-
1
-
-
34249815834
-
FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity
-
DOI 10.1038/ng2046, PII NG2046
-
Fanciulli M, et al. (2007) FCGR3B copy number variation is associatedwith susceptibility to systemic, but not organ-specific, autoimmunity. Nat Genet 39:721-723. (Pubitemid 46848593)
-
(2007)
Nature Genetics
, vol.39
, Issue.6
, pp. 721-723
-
-
Fanciulli, M.1
Norsworthy, P.J.2
Petretto, E.3
Dong, R.4
Harper, L.5
Kamesh, L.6
Heward, J.M.7
Gough, S.C.L.8
De Smith, A.9
Blakemore, A.I.F.10
Froguel, P.11
Owen, C.J.12
Pearce, S.H.S.13
Teixeira, L.14
Guillevin, L.15
Graham, D.S.C.16
Pusey, C.D.17
Cook, H.T.18
Vyse, T.J.19
Aitman, T.J.20
more..
-
2
-
-
34247481814
-
Strong association of de novo copy number mutations with autism
-
DOI 10.1126/science.1138659
-
Sebat J, et al. (2007) Strong association of de novo copy number mutations with autism. Science 316:445-449. (Pubitemid 46651493)
-
(2007)
Science
, vol.316
, Issue.5823
, pp. 445-449
-
-
Sebat, J.1
Lakshmi, B.2
Malhotra, D.3
Troge, J.4
Lese-Martin, C.5
Walsh, T.6
Yamrom, B.7
Yoon, S.8
Krasnitz, A.9
Kendall, J.10
Leotta, A.11
Pai, D.12
Zhang, R.13
Lee, Y.-H.14
Hicks, J.15
Spence, S.J.16
Lee, A.T.17
Puura, K.18
Lehtimaki, T.19
Ledbetter, D.20
Gregersen, P.K.21
Bregman, J.22
Sutcliffe, J.S.23
Jobanputra, V.24
Chung, W.25
Warburton, D.26
King, M.-C.27
Skuse, D.28
Geschwind, D.H.29
Gilliam, T.C.30
Ye, K.31
Wigler, M.32
more..
-
3
-
-
51649107017
-
Rare chromosomal deletions and duplications increase risk of schizophrenia
-
Stone J, et al. (2008) Rare chromosomal deletions and duplications increase risk of schizophrenia. Nature 455:237-241.
-
(2008)
Nature
, vol.455
, pp. 237-241
-
-
Stone, J.1
-
4
-
-
49949085933
-
Large recurrent microdeletions associated with schizophrenia
-
Stefansson H, et al. (2008) Large recurrent microdeletions associated with schizophrenia. Nature 455:232-236.
-
(2008)
Nature
, vol.455
, pp. 232-236
-
-
Stefansson, H.1
-
5
-
-
76249116215
-
A new highly penetrant form of obesity due to deletions on chromosome 16p11
-
Walters R, et al. (2010) A new highly penetrant form of obesity due to deletions on chromosome 16p11. Nature 463:671-675.
-
(2010)
Nature
, vol.463
, pp. 671-675
-
-
Walters, R.1
-
6
-
-
76349083132
-
Large, rare chromosomal deletions associated with severe early-onset obesity
-
Bochukova E, et al. (2010) Large, rare chromosomal deletions associated with severe early-onset obesity. Nature 463:666-670.
-
(2010)
Nature
, vol.463
, pp. 666-670
-
-
Bochukova, E.1
-
7
-
-
69149100639
-
Acquired copy number alterations in adult acute myeloid leukemia genomes
-
Walter M, et al. (2009) Acquired copy number alterations in adult acute myeloid leukemia genomes. Proc Natl Acad Sci USA 106:12950-12955.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 12950-12955
-
-
Walter, M.1
-
8
-
-
20144368274
-
High-resolution genome-wide mapping of genetic alterations in human glial brain tumors
-
DOI 10.1158/0008-5472.CAN-04-4229
-
Bredel M, et al. (2005) High-resolution genome-wide mapping of genetic alterations in human glial brain tumors. Cancer Res 65:4088-4096. (Pubitemid 40775645)
-
(2005)
Cancer Research
, vol.65
, Issue.10
, pp. 4088-4096
-
-
Bredel, M.1
Bredel, C.2
Juric, D.3
Harsh, G.R.4
Vogel, H.5
Recht, L.D.6
Sikic, B.I.7
-
9
-
-
77249119762
-
The landscape of somatic copy-number alteration across human cancers
-
Beroukhim R, et al. (2010) The landscape of somatic copy-number alteration across human cancers. Nature 463:899-905.
-
(2010)
Nature
, vol.463
, pp. 899-905
-
-
Beroukhim, R.1
-
10
-
-
77249123407
-
Signatures of mutation and selection in the cancer genome
-
Bignell G, et al. (2010) Signatures of mutation and selection in the cancer genome. Nature 463:893-898.
-
(2010)
Nature
, vol.463
, pp. 893-898
-
-
Bignell, G.1
-
11
-
-
33751329250
-
Global variation in copy number in the human genome
-
DOI 10.1038/nature05329, PII NATURE05329
-
Redon R, et al. (2006) Global variation in copy number in the human genome. Nature 444:444-454. (Pubitemid 44809057)
-
(2006)
Nature
, vol.444
, Issue.7118
, pp. 444-454
-
-
Redon, R.1
Ishikawa, S.2
Fitch, K.R.3
Feuk, L.4
Perry, G.H.5
Andrews, T.D.6
Fiegler, H.7
Shapero, M.H.8
Carson, A.R.9
Chen, W.10
Cho, E.K.11
Dallaire, S.12
Freeman, J.L.13
Gonzalez, J.R.14
Gratacos, M.15
Huang, J.16
Kalaitzopoulos, D.17
Komura, D.18
MacDonald, J.R.19
Marshall, C.R.20
Mei, R.21
Montgomery, L.22
Nishimura, K.23
Okamura, K.24
Shen, F.25
Somerville, M.J.26
Tchinda, J.27
Valsesia, A.28
Woodwark, C.29
Yang, F.30
Zhang, J.31
Zerjal, T.32
Zhang, J.33
Armengol, L.34
Conrad, D.F.35
Estivill, X.36
Tyler-Smith, C.37
Carter, N.P.38
Aburatani, H.39
Lee, C.40
Jones, K.W.41
Scherer, S.W.42
Hurles, M.E.43
more..
-
12
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll S, et al. (2008) Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40:1166-1174.
-
(2008)
Nat Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.1
-
13
-
-
40549122972
-
Profiling of copy number variations (CNVS) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array
-
DOI 10.1002/humu.20659
-
Díaz de Ståhl T, et al. (2008) Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 K BAC-clone-based array. Hum Mutat 29:398-408. (Pubitemid 351364942)
-
(2008)
Human Mutation
, vol.29
, Issue.3
, pp. 398-408
-
-
Diaz, D.S.T.1
Sandgren, J.2
Piotrowski, A.3
Nord, H.4
Andersson, R.5
Menzel, U.6
Bogdan, A.7
Thuresson, A.-C.8
Poplawski, A.9
Von Teil, D.10
Hansson, C.M.11
Elshafie, A.I.12
ElGhazali, G.13
Imreh, S.14
Nordenskjold, M.15
Upadhyaya, M.16
Komorowski, J.17
Bruder, C.E.G.18
Dumanski, J.P.19
-
14
-
-
35448992970
-
Germ-line DNA copy number variation frequencies in a large North American population
-
DOI 10.1007/s00439-007-0404-5
-
Zogopoulos G, et al. (2007) Germ-line DNA copy number variation frequencies in a large North American population. Hum Genet 122:345-353. (Pubitemid 47616542)
-
(2007)
Human Genetics
, vol.122
, Issue.3-4
, pp. 345-353
-
-
Zogopoulos, G.1
Ha, K.C.H.2
Naqib, F.3
Moore, S.4
Kim, H.5
Montpetit, A.6
Robidoux, F.7
Laflamme, P.8
Cotterchio, M.9
Greenwood, C.10
Scherer, S.W.11
Zanke, B.12
Hudson, T.J.13
Bader, G.D.14
Gallinger, S.15
-
15
-
-
69749121852
-
High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications
-
Shaikh T, et al. (2009) High-resolution mapping and analysis of copy number variations in the human genome: A data resource for clinical and research applications. Genome Res 19:1682-1690.
-
(2009)
Genome Res
, vol.19
, pp. 1682-1690
-
-
Shaikh, T.1
-
16
-
-
62649088108
-
Population analysis of large copy number variants and hotspots of human genetic disease
-
Itsara A, et al. (2009) Population analysis of large copy number variants and hotspots of human genetic disease. Am J Hum Genet 84:148-161.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 148-161
-
-
Itsara, A.1
-
17
-
-
66349083341
-
A geometric approach for classification and comparison of structural variants
-
Sindi S, Helman E, Bashir A, Raphael B (2009) A geometric approach for classification and comparison of structural variants. Bioinformatics 25:i222-230.
-
(2009)
Bioinformatics
, vol.25
-
-
Sindi, S.1
Helman, E.2
Bashir, A.3
Raphael, B.4
-
18
-
-
67650064593
-
Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes
-
Hormozdiari F, Alkan C, Eichler E, Sahinalp S (2009) Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes. Genome Res 19:1270-1278.
-
(2009)
Genome Res
, vol.19
, pp. 1270-1278
-
-
Hormozdiari, F.1
Alkan, C.2
Eichler, E.3
Sahinalp, S.4
-
19
-
-
69549116107
-
BreakDancer: An algorithm for high-resolution mapping of genomic structural variation
-
Chen K, 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
-
20
-
-
70449704529
-
Computational methods for discovering structural variation with next-generation sequencing
-
Medvedev P, Stanciu M, Brudno M (2009) Computational methods for discovering structural variation with next-generation sequencing. Nat Methods 6:S13-S20.
-
(2009)
Nat Methods
, vol.6
-
-
Medvedev, P.1
Stanciu, M.2
Brudno, M.3
-
21
-
-
22844451617
-
Fine-scale structural variation of the human genome
-
DOI 10.1038/ng1562
-
Tuzun E, et al. (2005) Fine-scale structural variation of the human genome. Nat Genet 37:727-732. (Pubitemid 41754889)
-
(2005)
Nature Genetics
, vol.37
, Issue.7
, pp. 727-732
-
-
Tuzun, E.1
Sharp, A.J.2
Bailey, J.A.3
Kaul, R.4
Morrison, V.A.5
Pertz, L.M.6
Haugen, E.7
Hayden, H.8
Albertson, D.9
Pinkel, D.10
Olson, M.V.11
Eichler, E.E.12
-
22
-
-
58149218240
-
High-resolution mapping of copy-number alterations with massively parallel sequencing
-
Chiang D, et al. (2008) High-resolution mapping of copy-number alterations with massively parallel sequencing. Nat Methods 6:99-103.
-
(2008)
Nat Methods
, vol.6
, pp. 99-103
-
-
Chiang, D.1
-
23
-
-
64849083125
-
CNV-seq, a new method to detect copy number variation using high-throughput sequencing
-
Xie C, Tammi M (2009) CNV-seq, a new method to detect copy number variation using high-throughput sequencing. BMC Bioinformatics 10:80.
-
(2009)
BMC Bioinformatics
, vol.10
, pp. 80
-
-
Xie, C.1
Tammi, M.2
-
24
-
-
27544483495
-
Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data
-
DOI 10.1093/bioinformatics/bti611
-
Lai W, Johnson M, Kucherlapati R, Park P (2005) Comparative analysis of algorithms for identifying amplifications and deletions in array CGH data. Bioinformatics 21:3763-3770. (Pubitemid 41535525)
-
(2005)
Bioinformatics
, vol.21
, Issue.19
, pp. 3763-3770
-
-
Lai, W.R.1
Johnson, M.D.2
Kucherlapati, R.3
Park, P.J.4
-
25
-
-
55549097836
-
Mapping short DNA sequencing reads and calling variants using mapping quality scores
-
Li H, Ruan J, Durbin R (2008) Mapping short DNA sequencing reads and calling variants using mapping quality scores. Genome Res 18:1851-1858.
-
(2008)
Genome Res
, vol.18
, pp. 1851-1858
-
-
Li, H.1
Ruan, J.2
Durbin, R.3
-
26
-
-
62349130698
-
Ultrafast and memory-efficient alignment of short DNA sequences to the human genome
-
Langmead B, Trapnell C, Pop M, Salzberg S (2009) Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol 10:R25.
-
(2009)
Genome Biol
, vol.10
-
-
Langmead, B.1
Trapnell, C.2
Pop, M.3
Salzberg, S.4
-
27
-
-
77949587649
-
Fast and accurate long-read alignment with Burrows-Wheeler transform
-
Li H, Durbin R (2010) Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 26:589-595.
-
(2010)
Bioinformatics
, vol.26
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
28
-
-
0000120766
-
Estimating the dimension of a model
-
Schwarz G (1978) Estimating the dimension of a model. Ann Stat 6:461-464.
-
(1978)
Ann Stat
, vol.6
, pp. 461-464
-
-
Schwarz, G.1
-
29
-
-
0015475519
-
Symmetric binary B-trees: Data structure and maintenance algorithms
-
Bayer R (1972) Symmetric binary B-trees: Data structure and maintenance algorithms. Acta Inf 1:290-306.
-
(1972)
Acta Inf
, vol.1
, pp. 290-306
-
-
Bayer, R.1
-
30
-
-
84950758368
-
The calculation of posterior distributions by data augmentation
-
Tanner M, Wong W (1987) The calculation of posterior distributions by data augmentation. J Am Stat Assoc 82:528-540.
-
(1987)
J Am Stat Assoc
, vol.82
, pp. 528-540
-
-
Tanner, M.1
Wong, W.2
-
31
-
-
84950453304
-
Sampling-based approaches to calculating marginal densities
-
Gelfand A, Smith A (1990) Sampling-based approaches to calculating marginal densities. J Am Stat Assoc 85:398-409.
-
(1990)
J Am Stat Assoc
, vol.85
, pp. 398-409
-
-
Gelfand, A.1
Smith, A.2
-
32
-
-
1542515338
-
A census of human cancer genes
-
Futreal P, et al. (2004) A census of human cancer genes. Nat Rev Cancer 4:177-183. (Pubitemid 38337497)
-
(2004)
Nature Reviews Cancer
, vol.4
, Issue.3
, pp. 177-183
-
-
Futreal, P.A.1
Coin, L.2
Marshall, M.3
Down, T.4
Hubbard, T.5
Wooster, R.6
Rahman, N.7
Stratton, M.R.8
-
33
-
-
54549108740
-
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
-
McLendon R, et al. (2008) Comprehensive genomic characterization defines human glioblastoma genes and core pathways. Nature 455:1061-1068.
-
(2008)
Nature
, vol.455
, pp. 1061-1068
-
-
McLendon, R.1
-
34
-
-
62449252775
-
Oncogenic EGFR signaling cooperates with loss of tumor suppressor gene functions in gliomagenesis
-
Zhu H, et al. (2009) Oncogenic EGFR signaling cooperates with loss of tumor suppressor gene functions in gliomagenesis. Proc Natl Acad Sci USA 106:2712-2716.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 2712-2716
-
-
Zhu, H.1
-
35
-
-
7244238000
-
ADAM12 is selectively overexpressed in human glioblastomas and is associated with glioblastoma cell proliferation and shedding of heparin-binding epidermal growth factor
-
Kodama T, et al. (2004) ADAM12 is selectively overexpressed in human glioblastomas and is associatedwith glioblastoma cell proliferation and shedding of heparin-binding epidermal growth factor. Am J Pathol 165:1743-1753. (Pubitemid 39435171)
-
(2004)
American Journal of Pathology
, vol.165
, Issue.5
, pp. 1743-1753
-
-
Kodama, T.1
Ikeda, E.2
Okada, A.3
Ohtsuka, T.4
Shimoda, M.5
Shiomi, T.6
Yoshida, K.7
Nakada, M.8
Ohuchi, E.9
Okada, Y.10
-
36
-
-
0034626988
-
Inactivation of the DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents
-
Esteller M, et al. (2000) Inactivation of the DNA-repair gene MGMT and the clinical response of gliomas to alkylating agents. N Engl J Med 343:1350-1354.
-
(2000)
N Engl J Med
, vol.343
, pp. 1350-1354
-
-
Esteller, M.1
-
37
-
-
79951993228
-
O-Methylguanine-DNA methyltransferase (MGMT) mRNA expression predicts outcome in malignant glioma independent of MGMT promoter methylation
-
Kreth S, et al. (2011) O-Methylguanine-DNA methyltransferase (MGMT) mRNA expression predicts outcome in malignant glioma independent of MGMT promoter methylation. PLoS One 6:e17156.
-
(2011)
PLoS One
, vol.6
-
-
Kreth, S.1
-
38
-
-
77950475617
-
Mixed lineage leukemia: Roles in gene expression, hormone signaling and mRNA processing
-
Ansari K, Mandal S (2010) Mixed lineage leukemia: Roles in gene expression, hormone signaling and mRNA processing. FEBS J 277:1790-1804.
-
(2010)
FEBS J
, vol.277
, pp. 1790-1804
-
-
Ansari, K.1
Mandal, S.2
-
39
-
-
79251629946
-
The genetic landscape of the childhood cancer medulloblastoma
-
Parsons D, et al. (2010) The genetic landscape of the childhood cancer medulloblastoma. Science 331:435-439.
-
(2010)
Science
, vol.331
, pp. 435-439
-
-
Parsons, D.1
-
40
-
-
80051665475
-
Somatic mutations of the mixed-lineage leukemia 3 (MLL3) gene in primary breast cancers
-
Wang X, et al. (2011) Somatic mutations of the mixed-lineage leukemia 3 (MLL3) gene in primary breast cancers. Pathol Oncol Res 17:429-433.
-
(2011)
Pathol Oncol Res
, vol.17
, pp. 429-433
-
-
Wang, X.1
-
41
-
-
34248547564
-
Novel somatic and germline mutations in cancer candidate genes in glioblastoma, melanoma, and pancreatic carcinoma
-
DOI 10.1158/0008-5472.CAN-07-0065
-
Balakrishnan A, et al. (2007) Novel somatic and germline mutations in cancer candidate genes in glioblastoma, melanoma, and pancreatic carcinoma. Cancer Res 67:3545-3550. (Pubitemid 46762135)
-
(2007)
Cancer Research
, vol.67
, Issue.8
, pp. 3545-3550
-
-
Balakrishnan, A.1
Bleeker, F.E.2
Lamba, S.3
Rodolfo, M.4
Daniotti, M.5
Scarpa, A.6
Van Tilborg, A.A.7
Leenstra, S.8
Zanon, C.9
Bardelli, A.10
-
42
-
-
77951533670
-
AMY2A: A possible tumor-suppressor gene of 1p21. 1 loss in gastric carcinoma
-
Kang J, Koo S, Kwon K, Park J (2010) AMY2A: A possible tumor-suppressor gene of 1p21. 1 loss in gastric carcinoma. Int J Oncol 36:1429-1435.
-
(2010)
Int J Oncol
, vol.36
, pp. 1429-1435
-
-
Kang, J.1
Koo, S.2
Kwon, K.3
Park, J.4
-
43
-
-
77956593962
-
Second generation sequencing of the mesothelioma tumor genome
-
Bueno R, et al. (2010) Second generation sequencing of the mesothelioma tumor genome. PLoS One 5:e10612.
-
(2010)
PLoS One
, vol.5
-
-
Bueno, R.1
-
44
-
-
55549101623
-
DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome
-
Ley T, et al. (2008) DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome. Nature 456:66-72.
-
(2008)
Nature
, vol.456
, pp. 66-72
-
-
Ley, T.1
-
45
-
-
70149093912
-
Recurring mutations found by sequencing an acute myeloid leukemia genome
-
Mardis E, et al. (2009) Recurring mutations found by sequencing an acute myeloid leukemia genome. N Engl J Med 361:1058-1066.
-
(2009)
N Engl J Med
, vol.361
, pp. 1058-1066
-
-
Mardis, E.1
-
46
-
-
77955715121
-
Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML
-
Dicker F, et al. (2010) Mutation analysis for RUNX1, MLL-PTD, FLT3-ITD, NPM1 and NRAS in 269 patients with MDS or secondary AML. Leukemia 24:1528-1532.
-
(2010)
Leukemia
, vol.24
, pp. 1528-1532
-
-
Dicker, F.1
-
47
-
-
0026433031
-
Bowling plexopathy
-
Shukla A, Green J (1991) Bowling plexopathy. N Engl J Med 324:928-928.
-
(1991)
N Engl J Med
, vol.324
, pp. 928-928
-
-
Shukla, A.1
Green, J.2
-
48
-
-
54949137701
-
MetaSim: A sequencing simulator for genomics and metagenomics
-
Richter D, Ott F, Auch A, Schmid R, Huson D (2008) MetaSim: A sequencing simulator for genomics and metagenomics. PLoS One 3:e3373.
-
(2008)
PLoS One
, vol.3
-
-
Richter, D.1
Ott, F.2
Auch, A.3
Schmid, R.4
Huson, D.5
-
49
-
-
38049100456
-
Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma
-
Beroukhim R, et al. (2007) Assessing the significance of chromosomal aberrations in cancer: Methodology and application to glioma. Proc Natl Acad Sci USA 104:20007-20012.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 20007-20012
-
-
Beroukhim, R.1
-
50
-
-
84975804424
-
Mapping copy number variation by population-scale genome sequencing
-
Mills R, et al. (2011) Mapping copy number variation by population-scale genome sequencing. Nature 470:59-65.
-
(2011)
Nature
, vol.470
, pp. 59-65
-
-
Mills, R.1
-
51
-
-
79952194317
-
Discovery and genotyping of genome structural polymorphism by sequencing on a population scale
-
Handsaker R, Korn J, Nemesh J, McCarroll S (2011) Discovery and genotyping of genome structural polymorphism by sequencing on a population scale. Nat Genet 43:269-276.
-
(2011)
Nat Genet
, vol.43
, pp. 269-276
-
-
Handsaker, R.1
Korn, J.2
Nemesh, J.3
McCarroll, S.4
-
52
-
-
3543105225
-
Circular binary segmentation for the analysis of array-based DNA copy number data
-
DOI 10.1093/biostatistics/kxh008
-
Olshen AB, Venkatraman ES, Lucito R, Wigler M (2004) Circular binary segmentation for the analysis of array-based DNA copy number data. Biostatistics 5:557-572. (Pubitemid 41180205)
-
(2004)
Biostatistics
, vol.5
, Issue.4
, pp. 557-572
-
-
Olshen, A.B.1
Venkatraman, E.S.2
Lucito, R.3
Wigler, M.4
-
53
-
-
0033990048
-
Primer3 on the WWW for general users and for biologist programmers
-
Rozen S, Skaletsky H (2000) Primer3 on the WWW for general users and for biologist programmers. Methods Mol Biol 132:365-386.
-
(2000)
Methods Mol Biol
, vol.132
, pp. 365-386
-
-
Rozen, S.1
Skaletsky, H.2
|