-
1
-
-
0020158239
-
Immunological method for mapping genes on Drosophila polytene chromosomes
-
Langer-Safer PR, Levine M, Ward DC. Immunological method for mapping genes on Drosophila polytene chromosomes. Proc Natl Acad Sci USA 1982;79:4381-4385.
-
(1982)
Proc Natl Acad Sci USA
, vol.79
, pp. 4381-4385
-
-
Langer-Safer, P.R.1
Levine, M.2
Ward, D.C.3
-
2
-
-
0022446922
-
Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization
-
Pinkel D, Straume T, Gray JW. Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 1986;83:2934-2938.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Straume, T.2
Gray, J.W.3
-
3
-
-
0027185655
-
Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome
-
Ewart AK, Morris CA, Atkinson D, Jin W, Sternes K, Spallone P et al. Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome. Nat Genet 1993;5:11-16.
-
(1993)
Nat Genet
, vol.5
, pp. 11-16
-
-
Ewart, A.K.1
Morris, C.A.2
Atkinson, D.3
Jin, W.4
Sternes, K.5
Spallone, P.6
-
4
-
-
0025868571
-
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
-
Lupski JR, de Oca-Luna RM, Slaugenhaupt S, Pentao L, Guzzetta V, Trask BJ et al. DNA duplication associated with Charcot-Marie-Tooth disease type 1A. Cell 1991; 66:219-232.
-
(1991)
Cell
, vol.66
, pp. 219-232
-
-
Lupski, J.R.1
De Oca-Luna, R.M.2
Slaugenhaupt, S.3
Pentao, L.4
Guzzetta, V.5
Trask, B.J.6
-
5
-
-
0028798545
-
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
-
Flint J, Wilkie AOM, Buckle VJ, Winter RM, Holland AJ, McDermid HE. The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nat Genet 1995;9:132-140.
-
(1995)
Nat Genet
, vol.9
, pp. 132-140
-
-
Flint, J.1
Aom, W.2
Buckle, V.J.3
Winter, R.M.4
Holland, A.J.5
McDermid, H.E.6
-
6
-
-
0033851883
-
An optimized set of human telomere clones for studying telomere integrity and architecture
-
Knight SJ, Lese CM, Precht KS, Kuc J, Ning Y, Lucas S et al. An optimized set of human telomere clones for studying telomere integrity and architecture. Am J Hum Genet 2000;67:320-332.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 320-332
-
-
Knight, S.J.1
Lese, C.M.2
Precht, K.S.3
Kuc, J.4
Ning, Y.5
Lucas, S.6
-
7
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F et al. Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 1992;258:818-821.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
Kallioniemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
-
8
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H et al. Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chromosomes Cancer 1997;20:399-407.
-
(1997)
Genes Chromosomes Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
-
9
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders AM, Nowak N, Segraves R, Blackwood S, Brown N, Conroy J et al. Assembly of microarrays for genome-wide measurement of DNA copy number. Nat Genet 2001;29:263-264.
-
(2001)
Nat Genet
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
-
10
-
-
0035252636
-
High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH
-
Bruder CE, Hirvela C, Tapia-Paez I, Fransson I, Segraves R, Hamilton G et al. High resolution deletion analysis of constitutional DNA from neurofibromatosis type 2 (NF2) patients using microarray-CGH. Hum Mol Genet 2001;10:271-282.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 271-282
-
-
Bruder, C.E.1
Hirvela, C.2
Tapia-Paez, I.3
Fransson, I.4
Segraves, R.5
Hamilton, G.6
-
11
-
-
0041867866
-
Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection
-
Mantripragada KK, Buckley PG, Jarbo C, Menzel U, Dumanski JP. Development of NF2 gene specific, strictly sequence defined diagnostic microarray for deletion detection. J Mol Med 2003;81:443-451.
-
(2003)
J Mol Med
, vol.81
, pp. 443-451
-
-
Mantripragada, K.K.1
Buckley, P.G.2
Jarbo, C.3
Menzel, U.4
Dumanski, J.P.5
-
12
-
-
0037677609
-
Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH
-
Veltman JA, Jonkers Y, Nuijten I, Janssen I, van d V, Huys E et al. Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGH. Am J Hum Genet 2003;72:1578-1584.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1578-1584
-
-
Veltman, J.A.1
Jonkers, Y.2
Nuijten, I.3
Janssen, I.4
Van, D.V.5
Huys, E.6
-
13
-
-
18344379676
-
High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization
-
Veltman JA, Schoenmakers EF, Eussen BH, Janssen I, Merkx G, van Cleef B et al. High-throughput analysis of subtelomeric chromosome rearrangements by use of array-based comparative genomic hybridization. Am J Hum Genet 2002;70:1269-1276.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1269-1276
-
-
Veltman, J.A.1
Schoenmakers, E.F.2
Eussen, B.H.3
Janssen, I.4
Merkx, G.5
Van Cleef, B.6
-
14
-
-
1542721515
-
BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications
-
Locke DP, Segraves R, Nicholls RD, Schwartz S, Pinkel D, Albertson DG et al. BAC microarray analysis of 15q11-q13 rearrangements and the impact of segmental duplications. J Med Genet 2004;41:175-182.
-
(2004)
J Med Genet
, vol.41
, pp. 175-182
-
-
Locke, D.P.1
Segraves, R.2
Nicholls, R.D.3
Schwartz, S.4
Pinkel, D.5
Albertson, D.G.6
-
15
-
-
18144445946
-
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications
-
Buckley PG, Mantripragada KK, Benetkiewicz M, Tapia-Paez I, Diaz DS, Rosenquist M et al. A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications. Hum Mol Genet 2002;11:3221-3229.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 3221-3229
-
-
Buckley, P.G.1
Mantripragada, K.K.2
Benetkiewicz, M.3
Tapia-Paez, I.4
Diaz, D.S.5
Rosenquist, M.6
-
16
-
-
2942729593
-
High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation
-
Veltman JA, Yntema HG, Lugtenberg D, Arts H, Briault S, Huys EH et al. High resolution profiling of X chromosomal aberrations by array comparative genomic hybridisation. J Med Genet 2004;41:425-432.
-
(2004)
J Med Genet
, vol.41
, pp. 425-432
-
-
Veltman, J.A.1
Yntema, H.G.2
Lugtenberg, D.3
Arts, H.4
Briault, S.5
Huys, E.H.6
-
17
-
-
9144240478
-
Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities
-
Vissers LE, de Vries BB, Osoegawa K, Janssen IM, Feuth T, Choy CO et al. Array-Based Comparative Genomic Hybridization for the Genomewide Detection of Submicroscopic Chromosomal Abnormalities. Am J Hum Genet 2003;73:1261-1270.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1261-1270
-
-
Vissers, L.E.1
De Vries, B.B.2
Osoegawa, K.3
Janssen, I.M.4
Feuth, T.5
Choy, C.O.6
-
18
-
-
11144356173
-
Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features
-
Shaw-Smith C, Redon R, Rickman L, Rio M, Willatt L, Fiegler H et al. Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features. J Med Genet 2004;41:241-248.
-
(2004)
J Med Genet
, vol.41
, pp. 241-248
-
-
Shaw-Smith, C.1
Redon, R.2
Rickman, L.3
Rio, M.4
Willatt, L.5
Fiegler, H.6
-
19
-
-
10744233914
-
A tiling resolution DNA microarray with complete coverage of the human genome
-
Ishkanian AS, Malloff CA, Watson SK, DeLeeuw RJ, Chi B, Coe BP et al. A tiling resolution DNA microarray with complete coverage of the human genome. Nat Genet 2004;36:299-303.
-
(2004)
Nat Genet
, vol.36
, pp. 299-303
-
-
Ishkanian, A.S.1
Malloff, C.A.2
Watson, S.K.3
Deleeuw, R.J.4
Chi, B.5
Coe, B.P.6
-
20
-
-
4444239112
-
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome
-
Vissers LE, van Ravenswaaij CM, Admiraal R, Hurst JA, de Vries BB, Janssen IM et al. Mutations in a new member of the chromodomain gene family cause CHARGE syndrome. Nat Genet 2004;36:955-957.
-
(2004)
Nat Genet
, vol.36
, pp. 955-957
-
-
Vissers, L.E.1
Van Ravenswaaij, C.M.2
Admiraal, R.3
Hurst, J.A.4
De Vries, B.B.5
Janssen, I.M.6
-
21
-
-
0036218046
-
Genome-wide detection of chromosomal imbalances in tumors using BAG microarrays
-
Cai WW, Mao JH, Chow CW, Damani S, Balmain A, Bradley A. Genome-wide detection of chromosomal imbalances in tumors using BAG microarrays. Nat Biotechnol 2002;20:393-396.
-
(2002)
Nat Biotechnol
, vol.20
, pp. 393-396
-
-
Cai, W.W.1
Mao, J.H.2
Chow, C.W.3
Damani, S.4
Balmain, A.5
Bradley, A.6
-
22
-
-
10744221541
-
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions
-
Yu W, Ballif BC, Kashork CD, Heilstedt HA, Howard LA, Cai WW et al. Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions. Hum Mol Genet 2003;12:2145-2152.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2145-2152
-
-
Yu, W.1
Ballif, B.C.2
Kashork, C.D.3
Heilstedt, H.A.4
Howard, L.A.5
Cai, W.W.6
-
23
-
-
1242269840
-
Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders
-
Shaw CJ, Shaw CA, Yu W, Stankiewicz P, White LD, Beaudet AL et al. Comparative genomic hybridisation using a proximal 17p BAC/PAC array detects rearrangements responsible for four genomic disorders. J Med Genet 2004;41:113-119.
-
(2004)
J Med Genet
, vol.41
, pp. 113-119
-
-
Shaw, C.J.1
Shaw, C.A.2
Yu, W.3
Stankiewicz, P.4
White, L.D.5
Beaudet, A.L.6
-
24
-
-
16044371402
-
A complete set of human telomeric probes and their clinical application
-
National Institutes of Health and Institute of Molecular Medicine collaboration
-
Ning Y, Roschke A, Smith ACM, Macha M, Precht K, Riethman H et al. A complete set of human telomeric probes and their clinical application. National Institutes of Health and Institute of Molecular Medicine collaboration. Nat Genet 1996;14:86-89.
-
(1996)
Nat Genet
, vol.14
, pp. 86-89
-
-
Ning, Y.1
Roschke, A.2
Acm, S.3
Macha, M.4
Precht, K.5
Riethman, H.6
-
25
-
-
0038392953
-
The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation
-
Flint J, Knight S. The use of telomere probes to investigate submicroscopic rearrangements associated with mental retardation. Curr Opin Genet Dev 2003;13:10-16.
-
(2003)
Curr Opin Genet Dev
, vol.13
, pp. 10-16
-
-
Flint, J.1
Knight, S.2
-
26
-
-
2342593128
-
An orderly retreat: Dedifferentiation is a regulated process
-
Katoh M, Shaw C, Xu Q, Van Driessche N, Morio T, Kuwayama H et al. An orderly retreat: Dedifferentiation is a regulated process. Proc Natl Acad Sci USA 2004;101: 7005-7010.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 7005-7010
-
-
Katoh, M.1
Shaw, C.2
Xu, Q.3
Van Driessche, N.4
Morio, T.5
Kuwayama, H.6
-
27
-
-
0037316303
-
A comparison of normalization methods for high density oligonucleotide array data based on variance and bias
-
Bolstad BM, Irizarry RA, Astrand M, Speed TP. A comparison of normalization methods for high density oligonucleotide array data based on variance and bias. Bioinformatics 2003;19:185-193.
-
(2003)
Bioinformatics
, vol.19
, pp. 185-193
-
-
Bolstad, B.M.1
Irizarry, R.A.2
Astrand, M.3
Speed, T.P.4
-
28
-
-
1342294092
-
Normalization for cDNA microarray data: A robust composite method addressing single and multiple slide systematic variation
-
Yang YH. Normalization for cDNA microarray data: A robust composite method addressing single and multiple slide systematic variation. Nucleic Acids Res 2002;30: e15.
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Yang, Y.H.1
-
29
-
-
0025729359
-
Fluorescence in situ hybridization: Applications in cytogenetics and gene mapping
-
Trask BJ. Fluorescence in situ hybridization: Applications in cytogenetics and gene mapping. Trends Genet 1991;7:149-154.
-
(1991)
Trends Genet
, vol.7
, pp. 149-154
-
-
Trask, B.J.1
-
30
-
-
0036590015
-
FISH-mapping of a 100-kb terminal 22q13 deletion
-
Anderlid BM, Schoumans J, Anneren G, Tapia-Paez I, Dumanski J, Blennow E et al. FISH-mapping of a 100-kb terminal 22q13 deletion. Hum Genet 2002;110:439-443.
-
(2002)
Hum Genet
, vol.110
, pp. 439-443
-
-
Anderlid, B.M.1
Schoumans, J.2
Anneren, G.3
Tapia-Paez, I.4
Dumanski, J.5
Blennow, E.6
-
31
-
-
0029087828
-
Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization
-
Guo WJ, Callif-Daley F, Zapata MC, Miller ME. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization. Am J Med Genet 1995;58:230-236.
-
(1995)
Am J Med Genet
, vol.58
, pp. 230-236
-
-
Guo, W.J.1
Callif-Daley, F.2
Zapata, M.C.3
Miller, M.E.4
-
32
-
-
0035071955
-
Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements
-
Giglio S, Broman KW, Matsumoto N, Calvari V, Gimelli G, Neumann T et al. Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements. Am J 0Hum Genet 2001;68:874-883.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 874-883
-
-
Giglio, S.1
Broman, K.W.2
Matsumoto, N.3
Calvari, V.4
Gimelli, G.5
Neumann, T.6
-
33
-
-
0347766009
-
Mapping and initial analysis of human subtelomeric sequence assemblies
-
Riethman H, Ambrosini A, Castaneda C, Finklestein J, Hu XL, Mudunuri U et al. Mapping and initial analysis of human subtelomeric sequence assemblies. Genome Res 2004;14:18-28.
-
(2004)
Genome Res
, vol.14
, pp. 18-28
-
-
Riethman, H.1
Ambrosini, A.2
Castaneda, C.3
Finklestein, J.4
Hu, X.L.5
Mudunuri, U.6
-
34
-
-
0033361765
-
Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints
-
Amos-Landgraf JM, Ji Y, Gottlieb W, Depinet T, Wandstrat AE, Cassidy SB et al. Chromosome breakage in the Prader-Willi and Angelman syndromes involves recombination between large, transcribed repeats at proximal and distal breakpoints. Am J Hum Genet 1999;65:370-386.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 370-386
-
-
Amos-Landgraf, J.M.1
Ji, Y.2
Gottlieb, W.3
Depinet, T.4
Wandstrat, A.E.5
Cassidy, S.B.6
-
35
-
-
0028128516
-
Healing of broken human chromosomes by the addition of telomeric repeats
-
Flint J, Craddock CF, Villegas A, Bentley DP, Williams HJ, Galanello R et al. Healing of broken human chromosomes by the addition of telomeric repeats. Am J Hum Genet 1994;55:505-512.
-
(1994)
Am J Hum Genet
, vol.55
, pp. 505-512
-
-
Flint, J.1
Craddock, C.F.2
Villegas, A.3
Bentley, D.P.4
Williams, H.J.5
Galanello, R.6
-
36
-
-
0036988394
-
Stabilization of a terminal inversion duplication of 8p by telomere capture from 18q
-
Kostiner DR, Nguyen H, Cox VA, Cotter PD. Stabilization of a terminal inversion duplication of 8p by telomere capture from 18q. Cytogenet Genome Res 2002;98:9-12.
-
(2002)
Cytogenet Genome Res
, vol.98
, pp. 9-12
-
-
Kostiner, D.R.1
Nguyen, H.2
Cox, V.A.3
Cotter, P.D.4
-
37
-
-
0032929028
-
An 18q-syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA
-
Katz SG, Schneider SS, Bartuski A, Trask BJ, Massa H, Overhauser J et al. An 18q-syndrome breakpoint resides between the duplicated serpins SCCA1 and SCCA2 and arises via a cryptic rearrangement with satellite III DNA. Hum Mol Genet 1999; 8:87-92.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 87-92
-
-
Katz, S.G.1
Schneider, S.S.2
Bartuski, A.3
Trask, B.J.4
Massa, H.5
Overhauser, J.6
-
38
-
-
0033838428
-
Characterization of terminal deletions at 7q32 and 22q13.3 healed by de novo telomere addition
-
Varley H, Di S, Scherer SW, Royle NJ. Characterization of terminal deletions at 7q32 and 22q13.3 healed by De novo telomere addition. Am J Hum Genet 2000;67:610-622.
-
(2000)
Am J Hum Genet
, vol.67
, pp. 610-622
-
-
Varley, H.1
Di, S.2
Scherer, S.W.3
Royle, N.J.4
-
39
-
-
0042329928
-
Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: Cytogenetic, molecular, and clinical analyses of 32 new observations
-
Luciani JJ, de Mas P, Depetris D, Mignon-Ravix C, Bottani A, Prieur M et al. Telomeric 22q13 deletions resulting from rings, simple deletions, and translocations: cytogenetic, molecular, and clinical analyses of 32 new observations. J Med Genet 2003;40:690-696.
-
(2003)
J Med Genet
, vol.40
, pp. 690-696
-
-
Luciani, J.J.1
De Mas, P.2
Depetris, D.3
Mignon-Ravix, C.4
Bottani, A.5
Prieur, M.6
-
40
-
-
3242808027
-
Large-scale copy number polymorphism in the human genome
-
Sebat J, Lakshmi B, Troge J, Alexander J, Young J, Lundin P et al. Large-scale copy number polymorphism in the human genome. Science 2004;305:525-528.
-
(2004)
Science
, vol.305
, pp. 525-528
-
-
Sebat, J.1
Lakshmi, B.2
Troge, J.3
Alexander, J.4
Young, J.5
Lundin, P.6
-
41
-
-
3543040014
-
Complex SNP-related sequence variation in segmental genome duplications
-
Fredman D, White SJ, Potter S, Eichler EE, den Dunnen JT, Brookes AJ. Complex SNP-related sequence variation in segmental genome duplications. Nat Genet 2004; 36:861-866.
-
(2004)
Nat Genet
, vol.36
, pp. 861-866
-
-
Fredman, D.1
White, S.J.2
Potter, S.3
Eichler, E.E.4
Den Dunnen, J.T.5
Brookes, A.J.6
-
42
-
-
4444291843
-
Detection of large-scale variation in the human genome
-
Iafrate AJ, Feuk L, Rivera MN, Listewnik ML, Donahoe PK, Qi Y et al. Detection of large-scale variation in the human genome. Nat Genet 2004;36:949-951.
-
(2004)
Nat Genet
, vol.36
, pp. 949-951
-
-
Iafrate, A.J.1
Feuk, L.2
Rivera, M.N.3
Listewnik, M.L.4
Donahoe, P.K.5
Qi, Y.6
-
43
-
-
4444375366
-
As normal as normal can be?
-
Carter NP. As normal as normal can be? Nat Genet 2004;36:931-932.
-
(2004)
Nat Genet
, vol.36
, pp. 931-932
-
-
Carter, N.P.1
-
44
-
-
5444250990
-
Applications of genomic microarrays to explore human chromosome structure and function
-
Carter NP, Vetrie D. Applications of genomic microarrays to explore human chromosome structure and function. Hum Mol Genet 2004;13 Spec No 2:R297-R302.
-
(2004)
Hum Mol Genet
, vol.13
, Issue.SPEC. NO. 2
-
-
Carter, N.P.1
Vetrie, D.2
-
45
-
-
10744231187
-
Representational oligonucleotide microarray analysis: A high-resolution method to detect genome copy number variation
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Lucito R, Healy J, Alexander J, Reiner A, Esposito D, Chi M et al. Representational oligonucleotide microarray analysis: a high-resolution method to detect genome copy number variation. Genome Res 2003;13:2291-2305.
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(2003)
Genome Res
, vol.13
, pp. 2291-2305
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Lucito, R.1
Healy, J.2
Alexander, J.3
Reiner, A.4
Esposito, D.5
Chi, M.6
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