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Items: 1 to 20 of 360

1.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.

BMC Genomics. 2007 Feb 20;8:53.

2.

Progress in concurrent analysis of loss of heterozygosity and comparative genomic hybridization utilizing high density single nucleotide polymorphism arrays.

Zhou X, Rao NP, Cole SW, Mok SC, Chen Z, Wong DT.

Cancer Genet Cytogenet. 2005 May;159(1):53-7. Review.

PMID:
15860358
3.

Recent advances in array comparative genomic hybridization technologies and their applications in human genetics.

Lockwood WW, Chari R, Chi B, Lam WL.

Eur J Hum Genet. 2006 Feb;14(2):139-48. Review.

4.

[Analysis of genomic copy number alterations of malignant lymphomas and its application for diagnosis].

Tagawa H.

Gan To Kagaku Ryoho. 2007 Jul;34(7):975-82. Review. Japanese.

PMID:
17637530
5.

Single nucleotide polymorphism array analysis of cancer.

Dutt A, Beroukhim R.

Curr Opin Oncol. 2007 Jan;19(1):43-9. Review.

PMID:
17133111
6.

Microarray-based comparative genomic hybridization and its applications in human genetics.

Oostlander AE, Meijer GA, Ylstra B.

Clin Genet. 2004 Dec;66(6):488-95. Review.

PMID:
15521975
8.

Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors.

Kallioniemi OP, Kallioniemi A, Piper J, Isola J, Waldman FM, Gray JW, Pinkel D.

Genes Chromosomes Cancer. 1994 Aug;10(4):231-43. Review.

PMID:
7522536
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11.

[Genomic profiling: from molecular cytogenetics to DNA arrays].

Theillet C, Orsetti B, Redon R, Manoir SD.

Bull Cancer. 2001 Mar;88(3):261-8. Review. French.

12.

Application of array-based whole genome scanning technologies as a cytogenetic tool in haematological malignancies.

Maciejewski JP, Tiu RV, O'Keefe C.

Br J Haematol. 2009 Sep;146(5):479-88. doi: 10.1111/j.1365-2141.2009.07757.x. Epub 2009 Jun 26. Review.

PMID:
19563474
13.

[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
14.

Computational methods for identification of recurrent copy number alteration patterns by array CGH.

Shah SP.

Cytogenet Genome Res. 2008;123(1-4):343-51. doi: 10.1159/000184726. Epub 2009 Mar 11. Review.

PMID:
19287173
15.

Array-based comparative genomic hybridization in clinical diagnosis.

Bejjani BA, Theisen AP, Ballif BC, Shaffer LG.

Expert Rev Mol Diagn. 2005 May;5(3):421-9. Review.

PMID:
15934818
16.

Comparative genomic hybridization.

Pinkel D, Albertson DG.

Annu Rev Genomics Hum Genet. 2005;6:331-54. Review.

PMID:
16124865
17.

[Advances in high-density whole genome-wide single nucleotide polymorphism array in cancer research].

Zeng ZY, Xiong W, Zhou YH, Li XL, Li GY.

Ai Zheng. 2006 Nov;25(11):1454-8. Review. Chinese.

PMID:
17094921
18.
19.

Detection of chromosomal abnormalities by comparative genomic hybridization.

Lapierre JM, Tachdjian G.

Curr Opin Obstet Gynecol. 2005 Apr;17(2):171-7. Review.

PMID:
15758611
20.

BAC to the future! or oligonucleotides: a perspective for micro array comparative genomic hybridization (array CGH).

Ylstra B, van den Ijssel P, Carvalho B, Brakenhoff RH, Meijer GA.

Nucleic Acids Res. 2006 Jan 26;34(2):445-50. Print 2006. Review.

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