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Items: 1 to 20 of 360

1.

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M.

Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4534-9. Epub 2006 Mar 14.

2.

High-resolution analysis of DNA copy number using oligonucleotide microarrays.

Bignell GR, Huang J, Greshock J, Watt S, Butler A, West S, Grigorova M, Jones KW, Wei W, Stratton MR, Futreal PA, Weber B, Shapero MH, Wooster R.

Genome Res. 2004 Feb;14(2):287-95.

3.

Detection of exonic copy-number changes using a highly efficient oligonucleotide-based comparative genomic hybridization-array method.

Saillour Y, Cossée M, Leturcq F, Vasson A, Beugnet C, Poirier K, Commere V, Sublemontier S, Viel M, Letourneur F, Barbot JC, Deburgrave N, Chelly J, Bienvenu T.

Hum Mutat. 2008 Sep;29(9):1083-90. doi: 10.1002/humu.20829.

PMID:
18683213
4.

High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.

Carr J, Bown NP, Case MC, Hall AG, Lunec J, Tweddle DA.

Cancer Genet Cytogenet. 2007 Jan 15;172(2):127-38.

PMID:
17213021
5.

Molecular characterization of breast cancer with high-resolution oligonucleotide comparative genomic hybridization array.

Andre F, Job B, Dessen P, Tordai A, Michiels S, Liedtke C, Richon C, Yan K, Wang B, Vassal G, Delaloge S, Hortobagyi GN, Symmans WF, Lazar V, Pusztai L.

Clin Cancer Res. 2009 Jan 15;15(2):441-51. doi: 10.1158/1078-0432.CCR-08-1791.

6.

MAPH: from gels to microarrays.

Patsalis PC, Kousoulidou L, Sismani C, Männik K, Kurg A.

Eur J Med Genet. 2005 Jul-Sep;48(3):241-9. Review.

PMID:
16179220
7.

Sequence-based, in situ detection of chromosomal abnormalities at high resolution.

Knoll JH, Rogan PK.

Am J Med Genet A. 2003 Sep 1;121A(3):245-57.

PMID:
12923866
8.

Construction of a high-density and high-resolution human chromosome X array for comparative genomic hybridization analysis.

Hayashi S, Honda S, Minaguchi M, Makita Y, Okamoto N, Kosaki R, Okuyama T, Imoto I, Mizutani S, Inazawa J.

J Hum Genet. 2007;52(5):397-405. Epub 2007 Apr 4.

PMID:
17406783
9.

High-resolution genomic profiles of breast cancer cell lines assessed by tiling BAC array comparative genomic hybridization.

Jönsson G, Staaf J, Olsson E, Heidenblad M, Vallon-Christersson J, Osoegawa K, de Jong P, Oredsson S, Ringnér M, Höglund M, Borg A.

Genes Chromosomes Cancer. 2007 Jun;46(6):543-58.

PMID:
17334996
10.

Design considerations for array CGH to oligonucleotide arrays.

Baldocchi RA, Glynne RJ, Chin K, Kowbel D, Collins C, Mack DH, Gray JW.

Cytometry A. 2005 Oct;67(2):129-36.

11.

Fine-mapping subtelomeric deletions and duplications by comparative genomic hybridization in 42 individuals.

DeScipio C, Spinner NB, Kaur M, Yaeger D, Conlin LK, Ambrosini A, Hu S, Shan S, Krantz ID, Riethman H.

Am J Med Genet A. 2008 Mar 15;146A(6):730-9. doi: 10.1002/ajmg.a.32216.

PMID:
18257100
12.

Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH.

Selzer RR, Richmond TA, Pofahl NJ, Green RD, Eis PS, Nair P, Brothman AR, Stallings RL.

Genes Chromosomes Cancer. 2005 Nov;44(3):305-19.

PMID:
16075461
13.
14.

Detection of submicroscopic constitutional chromosome aberrations in clinical diagnostics: a validation of the practical performance of different array platforms.

Zhang ZF, Ruivenkamp C, Staaf J, Zhu H, Barbaro M, Petillo D, Khoo SK, Borg A, Fan YS, Schoumans J.

Eur J Hum Genet. 2008 Jul;16(7):786-92. doi: 10.1038/ejhg.2008.14. Epub 2008 Feb 20.

15.

Array comparative genomic hybridization copy number profiling: a new tool for translational research in solid malignancies.

Costa JL, Meijer G, Ylstra B, Caldas C.

Semin Radiat Oncol. 2008 Apr;18(2):98-104. doi: 10.1016/j.semradonc.2007.10.005. Review.

PMID:
18314064
16.

Detection of small genomic imbalances using microarray-based multiplex amplifiable probe hybridization.

Patsalis PC, Kousoulidou L, Männik K, Sismani C, Zilina O, Parkel S, Puusepp H, Tõnisson N, Palta P, Remm M, Kurg A.

Eur J Hum Genet. 2007 Feb;15(2):162-72. Epub 2006 Nov 22.

17.

[Microarray-based comparative genomic hybridization in the study of constitutional chromosomal abnormalities].

Béri-Dexheimer M, Bonnet C, Chambon P, Brochet K, Grégoire MJ, Jonveaux P.

Pathol Biol (Paris). 2007 Feb;55(1):13-8. Epub 2006 May 11. Review. French.

PMID:
16697120
18.

Chromosomal anomalies on 6p25 in iris hypoplasia and Axenfeld-Rieger syndrome patients defined on a purpose-built genomic microarray.

Ekong R, Jeremiah S, Judah D, Lehmann O, Mirzayans F, Hung YC, Walter MA, Bhattacharya S, Gant TW, Povey S, Wolfe J.

Hum Mutat. 2004 Jul;24(1):76-85.

PMID:
15221791
19.
20.

Detection of known and novel genomic rearrangements by array based comparative genomic hybridisation: deletion of ZNF533 and duplication of CHARGE syndrome genes.

Monfort S, Roselló M, Orellana C, Oltra S, Blesa D, Kok K, Ferrer I, Cigudosa JC, Martínez F.

J Med Genet. 2008 Jul;45(7):432-7. doi: 10.1136/jmg.2008.057596. Epub 2008 Apr 15.

PMID:
18413373

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