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共有2340篇/ 每页显示10篇/ 目前第188页/ 共234页/ 首页前一页 179 180 181 182 183 184 185 186 187 188 后一页尾页

Candidate driver genes in focal chromosomal aberrations of stage II colon cancer. Brosens RPM, Haan JC, Carvalho B, Rustenburg F, Grabsch H, Quirke P, Engel AF, Cuesta MA, Maughan N, Flens M, Meijer GA, and Ylstra B. The Journal of pathology 221 (4), 411-424.Aug 2010

Trisomic dose of several chromosome 21 genes perturbs haematopoietic stem and progenitor cell differentiation in Down's syndrome. De Vita S, Canzonetta C, Mulligan C, Delom F, Groet J, Baldo C, Vanes L, Dagna-Bricarelli F, Hoischen A, Veltman J, Fisher EMC, Tybulewicz VLJ, and Nizetic D. Oncogene , -.9 Aug 2010

Large inverted repeats within Xp11.2 are present at the breakpoints of isodicentric X chromosomes in Turner syndrome Scott SA, Cohen N, Brandt T, Warburton PE, and Edelmann L. Human molecular genetics 19 (17), 3383-3393.1 Sep 2010

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk. Antonacci F, Kidd J, Marques-Bonet T, Teague B, Ventura M, Girirajan S, Alkan C, Campbell C, Vives L, Malig M, Rosenfeld J, Ballif B, Shaffer L, Graves T, Wilson R, Schwartz D, and Eichler E. Nature genetics 42 (9), 745-750.Sep 2010

Gene amplification as double minutes or homogeneously staining regions in solid tumors Storlazzi C, Lonoce A, Guastadisegni M, Trombetta D, D'Addabbo P, Daniele G, L'Abbate A, Macchia G, Surace C, Kok K, Ullmann R, Purgato S, Palumbo O, Carella M, Ambros P, and Rocchi M. Genome Res. 20 (9), 1198-1206.1 Sep 2010

Recurrent 200-kb deletions of 16p11.2 that include the SH2B1 gene are associated with developmental delay and obesity. Bachmann-Gagescu R, Mefford HC, Cowan C, Glew GM, Hing AV, Wallace S, Bader PI, Hamati A, Reitnauer PJ, Smith R, Stockton DW, Muhle H, Helbig I, Eichler EE, Ballif BC, Rosenfeld J, and Tsuchiya KD. Genetics in medicine : official journal of the American College of Medical Genetics 12 (10), 641-647.Oct 2010

Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia. Vacic V, McCarthy S, Malhotra D, Murray F, Chou H, Peoples A, Makarov V, Yoon S, Bhandari A, Corominas R, Iakoucheva L, Krastoshevsky O, Krause V, Larach-Walters V, Welsh D, Craig D, Kelsoe J, Gershon E, Leal S, Aquila MD, Morris D, Gill M, Corvin A, Insel P, McClellan J, King M, Karayiorgou M, Levy D, DeLisi L, and Sebat J. Nature advance online publication (7339), 499-503.23 Feb 2011

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. Norton N, Li D, Rieder MJ, Siegfried JD, Rampersaud E, Z¨¹chner S, Mangos S, Gonzalez-Quintana J, Wang L, McGee S, Reiser J, Martin E, Nickerson DA, and Hershberger RE. American journal of human genetics 88 (3), 273-282.11 Mar 2011

Performance assessment of copy number microarray platforms using a spike-in experiment Halper-Stromberg E, Frelin L, Ruczinski I, Scharpf R, Jie C, Carvalho B, Hao H, Hetrick K, Jedlicka A, Dziedzic A, Doheny K, Scott A, Baylin S, Pevsner J, Spencer F, and Irizarry R. Bioinformatics 27 (8), -.15 Apr 2011

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency. Ochalski ME, Engle N, Wakim A, Ravnan BJ, Hoffner L, Rajkovic A, and Surti U. Fertility and sterility , -.28 Apr 2011

共有2340篇/ 每页显示10篇/ 目前第188页/ 共234页/ 首页前一页 179 180 181 182 183 184 185 186 187 188 后一页尾页

2012年影响因子智能查询系统(2011年度)

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