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Results: 1 to 20 of 90

1.

Array-based Identification of Copy Number Changes in a Diagnostic Setting: Simultaneous gene-focused and low resolution whole human genome analysis.

Marquis-Nicholson R, Doherty E, Love JM, Lan CC, George AM, Thrush A, Love DR.

Sultan Qaboos Univ Med J. 2013 Feb;13(1):69-79. Epub 2013 Feb 27.

PMID:
23573385
[PubMed]
Free PMC Article
2.

A Streamlined Protocol for Molecular Testing of the DMD Gene within a Diagnostic Laboratory: A Combination of Array Comparative Genomic Hybridization and Bidirectional Sequence Analysis.

Marquis-Nicholson R, Lai D, Lan CC, Love JM, Love DR.

ISRN Neurol. 2013;2013:908317. doi: 10.1155/2013/908317. Epub 2013 Feb 7.

PMID:
23476807
[PubMed]
Free PMC Article
3.

An oligonucleotide based array-CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation.

Toruner GA, Streck DL, Schwalb MN, Dermody JJ.

Am J Med Genet A. 2007 Apr 15;143A(8):824-9.

PMID:
17366576
[PubMed - indexed for MEDLINE]
4.

Genome-wide analysis of DNA copy-number changes using cDNA microarrays.

Pollack JR, Perou CM, Alizadeh AA, Eisen MB, Pergamenschikov A, Williams CF, Jeffrey SS, Botstein D, Brown PO.

Nat Genet. 1999 Sep;23(1):41-6.

PMID:
10471496
[PubMed - indexed for MEDLINE]
5.

Diagnosis of copy number variation by Illumina next generation sequencing is comparable in performance to oligonucleotide array comparative genomic hybridisation.

Hayes JL, Tzika A, Thygesen H, Berri S, Wood HM, Hewitt S, Pendlebury M, Coates A, Willoughby L, Watson CM, Rabbitts P, Roberts P, Taylor GR.

Genomics. 2013 Sep;102(3):174-81. doi: 10.1016/j.ygeno.2013.04.006. Epub 2013 Apr 15.

PMID:
23598253
[PubMed - indexed for MEDLINE]
6.

Comparative analysis of copy number detection by whole-genome BAC and oligonucleotide array CGH.

Neill NJ, Torchia BS, Bejjani BA, Shaffer LG, Ballif BC.

Mol Cytogenet. 2010 Jun 29;3:11. doi: 10.1186/1755-8166-3-11.

PMID:
20587050
[PubMed]
Free PMC Article
7.

Multiplex Amplifiable Probe Hybridization (MAPH) methodology as an alternative to comparative genomic hybridization (CGH).

Kousoulidou L, Sismani C, Patsalis PC.

Methods Mol Biol. 2010;653:47-71. doi: 10.1007/978-1-60761-759-4_4. Review.

PMID:
20721737
[PubMed - indexed for MEDLINE]
8.

Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform.

Aston E, Whitby H, Maxwell T, Glaus N, Cowley B, Lowry D, Zhu XL, Issa B, South ST, Brothman AR.

J Med Genet. 2008 May;45(5):268-74. doi: 10.1136/jmg.2007.055319. Epub 2008 Jan 4.

PMID:
18178633
[PubMed - indexed for MEDLINE]
9.

Identification of a duplication within the GDF9 gene and novel candidate genes for primary ovarian insufficiency (POI) by a customized high-resolution array comparative genomic hybridization platform.

Norling A, Hirschberg AL, Rodriguez-Wallberg KA, Iwarsson E, Wedell A, Barbaro M.

Hum Reprod. 2014 Aug;29(8):1818-27. doi: 10.1093/humrep/deu149. Epub 2014 Jun 17.

PMID:
24939957
[PubMed - in process]
Free PMC Article
10.

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.

PMID:
17311676
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

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
[PubMed - indexed for MEDLINE]
12.

Detection of clinically relevant exonic copy-number changes by array CGH.

Boone PM, Bacino CA, Shaw CA, Eng PA, Hixson PM, Pursley AN, Kang SH, Yang Y, Wiszniewska J, Nowakowska BA, del Gaudio D, Xia Z, Simpson-Patel G, Immken LL, Gibson JB, Tsai AC, Bowers JA, Reimschisel TE, Schaaf CP, Potocki L, Scaglia F, Gambin T, Sykulski M, Bartnik M, Derwinska K, Wisniowiecka-Kowalnik B, Lalani SR, Probst FJ, Bi W, Beaudet AL, Patel A, Lupski JR, Cheung SW, Stankiewicz P.

Hum Mutat. 2010 Dec;31(12):1326-42. doi: 10.1002/humu.21360. Epub 2010 Nov 2.

PMID:
20848651
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

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.

PMID:
17901113
[PubMed - indexed for MEDLINE]
Free Article
14.

Exon array CGH: detection of copy-number changes at the resolution of individual exons in the human genome.

Dhami P, Coffey AJ, Abbs S, Vermeesch JR, Dumanski JP, Woodward KJ, Andrews RM, Langford C, Vetrie D.

Am J Hum Genet. 2005 May;76(5):750-62. Epub 2005 Mar 8.

PMID:
15756638
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

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
[PubMed - indexed for MEDLINE]
16.

Custom oligonucleotide array-based CGH: a reliable diagnostic tool for detection of exonic copy-number changes in multiple targeted genes.

Vasson A, Leroux C, Orhant L, Boimard M, Toussaint A, Leroy C, Commere V, Ghiotti T, Deburgrave N, Saillour Y, Atlan I, Fouveaut C, Beldjord C, Valleix S, Leturcq F, Dodé C, Bienvenu T, Chelly J, Cossée M.

Eur J Hum Genet. 2013 Sep;21(9):977-87. doi: 10.1038/ejhg.2012.279. Epub 2013 Jan 23.

PMID:
23340513
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Designing a simple multiplex ligation-dependent probe amplification (MLPA) assay for rapid detection of copy number variants in the genome.

Shen Y, Wu BL.

J Genet Genomics. 2009 Apr;36(4):257-65. doi: 10.1016/S1673-8527(08)60113-7.

PMID:
19376486
[PubMed - indexed for MEDLINE]
18.

Integrated analysis of copy number alteration and RNA expression profiles of cancer using a high-resolution whole-genome oligonucleotide array.

Jung SH, Shin SH, Yim SH, Choi HS, Lee SH, Chung YJ.

Exp Mol Med. 2009 Jul 31;41(7):462-70. doi: 10.3858/emm.2009.41.7.051.

PMID:
19322034
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Utility of array CGH in molecular diagnosis of mitochondrial disorders.

Wang J, Rakhade M.

Methods Mol Biol. 2012;837:301-12. doi: 10.1007/978-1-61779-504-6_20.

PMID:
22215556
[PubMed - indexed for MEDLINE]
20.

Characterisation of hairy cell leukaemia by tiling resolution array-based comparative genome hybridisation: a series of 13 cases and review of the literature.

Nordgren A, Corcoran M, Sääf A, Bremer A, Kluin-Nelemans HC, Schoumans J, Grandér D.

Eur J Haematol. 2010 Jan 1;84(1):17-25. doi: 10.1111/j.1600-0609.2009.01334.x. Review.

PMID:
19682064
[PubMed - indexed for MEDLINE]

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