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Items: 1 to 20 of 63

1.

The use of arrays to detect copy-number variations in clinical practice.

Sikkema-Raddatz B, Sijmons RH.

Hum Mutat. 2012 Jun;33(6):905. doi: 10.1002/humu.22084. No abstract available.

PMID:
22570302
2.

Oligonucleotide microarrays in constitutional genetic diagnosis.

Keren B, Le Caignec C.

Expert Rev Mol Diagn. 2011 Jun;11(5):521-32. doi: 10.1586/ERM.11.32. Review.

PMID:
21707460
3.

Bioinformatics for copy number variation data.

Warden M, Pique-Regi R, Ortega A, Asgharzadeh S.

Methods Mol Biol. 2011;719:235-49. doi: 10.1007/978-1-61779-027-0_11.

PMID:
21370087
4.

Detection of copy number changes at the NF1 locus with improved high-resolution array CGH.

Shen MH, Mantripragada K, Dumanski JP, Frayling I, Upadhyaya M.

Clin Genet. 2007 Sep;72(3):238-44.

PMID:
17718862
5.

Exploiting sequence similarity to validate the sensitivity of SNP arrays in detecting fine-scaled copy number variations.

Wong G, Leckie C, Gorringe KL, Haviv I, Campbell IG, Kowalczyk A.

Bioinformatics. 2010 Apr 15;26(8):1007-14. doi: 10.1093/bioinformatics/btq088. Epub 2010 Feb 25.

PMID:
20189937
6.

Evaluation of oligonucleotide sequence capture arrays and comparison of next-generation sequencing platforms for use in molecular diagnostics.

Hoppman-Chaney N, Peterson LM, Klee EW, Middha S, Courteau LK, Ferber MJ.

Clin Chem. 2010 Aug;56(8):1297-306. doi: 10.1373/clinchem.2010.145441. Epub 2010 Jun 18. Erratum in: Clin Chem. 2011 Jan;57(1):141.

7.

Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.

Shen Y, Irons M, Miller DT, Cheung SW, Lip V, Sheng X, Tomaszewicz K, Shao H, Fang H, Tang HS, Irons M, Walsh CA, Platt O, Gusella JF, Wu BL.

Clin Chem. 2007 Dec;53(12):2051-9. Epub 2007 Sep 27.

9.

Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors.

Dougherty MJ, Tooke LS, Sullivan LM, Hakonarson H, Wainwright LM, Biegel JA.

Cancer Genet. 2012 Jan-Feb;205(1-2):42-54. doi: 10.1016/j.cancergen.2012.01.014.

PMID:
22429597
10.

Detection of chromosomal abnormalities using high resolution arrays in clinical cancer research.

Dalmasso C, Broët P.

J Biomed Inform. 2011 Dec;44(6):936-42. doi: 10.1016/j.jbi.2011.06.003. Epub 2011 Jun 15.

11.

[Array-CGH for routine diagnosis of cryptic chromosomal imbalances].

Andrieux J.

Pathol Biol (Paris). 2008 Sep;56(6):368-74. doi: 10.1016/j.patbio.2008.04.011. Epub 2008 Jun 2. Review. French.

PMID:
18514435
12.

High-resolution copy number array in the molecular cytogenetic diagnostics of pediatric malignant hematological disorders.

Wikhager C, Ögärd I, Martinsson T, Abrahamsson J, Palmqvist L, Sjögren H.

Oncol Rep. 2012 May;27(5):1429-34. doi: 10.3892/or.2012.1689. Epub 2012 Feb 16.

PMID:
22344473
13.

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
14.
15.

A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosis.

Wang H, Wang L, Ma M, Song Z, Zhang J, Xu G, Fan J, Li N, Cram DS, Yao Y.

J Genet Genomics. 2014 Aug 20;41(8):453-6. doi: 10.1016/j.jgg.2014.06.007. Epub 2014 Jul 17. No abstract available.

PMID:
25160978
16.

High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical setting.

Wincent J, Anderlid BM, Lagerberg M, Nordenskjöld M, Schoumans J.

Clin Genet. 2011 Feb;79(2):147-57. doi: 10.1111/j.1399-0004.2010.01442.x.

PMID:
20486943
17.

Evaluation of the efficacy of constitutional array-based comparative genomic hybridization in the diagnosis of aneuploidy using genomic and amplified DNA.

Tan NH, Palmer R, Wang R.

J Obstet Gynaecol Res. 2010 Feb;36(1):19-26. doi: 10.1111/j.1447-0756.2009.01110.x.

PMID:
20178523
18.

SNP array analysis in constitutional and cancer genome diagnostics--copy number variants, genotyping and quality control.

de Leeuw N, Hehir-Kwa JY, Simons A, Geurts van Kessel A, Smeets DF, Faas BH, Pfundt R.

Cytogenet Genome Res. 2011;135(3-4):212-21. doi: 10.1159/000331273. Epub 2011 Sep 16. Review.

PMID:
21934286
19.

Microarray-based genomic DNA profiling technologies in clinical molecular diagnostics.

Shen Y, Wu BL.

Clin Chem. 2009 Apr;55(4):659-69. doi: 10.1373/clinchem.2008.112821. Epub 2009 Feb 20. Review.

20.

Preprocessing and downstream analysis of microarray DNA copy number profiles.

van de Wiel MA, Picard F, van Wieringen WN, Ylstra B.

Brief Bioinform. 2011 Jan;12(1):10-21. doi: 10.1093/bib/bbq004. Epub 2010 Feb 19. Review.

PMID:
20172948

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