-
1
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei I. A, Schmidt S, Peshkin L, Ramensky VE, Gerasimova A, Bork P, Kondrashov A. S, Sunyaev SR. 2010. A method and server for predicting damaging missense mutations. Nat Methods 7: 248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
Ramensky, V.E.4
Gerasimova, A.5
Bork, P.6
Kondrashov, A.S.7
Sunyaev, S.R.8
-
2
-
-
37249032200
-
Accurate prediction of the functional significance of single nucleotide polymorphisms and mutations in the ABCA1 gene
-
Brunham L. R, Singaraja RR, Pape TD, Kejariwal A, Thomas PD, Hayden MR. 2005. Accurate prediction of the functional significance of single nucleotide polymorphisms and mutations in the ABCA1 gene. PLoS Genetics 1: e83.
-
(2005)
PLoS Genetics
, vol.1
-
-
Brunham, L.R.1
Singaraja, R.R.2
Pape, T.D.3
Kejariwal, A.4
Thomas, P.D.5
Hayden, M.R.6
-
3
-
-
33746829957
-
DNA microarray technologies for measuring protein-DNA interactions
-
Bulyk M.L. 2006. DNA microarray technologies for measuring protein-DNA interactions. Curr Opin Biotechnol 17: 422-430.
-
(2006)
Curr Opin Biotechnol
, vol.17
, pp. 422-430
-
-
Bulyk, M.L.1
-
4
-
-
44349191457
-
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
-
Campbell P. J, Stephens PJ, Pleasance ED, O'Meara S, Li H, Santarius T, Stebbings L. A, Leroy C, Edkins S, Hardy C, et al. 2008. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genetics 40: 722-729.
-
(2008)
Nat Genetics
, vol.40
, pp. 722-729
-
-
Campbell, P.J.1
Stephens, P.J.2
Pleasance, E.D.3
O'Meara, S.4
Li, H.5
Santarius, T.6
Stebbings, L.A.7
Leroy, C.8
Edkins, S.9
Hardy, C.10
-
5
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
Cancer Genome Atlas Research Network
-
Cancer Genome Atlas Research Network. 2008. Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 455: 1061-1068.
-
(2008)
Nature
, vol.455
, pp. 1061-1068
-
-
-
6
-
-
69549116107
-
BreakDancer: An algorithm for high-resolution mapping of genomic structural variation
-
Chen K., Wallis JW, McLellan MD, Larson DE, Kalicki JM, Pohl CS, McGrath SD, Wendl MC, Zhang Q, Locke DP, et al. 2009. BreakDancer: An algorithm for high-resolution mapping of genomic structural variation. Nat Methods 6: 677-681.
-
(2009)
Nat Methods
, vol.6
, pp. 677-681
-
-
Chen, K.1
Wallis, J.W.2
McLellan, M.D.3
Larson, D.E.4
Kalicki, J.M.5
Pohl, C.S.6
McGrath, S.D.7
Wendl, M.C.8
Zhang, Q.9
Locke, D.P.10
-
7
-
-
41149121347
-
The evolution of mammalian gene families
-
Demuth J. P, De Bie T, Stajich JE, Cristianini N, Hahn MW. 2006. The evolution of mammalian gene families. PLoS ONE 1: e85.
-
(2006)
PLoS ONE
, vol.1
-
-
Demuth, J.P.1
De Bie, T.2
Stajich, J.E.3
Cristianini, N.4
Hahn, M.W.5
-
8
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, et al. 2011. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genetics 43: 491-498.
-
(2011)
Nat Genetics
, vol.43
, pp. 491-498
-
-
DePristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
Philippakis, A.A.7
del Angel, G.8
Rivas, M.A.9
Hanna, M.10
-
9
-
-
84871809302
-
STAR: Ultrafast universal RNA-seq aligner
-
Dobin A., Davis CA, Schlesinger F, Drenkow J, Zaleski C, Jha S, Batut P, Chaisson M., Gingeras TR. 2013. STAR: Ultrafast universal RNA-seq aligner. Bioinformatics 29: 15-21.
-
(2013)
Bioinformatics
, vol.29
, pp. 15-21
-
-
Dobin, A.1
Davis, C.A.2
Schlesinger, F.3
Drenkow, J.4
Zaleski, C.5
Jha, S.6
Batut, P.7
Chaisson, M.8
Gingeras, T.R.9
-
10
-
-
84875391572
-
Ensembl 2013
-
Flicek P., Ahmed I, Amode MR, Barrell D, Beal K, Brent S, Carvalho-Silva D, Clapham P., Coates G, Fairley S, et al. 2013. Ensembl 2013. Nucleic Acids Res 41: D48-D55.
-
(2013)
Nucleic Acids Res
, vol.41
-
-
Flicek, P.1
Ahmed, I.2
Amode, M.R.3
Barrell, D.4
Beal, K.5
Brent, S.6
Carvalho-Silva, D.7
Clapham, P.8
Coates, G.9
Fairley, S.10
-
11
-
-
34548217651
-
Maximizing mouse cancer models
-
Frese K. K, Tuveson DA. 2007. Maximizing mouse cancer models. Nat Rev Cancer 7: 645-658.
-
(2007)
Nat Rev Cancer
, vol.7
, pp. 645-658
-
-
Frese, K.K.1
Tuveson, D.A.2
-
12
-
-
0037417884
-
Comparison of mouse and human genomes followed by experimental verification yields an estimated 1,019 additional genes
-
Guigo R., Dermitzakis ET, Agarwal P, Ponting CP, Parra G, Reymond A, Abril JF, Keibler E, Lyle R, Ucla C, et al. 2003. Comparison of mouse and human genomes followed by experimental verification yields an estimated 1,019 additional genes. Proc Natl Acad Sci 100: 1140-1145.
-
(2003)
Proc Natl Acad Sci
, vol.100
, pp. 1140-1145
-
-
Guigo, R.1
Dermitzakis, E.T.2
Agarwal, P.3
Ponting, C.P.4
Parra, G.5
Reymond, A.6
Abril, J.F.7
Keibler, E.8
Lyle, R.9
Ucla, C.10
-
13
-
-
33644874573
-
The UCSC Genome Browser Database: Update 2006
-
Hinrichs A. S, Karolchik D, Baertsch R, Barber GP, Bejerano G, Clawson H, Diekhans M., Furey TS, Harte RA, Hsu F, et al. 2006. The UCSC Genome Browser Database: Update 2006. Nucleic Acids Res 34: D590-D598.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Hinrichs, A.S.1
Karolchik, D.2
Baertsch, R.3
Barber, G.P.4
Bejerano, G.5
Clawson, H.6
Diekhans, M.7
Furey, T.S.8
Harte, R.A.9
Hsu, F.10
-
14
-
-
84864258996
-
A landscape of driver mutations in melanoma
-
Hodis E., Watson IR, Kryukov GV, Arold ST, Imielinski M, Theurillat JP, Nickerson E., Auclair D, Li L, Place C, et al. 2012. A landscape of driver mutations in melanoma. Cell 150: 251-263.
-
(2012)
Cell
, vol.150
, pp. 251-263
-
-
Hodis, E.1
Watson, I.R.2
Kryukov, G.V.3
Arold, S.T.4
Imielinski, M.5
Theurillat, J.P.6
Nickerson, E.7
Auclair, D.8
Li, L.9
Place, C.10
-
15
-
-
84897418427
-
Section E.6-Quality standards of samples
-
International Cancer Genome Consortium, In
-
International Cancer Genome Consortium. 2010. Section E.6-Quality standards of samples. In Updates to goals, structure, policies & guidelines. http://icgc.org/icgc/goals-structure-policies-guidelines.
-
(2010)
Updates to goals, structure, policies & guidelines
-
-
-
16
-
-
77951115122
-
International network of cancer genome projects
-
International Cancer Genome Consortium
-
International Cancer Genome Consortium, Hudson TJ, Anderson W, Artez A, Barker AD, Bell C, Bernabe RR, Bhan MK, Calvo F, Eerola I, et al. 2010. International network of cancer genome projects. Nature 464: 993-998.
-
(2010)
Nature
, vol.464
, pp. 993-998
-
-
Hudson, T.J.1
Anderson, W.2
Artez, A.3
Barker, A.D.4
Bell, C.5
Bernabe, R.R.6
Bhan, M.K.7
Calvo, F.8
Eerola, I.9
-
17
-
-
7244245762
-
Finishing the euchromatic sequence of the human genome
-
International Human Genome Sequencing Consortium
-
International Human Genome Sequencing Consortium. 2004. Finishing the euchromatic sequence of the human genome. Nature 431: 931-945.
-
(2004)
Nature
, vol.431
, pp. 931-945
-
-
-
18
-
-
80052851950
-
Mouse genomic variation and its effect on phenotypes and gene regulation
-
Keane T. M, Goodstadt L, Danecek P, White MA, Wong K, Yalcin B, Heger A, Agam A, Slater G, Goodson M, et al. 2011. Mouse genomic variation and its effect on phenotypes and gene regulation. Nature 477: 289-294.
-
(2011)
Nature
, vol.477
, pp. 289-294
-
-
Keane, T.M.1
Goodstadt, L.2
Danecek, P.3
White, M.A.4
Wong, K.5
Yalcin, B.6
Heger, A.7
Agam, A.8
Slater, G.9
Goodson, M.10
-
19
-
-
84863229597
-
VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing
-
Koboldt D. C, Zhang Q, Larson DE, Shen D, McLellan MD, Lin L, Miller CA, Mardis E. R, Ding L, Wilson RK. 2012. VarScan 2: Somatic mutation and copy number alteration discovery in cancer by exome sequencing. Genome Res 22: 568-576.
-
(2012)
Genome Res
, vol.22
, pp. 568-576
-
-
Koboldt, D.C.1
Zhang, Q.2
Larson, D.E.3
Shen, D.4
McLellan, M.D.5
Lin, L.6
Miller, C.A.7
Mardis, E.R.8
Ding, L.9
Wilson, R.K.10
-
20
-
-
33344463202
-
Independent expansion of the keratin gene family in teleostean fish and mammals: An insight from phylogenetic analysis and radiation hybrid mapping of keratin genes in zebrafish
-
Krushna Padhi B, Akimenko MA, Ekker M. 2006. Independent expansion of the keratin gene family in teleostean fish and mammals: An insight from phylogenetic analysis and radiation hybrid mapping of keratin genes in zebrafish. Gene 368: 37-45.
-
(2006)
Gene
, vol.368
, pp. 37-45
-
-
Krushna Padhi, B.1
Akimenko, M.A.2
Ekker, M.3
-
21
-
-
84874810955
-
From binding motifs in ChIP-Seq data to improved models of transcription factor binding sites
-
Kulakovskiy I., Levitsky V, Oshchepkov D, Bryzgalov L, Vorontsov I, Makeev V. 2013. From binding motifs in ChIP-Seq data to improved models of transcription factor binding sites. J Bioinform Comput Biol 11: 1340004.
-
(2013)
J Bioinform Comput Biol
, vol.11
, pp. 1340004
-
-
Kulakovskiy, I.1
Levitsky, V.2
Oshchepkov, D.3
Bryzgalov, L.4
Vorontsov, I.5
Makeev, V.6
-
22
-
-
84856565531
-
SomaticSniper: Identification of somatic point mutations in whole genome sequencing data
-
Larson D. E, Harris CC, Chen K, Koboldt DC, Abbott TE, Dooling DJ, Ley TJ, Mardis E. R, Wilson RK, Ding L. 2012. SomaticSniper: Identification of somatic point mutations in whole genome sequencing data. Bioinformatics 28: 311-317.
-
(2012)
Bioinformatics
, vol.28
, pp. 311-317
-
-
Larson, D.E.1
Harris, C.C.2
Chen, K.3
Koboldt, D.C.4
Abbott, T.E.5
Dooling, D.J.6
Ley, T.J.7
Mardis, E.R.8
Wilson, R.K.9
Ding, L.10
-
23
-
-
80054915847
-
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data
-
Li H. 2011. A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data. Bioinformatics 27: 2987-2993.
-
(2011)
Bioinformatics
, vol.27
, pp. 2987-2993
-
-
Li, H.1
-
24
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
Li H., Durbin R. 2009. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 25: 1754-1760.
-
(2009)
Bioinformatics
, vol.25
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
25
-
-
84871447495
-
Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing
-
Lu S., Zong C, Fan W, Yang M, Li J, Chapman AR, Zhu P, Hu X, Xu L, Yan L, et al. 2012. Probing meiotic recombination and aneuploidy of single sperm cells by whole-genome sequencing. Science 338: 1627-1630.
-
(2012)
Science
, vol.338
, pp. 1627-1630
-
-
Lu, S.1
Zong, C.2
Fan, W.3
Yang, M.4
Li, J.5
Chapman, A.R.6
Zhu, P.7
Hu, X.8
Xu, L.9
Yan, L.10
-
26
-
-
34250863886
-
Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers
-
Maser R. S, Choudhury B, Campbell PJ, Feng B, Wong KK, Protopopov A, O'Neil J, Gutierrez A, Ivanova E, Perna I, et al. 2007. Chromosomally unstable mouse tumours have genomic alterations similar to diverse human cancers. Nature 447: 966-971.
-
(2007)
Nature
, vol.447
, pp. 966-971
-
-
Maser, R.S.1
Choudhury, B.2
Campbell, P.J.3
Feng, B.4
Wong, K.K.5
Protopopov, A.6
O'Neil, J.7
Gutierrez, A.8
Ivanova, E.9
Perna, I.10
-
27
-
-
1542563409
-
Initial sequencing and comparative analysis of the mouse genome
-
Mouse Genome Sequencing Consortium
-
Mouse Genome Sequencing Consortium, Waterston RH, Lindblad-Toh K, Birney E., Rogers J, Abril JF, Agarwal P, Agarwala R, Ainscough R, Alexandersson M., et al. 2002. Initial sequencing and comparative analysis of the mouse genome. Nature 420: 520-562.
-
(2002)
Nature
, vol.420
, pp. 520-562
-
-
Waterston, R.H.1
Lindblad-Toh, K.2
Birney, E.3
Rogers, J.4
Abril, J.F.5
Agarwal, P.6
Agarwala, R.7
Ainscough, R.8
Alexandersson, M.9
-
28
-
-
0035026704
-
Predicting deleterious amino acid substitutions
-
Ng P. C, Henikoff S. 2001. Predicting deleterious amino acid substitutions. Genome Res 11: 863-874.
-
(2001)
Genome Res
, vol.11
, pp. 863-874
-
-
Ng, P.C.1
Henikoff, S.2
-
29
-
-
13444256478
-
Inparanoid: A comprehensive database of eukaryotic orthologs
-
O'Brien KP, Remm M, Sonnhammer EL. 2005. Inparanoid: A comprehensive database of eukaryotic orthologs. Nucleic Acids Res 33: D476-D480.
-
(2005)
Nucleic Acids Res
, vol.33
-
-
O'Brien, K.P.1
Remm, M.2
Sonnhammer, E.L.3
-
30
-
-
70349312354
-
ChIP-seq: Advantages and challenges of a maturing technology
-
Park P.J. 2009. ChIP-seq: Advantages and challenges of a maturing technology. Nat Rev Genetics 10: 669-680.
-
(2009)
Nat Rev Genetics
, vol.10
, pp. 669-680
-
-
Park, P.J.1
-
31
-
-
77951860138
-
Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome
-
Quinlan A. R, Clark RA, Sokolova S, Leibowitz ML, Zhang Y, Hurles ME, Mell J. C, Hall IM. 2010. Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome. Genome Res 20: 623-635.
-
(2010)
Genome Res
, vol.20
, pp. 623-635
-
-
Quinlan, A.R.1
Clark, R.A.2
Sokolova, S.3
Leibowitz, M.L.4
Zhang, Y.5
Hurles, M.E.6
Mell, J.C.7
Hall, I.M.8
-
33
-
-
4344646902
-
Species-and cell type-specific requirements for cellular transformation
-
Rangarajan A., Hong SJ, Gifford A, Weinberg RA. 2004. Species-and cell type-specific requirements for cellular transformation. Cancer Cell 6: 171-183.
-
(2004)
Cancer Cell
, vol.6
, pp. 171-183
-
-
Rangarajan, A.1
Hong, S.J.2
Gifford, A.3
Weinberg, R.A.4
-
34
-
-
0034646331
-
The olfactory receptor gene repertoire in primates and mouse: Evidence for reduction of the functional fraction in primates
-
Rouquier S., Blancher A, Giorgi D. 2000. The olfactory receptor gene repertoire in primates and mouse: Evidence for reduction of the functional fraction in primates. Proc Natl Acad Sci 97: 2870-2874.
-
(2000)
Proc Natl Acad Sci
, vol.97
, pp. 2870-2874
-
-
Rouquier, S.1
Blancher, A.2
Giorgi, D.3
-
36
-
-
84861576201
-
The landscape of cancer genes and mutational processes in breast cancer
-
Stephens P. J, Tarpey PS, Davies H, Van Loo P, Greenman C, Wedge DC, Nik-Zainal S, Martin S, Varela I, Bignell GR, et al. 2012. The landscape of cancer genes and mutational processes in breast cancer. Nature 486: 400-404.
-
(2012)
Nature
, vol.486
, pp. 400-404
-
-
Stephens, P.J.1
Tarpey, P.S.2
Davies, H.3
Van Loo, P.4
Greenman, C.5
Wedge, D.C.6
Nik-Zainal, S.7
Martin, S.8
Varela, I.9
Bignell, G.R.10
-
37
-
-
84862293682
-
A simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods
-
Sultan M., Dokel S, Amstislavskiy V, Wuttig D, Sultmann H, Lehrach H, Yaspo M.L. 2012. A simple strand-specific RNA-Seq library preparation protocol combining the Illumina TruSeq RNA and the dUTP methods. Biochem Biophys Res Commun 422: 643-646.
-
(2012)
Biochem Biophys Res Commun
, vol.422
, pp. 643-646
-
-
Sultan, M.1
Dokel, S.2
Amstislavskiy, V.3
Wuttig, D.4
Sultmann, H.5
Lehrach, H.6
Yaspo, M.L.7
-
39
-
-
65449136284
-
TopHat: Discovering splice junctions with RNA-Seq
-
Trapnell C., Pachter L, Salzberg SL. 2009. TopHat: Discovering splice junctions with RNA-Seq. Bioinformatics 25: 1105-1111.
-
(2009)
Bioinformatics
, vol.25
, pp. 1105-1111
-
-
Trapnell, C.1
Pachter, L.2
Salzberg, S.L.3
-
40
-
-
77957732035
-
Somatic structural rearrangements in genetically engineered mouse mammary tumors
-
Varela I., Klijn C, Stephens PJ, Mudie LJ, Stebbings L, Galappaththige D, van der Gulden H, Schut E, Klarenbeek S, Campbell PJ, et al. 2010. Somatic structural rearrangements in genetically engineered mouse mammary tumors. Genome Biology 11: R100.
-
(2010)
Genome Biology
, vol.11
-
-
Varela, I.1
Klijn, C.2
Stephens, P.J.3
Mudie, L.J.4
Stebbings, L.5
Galappaththige, D.6
van der Gulden, H.7
Schut, E.8
Klarenbeek, S.9
Campbell, P.J.10
-
41
-
-
57749195712
-
RNA-Seq: A revolutionary tool for transcriptomics
-
Wang Z., Gerstein M, Snyder M. 2009. RNA-Seq: A revolutionary tool for transcriptomics. Nat Rev Genetics 10: 57-63.
-
(2009)
Nat Rev Genetics
, vol.10
, pp. 57-63
-
-
Wang, Z.1
Gerstein, M.2
Snyder, M.3
-
42
-
-
79953299687
-
Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression
-
Wartman L. D, Larson DE, Xiang Z, Ding L, Chen K, Lin L, Cahan P, Klco JM, Welch J. S, Li C, et al. 2011. Sequencing a mouse acute promyelocytic leukemia genome reveals genetic events relevant for disease progression. J Clin Invest 121: 1445-1455.
-
(2011)
J Clin Invest
, vol.121
, pp. 1445-1455
-
-
Wartman, L.D.1
Larson, D.E.2
Xiang, Z.3
Ding, L.4
Chen, K.5
Lin, L.6
Cahan, P.7
Klco, J.M.8
Welch, J.S.9
Li, C.10
-
44
-
-
78650663859
-
Enhanced structural variant and breakpoint detection using SVMerge by integration of multiple detection methods and local assembly
-
Wong K., Keane TM, Stalker J, Adams DJ. 2010. Enhanced structural variant and breakpoint detection using SVMerge by integration of multiple detection methods and local assembly. Genome Biol 11: R128.
-
(2010)
Genome Biol
, vol.11
-
-
Wong, K.1
Keane, T.M.2
Stalker, J.3
Adams, D.J.4
-
45
-
-
84865219405
-
Sequencing and characterization of the FVB/NJ mouse genome
-
Wong K., Bumpstead S, Van Der Weyden L, Reinholdt LG, Wilming LG, Adams D. J, Keane TM. 2012. Sequencing and characterization of the FVB/NJ mouse genome. Genome Biol 13: R72.
-
(2012)
Genome Biol
, vol.13
-
-
Wong, K.1
Bumpstead, S.2
Van Der Weyden, L.3
Reinholdt, L.G.4
Wilming, L.G.5
Adams, D.J.6
Keane, T.M.7
-
46
-
-
84865076224
-
Genomic variation in the vomeronasal receptor gene repertoires of inbred mice
-
Wynn E. H, Sanchez-Andrade G, Carss KJ, Logan DW. 2012. Genomic variation in the vomeronasal receptor gene repertoires of inbred mice. BMC Genomics 13: 415.
-
(2012)
BMC Genomics
, vol.13
, pp. 415
-
-
Wynn, E.H.1
Sanchez-Andrade, G.2
Carss, K.J.3
Logan, D.W.4
-
47
-
-
84855401988
-
International Cancer Genome Consortium Data Portal-A one-stop shop for cancer genomics data
-
bar026
-
Zhang J., Baran J, Cros A, Guberman JM, Haider S, Hsu J, Liang Y, Rivkin E, Wang J., Whitty B, et al. 2011. International Cancer Genome Consortium Data Portal-A one-stop shop for cancer genomics data. Database 2011: bar026.
-
(2011)
Database 2011
-
-
Zhang, J.1
Baran, J.2
Cros, A.3
Guberman, J.M.4
Haider, S.5
Hsu, J.6
Liang, Y.7
Rivkin, E.8
Wang, J.9
Whitty, B.10
-
48
-
-
84871461434
-
Genome-wide detection of singlenucleotide and copy-number variations of a single human cell
-
Zong C., Lu S, Chapman AR, Xie XS. 2012. Genome-wide detection of singlenucleotide and copy-number variations of a single human cell. Science 338: 1622-1626.
-
(2012)
Science
, vol.338
, pp. 1622-1626
-
-
Zong, C.1
Lu, S.2
Chapman, A.R.3
Xie, X.S.4
|