathrin light chain
-
Legendre-Guillemin, V., Metzler, M., Lemaire, J.F., Philie, J., Gan, L., Hayden, M.R., and McPherson, P.S. 2005. HIP1 (huntingtin interacting protein 1) regulates clathrin assembly through direct binding to the regulatory region of the clathrin light chain. J. Biol. Chem. 280: 6101-6108.
-
(2005)
J. Biol. Chem.
, vol.280
, pp. 6101-6108
-
-
Legendre-Guillemin, V.1
Metzler, M.2
Lemaire, J.F.3
Philie, J.4
Gan, L.5
Hayden, M.R.6
McPherson, P.S.7
-
23
-
-
0037350508
-
Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome
-
Liu, G., Zhao, S., Bailey, J.A., Sahinalp, S.C., Alkan, C., Tuzun, E., Green, E.D., and Eichler, E.E. 2003. Analysis of primate genomic variation reveals a repeat-driven expansion of the human genome. Genome Res. 13: 358-368.
-
(2003)
Genome Res.
, vol.13
, pp. 358-368
-
-
Liu, G.1
Zhao, S.2
Bailey, J.A.3
Sahinalp, S.C.4
Alkan, C.5
Tuzun, E.6
Green, E.D.7
Eichler, E.E.8
-
24
-
-
0037351987
-
Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization
-
Locke, D.P., Segraves, R., Carbone, L., Archidiacono, N., Albertson, D.G., Pinkel, D., and Eichler, E.E. 2003. Large-scale variation among human and great ape genomes determined by array comparative genomic hybridization. Genome Res. 13: 347-357.
-
(2003)
Genome Res.
, vol.13
, pp. 347-357
-
-
Locke, D.P.1
Segraves, R.2
Carbone, L.3
Archidiacono, N.4
Albertson, D.G.5
Pinkel, D.6
Eichler, E.E.7
-
25
-
-
4744345428
-
Chromosomal rearrangements and the genomic distribution of gene-expression divergence in humans and chimpanzees
-
Marques-Bonet, T., Caceres, M., Bertranpetit, J., Preuss, T.M., Thomas, J.W., and Navarro, A. 2004. Chromosomal rearrangements and the genomic distribution of gene-expression divergence in humans and chimpanzees. Trends Genet. 20: 524-529.
-
(2004)
Trends Genet.
, vol.20
, pp. 524-529
-
-
Marques-Bonet, T.1
Caceres, M.2
Bertranpetit, J.3
Preuss, T.M.4
Thomas, J.W.5
Navarro, A.6
-
26
-
-
3843145134
-
The evolutionary history of human chromosome 7
-
Muller, S., Finelli, P., Neusser, M., and Wienberg, J. 2004. The evolutionary history of human chromosome 7. Genomics 84: 458-467.
-
(2004)
Genomics
, vol.84
, pp. 458-467
-
-
Muller, S.1
Finelli, P.2
Neusser, M.3
Wienberg, J.4
-
27
-
-
0037432734
-
Chromosomal speciation and molecular divergence - Accelerated evolution in rearranged chromosomes
-
Navarro, A. and Barton, N.H. 2003. Chromosomal speciation and molecular divergence - Accelerated evolution in rearranged chromosomes. Science 300: 321-324.
-
(2003)
Science
, vol.300
, pp. 321-324
-
-
Navarro, A.1
Barton, N.H.2
-
29
-
-
0026446059
-
Transcription enhances intrachromosomal homologous recombination in mammalian cells
-
Nickoloff, J.A. 1992. Transcription enhances intrachromosomal homologous recombination in mammalian cells. Mol. Cell. Biol. 12: 5311-5318.
-
(1992)
Mol. Cell. Biol.
, vol.12
, pp. 5311-5318
-
-
Nickoloff, J.A.1
-
30
-
-
0028849441
-
Genomic organization of the human PMS2 gene family
-
Nicolaides, N.C., Carter, K.C., Shell, B.K., Papadopoulos, N., Vogelstein, B., and Kinzler, K.W. 1995. Genomic organization of the human PMS2 gene family. Genomics 30: 195-206.
-
(1995)
Genomics
, vol.30
, pp. 195-206
-
-
Nicolaides, N.C.1
Carter, K.C.2
Shell, B.K.3
Papadopoulos, N.4
Vogelstein, B.5
Kinzler, K.W.6
-
31
-
-
0030667669
-
PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7
-
Osborne, L.R., Herbrick, J.A., Greavette, T., Heng, H.H., Tsui, L.C., and Scherer, S.W. 1997. PMS2-related genes flank the rearrangement breakpoints associated with Williams syndrome and other diseases on human chromosome 7. Genomics 45: 402-406.
-
(1997)
Genomics
, vol.45
, pp. 402-406
-
-
Osborne, L.R.1
Herbrick, J.A.2
Greavette, T.3
Heng, H.H.4
Tsui, L.C.5
Scherer, S.W.6
-
32
-
-
0035179436
-
A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome
-
Osborne, L.R., Li, M., Pober, B., Chitayat, D., Bodurtha, J., Mandel, A., Costa, T., Grebe, T., Cox, S., Tsui, L.C., et al. 2001. A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome. Nat. Genet. 29: 321-325.
-
(2001)
Nat. Genet.
, vol.29
, pp. 321-325
-
-
Osborne, L.R.1
Li, M.2
Pober, B.3
Chitayat, D.4
Bodurtha, J.5
Mandel, A.6
Costa, T.7
Grebe, T.8
Cox, S.9
Tsui, L.C.10
-
33
-
-
0033939577
-
A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome - Deletion region at 7q11.23
-
Peoples, R., Franke, Y., Wang, Y.K., Pérez-Jurado, L., Paperna, T., Cisco, M., and Francke, U. 2000. A physical map, including a BAC/PAC clone contig, of the Williams-Beuren syndrome - Deletion region at 7q11.23. Am. J. Hum. Genet. 66: 47-68.
-
(2000)
Am. J. Hum. Genet.
, vol.66
, pp. 47-68
-
-
Peoples, R.1
Franke, Y.2
Wang, Y.K.3
Pérez-Jurado, L.4
Paperna, T.5
Cisco, M.6
Francke, U.7
-
34
-
-
0002391264
-
Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth
-
Pérez Jurado, L.A., Peoples, R., Kaplan, P., Hamel, B.C., and Francke, U. 1996. Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth. Am. J. Hum. Genet. 59: 781-792.
-
(1996)
Am. J. Hum. Genet.
, vol.59
, pp. 781-792
-
-
Pérez Jurado, L.A.1
Peoples, R.2
Kaplan, P.3
Hamel, B.C.4
Francke, U.5
-
35
-
-
0031886974
-
A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK
-
Pérez Jurado, L.A., Wang, Y.K., Peoples, R., Coloma, A., Cruces, J., and Francke, U. 1998. A duplicated gene in the breakpoint regions of the 7q11.23 Williams-Beuren syndrome deletion encodes the initiator binding protein TFII-I and BAP-135, a phosphorylation target of BTK. Hum. Mol. Genet. 7: 325-334.
-
(1998)
Hum. Mol. Genet.
, vol.7
, pp. 325-334
-
-
Pérez Jurado, L.A.1
Wang, Y.K.2
Peoples, R.3
Coloma, A.4
Cruces, J.5
Francke, U.6
-
36
-
-
0034011069
-
STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion
-
Pezzi, N., Prieto, I., Kremer, L., Pérez Jurado, L.A., Valero, C., Del Mazo, J., Martinez, A.C., and Barbero, J.L. 2000. STAG3, a novel gene encoding a protein involved in meiotic chromosome pairing and location of STAG3-related genes flanking the Williams-Beuren syndrome deletion. FASEB J. 14: 581-592.
-
(2000)
FASEB J.
, vol.14
, pp. 581-592
-
-
Pezzi, N.1
Prieto, I.2
Kremer, L.3
Pérez Jurado, L.A.4
Valero, C.5
Del Mazo, J.6
Martinez, A.C.7
Barbero, J.L.8
-
37
-
-
0000625869
-
Analyzing tables of statistical tests
-
Rice, W. 1989. Analyzing tables of statistical tests. Evolution 43: 223-225.
-
(1989)
Evolution
, vol.43
, pp. 223-225
-
-
Rice, W.1
-
38
-
-
0029891886
-
Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion
-
Robinson, W.P., Waslynka, J., Bernasconi, F., Wang, M., Clark, S., Kotzot, D., and Schinzel, A. 1996. Delineation of 7q11.2 deletions associated with Williams-Beuren syndrome and mapping of a repetitive sequence to within and to either side of the common deletion. Genomics 34: 17-23.
-
(1996)
Genomics
, vol.34
, pp. 17-23
-
-
Robinson, W.P.1
Waslynka, J.2
Bernasconi, F.3
Wang, M.4
Clark, S.5
Kotzot, D.6
Schinzel, A.7
-
39
-
-
0032972599
-
DnaSP version 3: An integrated program for molecular population genetics and molecular evolution analysis
-
Rozas, J. and Rozas, R. 1999. DnaSP version 3: An integrated program for molecular population genetics and molecular evolution analysis. Bioinformatics 15: 174-175.
-
(1999)
Bioinformatics
, vol.15
, pp. 174-175
-
-
Rozas, J.1
Rozas, R.2
-
40
-
-
0036245495
-
Segmental duplications and the evolution of the primate genome
-
Samonte, R.V. and Eichler, E.E. 2002. Segmental duplications and the evolution of the primate genome. Nat. Rev. Genet. 3: 65-72.
-
(2002)
Nat. Rev. Genet.
, vol.3
, pp. 65-72
-
-
Samonte, R.V.1
Eichler, E.E.2
-
41
-
-
0038756128
-
Human chromosome 7: DNA sequence and biology
-
Scherer, S.W., Cheung, J., MacDonald, J.R., Osborne, L.R., Nakabayashi, K., Herbrick, J.A., Carson, A.R., Parker-Katiraee, L., Skaug, J., Khaja, R., et al. 2003. Human chromosome 7: DNA sequence and biology. Science 300: 767-772.
-
(2003)
Science
, vol.300
, pp. 767-772
-
-
Scherer, S.W.1
Cheung, J.2
MacDonald, J.R.3
Osborne, L.R.4
Nakabayashi, K.5
Herbrick, J.A.6
Carson, A.R.7
Parker-Katiraee, L.8
Skaug, J.9
Khaja, R.10
-
42
-
-
0003402305
-
-
Genetics and Biometry Laboratory, University of Geneva, Switzerland
-
Schneider, S., Roessli, D., and Excoffier, L. 2000. Arlequin ver.2.000: A software for population genetics data analysis. Genetics and Biometry Laboratory, University of Geneva, Switzerland.
-
(2000)
Arlequin Ver.2.000: A Software for Population Genetics Data Analysis
-
-
Schneider, S.1
Roessli, D.2
Excoffier, L.3
-
43
-
-
0035746665
-
Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review
-
Shaikh, T.H., Kurahashi, H., and Emanuel, B.S. 2001. Evolutionarily conserved low copy repeats (LCRs) in 22q11 mediate deletions, duplications, translocations, and genomic instability: An update and literature review. Genet. Med. 3: 6-13.
-
(2001)
Genet. Med.
, vol.3
, pp. 6-13
-
-
Shaikh, T.H.1
Kurahashi, H.2
Emanuel, B.S.3
-
44
-
-
8744265059
-
Serial segmental duplications during primate evolution result in complex human genome architecture
-
Stankiewicz, P., Shaw, C.J., Withers, M., Inoue, K., and Lupski, J.R. 2004. Serial segmental duplications during primate evolution result in complex human genome architecture. Genome Res. 14: 2209-2220.
-
(2004)
Genome Res.
, vol.14
, pp. 2209-2220
-
-
Stankiewicz, P.1
Shaw, C.J.2
Withers, M.3
Inoue, K.4
Lupski, J.R.5
-
45
-
-
13944278863
-
A common inversion under selection in Europeans
-
Stefansson, H., Helgason, A., Thorleifsson, G., Steinthorsdottir, V., Masson, G., Barnard, J., Baker, A., Jonasdottir, A., Ingason, A., Gudnadottir, V.G., et al. 2005. A common inversion under selection in Europeans. Nat. Genet. 37: 129-137.
-
(2005)
Nat. Genet.
, vol.37
, pp. 129-137
-
-
Stefansson, H.1
Helgason, A.2
Thorleifsson, G.3
Steinthorsdottir, V.4
Masson, G.5
Barnard, J.6
Baker, A.7
Jonasdottir, A.8
Ingason, A.9
Gudnadottir, V.G.10
-
46
-
-
0027157960
-
Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees
-
Tamura, K. and Nei, M. 1993. Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol. Biol. Evol. 10: 512-526.
-
(1993)
Mol. Biol. Evol.
, vol.10
, pp. 512-526
-
-
Tamura, K.1
Nei, M.2
-
47
-
-
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. Nucleic Acids Res. 22: 4673-4680.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 4673-4680
-
-
Thompson, J.D.1
Higgins, D.G.2
Gibson, T.J.3
-
48
-
-
3342951462
-
Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome
-
Tipney, H.J., Hinsley, T.A., Brass, A., Metcalfe, K., Donnai, D., and Tassabehji, M. 2004. Isolation and characterisation of GTF2IRD2, a novel fusion gene and member of the TFII-I family of transcription factors, deleted in Williams-Beuren syndrome. Eur. J. Hum. Genet. 12: 551-560.
-
(2004)
Eur. J. Hum. Genet.
, vol.12
, pp. 551-560
-
-
Tipney, H.J.1
Hinsley, T.A.2
Brass, A.3
Metcalfe, K.4
Donnai, D.5
Tassabehji, M.6
-
49
-
-
0034306681
-
Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: The low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s)
-
Valero, M.C., de Luis, O., Cruces, J., and Pérez Jurado, L.A. 2000. Fine-scale comparative mapping of the human 7q11.23 region and the orthologous region on mouse chromosome 5G: The low-copy repeats that flank the Williams-Beuren syndrome deletion arose at breakpoint sites of an evolutionary inversion(s). Genomics 69: 1-13.
-
(2000)
Genomics
, vol.69
, pp. 1-13
-
-
Valero, M.C.1
De Luis, O.2
Cruces, J.3
Pérez Jurado, L.A.4
-
50
-
-
0032919063
-
CYS3, a hotspot of meiotic recombination in Saccharomyces cerevisiae. Effects of heterozygosity and mismatch repair functions on gene conversion and recombination intermediates
-
Vedel, M. and Nicolas, A. 1999. CYS3, a hotspot of meiotic recombination in Saccharomyces cerevisiae. Effects of heterozygosity and mismatch repair functions on gene conversion and recombination intermediates. Genetics 151: 1245-1259.
-
(1999)
Genetics
, vol.151
, pp. 1245-1259
-
-
Vedel, M.1
Nicolas, A.2
-
51
-
-
0035895505
-
The sequence of the human genome
-
Venter, J.C., Adams, M.D., Myers, E.W., Li, P.W., Mural, R.J., Sutton, G.G., Smith, H.O., Yandell, M., Evans, C.A., Holt, R.A., et al. 2001. The sequence of the human genome. Science 291: 1304-1351.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
Smith, H.O.7
Yandell, M.8
Evans, C.A.9
Holt, R.A.10
-
52
-
-
0020027910
-
The origin of man: A chromosomal pictorial legacy
-
Yunis, J.J. and Prakash, O. 1982. The origin of man: A chromosomal pictorial legacy. Science 215: 1525-1530.
-
(1982)
Science
, vol.215
, pp. 1525-1530
-
-
Yunis, J.J.1
Prakash, O.2
-
53
-
-
33645629624
-
-
NCBI home page
-
http://www.ncbi.nlm.nih.gov/; NCBI home page.
-
-
-
-
54
-
-
33645630055
-
-
The NIH Intramural Sequencing Center (NISC)
-
http://www.nisc.nih.gov/; The NIH Intramural Sequencing Center (NISC).
-
-
-
-
55
-
-
33645631414
-
-
Ensembl Genome Browser
-
http://www.ensembl.org/; Ensembl Genome Browser.
-
-
-
-
56
-
-
33645616652
-
-
UCSC Genome Browser Home
-
http://www.genome.ucsc.edu/; UCSC Genome Browser Home.
-
-
-
-
57
-
-
33645626884
-
-
Primer3 Input
-
http://frodo.wi.mit.edu/cgi-bin/primer3/primer3_www.cgi; Primer3 Input.
-
-
-
-
58
-
-
33645628644
-
-
RepeatMasker
-
http://www.repeatmasker.org/; RepeatMasker.
-
-
-
-
59
-
-
33645629368
-
-
The MAVID multiple alignment server
-
http://baboon.math.berkeley.edu/mavid/; The MAVID multiple alignment server.
-
-
-
|