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Results: 10

1.

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
2.

A survey of analysis software for array-comparative genomic hybridisation studies to detect copy number variation.

Karimpour-Fard A, Dumas L, Phang T, Sikela JM, Hunter LE.

Hum Genomics. 2010 Aug;4(6):421-7. Review.

PMID:
20846932
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Zoom-in array comparative genomic hybridization (aCGH) to detect germline rearrangements in cancer susceptibility genes.

Staaf J, Borg A.

Methods Mol Biol. 2010;653:221-35. doi: 10.1007/978-1-60761-759-4_13. Review.

PMID:
20721746
[PubMed - indexed for MEDLINE]
4.

A three-step workflow procedure for the interpretation of array-based comparative genome hybridization results in patients with idiopathic mental retardation and congenital anomalies.

Poot M, Hochstenbach R.

Genet Med. 2010 Aug;12(8):478-85. doi: 10.1097/GIM.0b013e3181e3914a. Review.

PMID:
20734469
[PubMed - indexed for MEDLINE]
5.

[Current limitations and difficulties in application of microarray comparative genomic hybridization in prenatal diagnosis].

Chen Y, Choy KW.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011 Feb;28(1):47-51. doi: 10.3760/cma.j.issn.1003-9406.2011.01.011. Review. Chinese.

PMID:
21287509
[PubMed - indexed for MEDLINE]
6.

Interpretation of array comparative genome hybridization data: a major challenge.

Gijsbers AC, Schoumans J, Ruivenkamp CA.

Cytogenet Genome Res. 2011;135(3-4):222-7. doi: 10.1159/000334066. Epub 2011 Nov 12. Review.

PMID:
22086107
[PubMed - indexed for MEDLINE]
7.

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]
8.

Experimental designs for array comparative genomic hybridization technology.

McDonnell SK, Riska SM, Klee EW, Thorland EC, Kay NE, Thibodeau SN, Parker AS, Eckel-Passow JE.

Cytogenet Genome Res. 2013;139(4):250-7. doi: 10.1159/000348815. Epub 2013 Mar 27. Review.

PMID:
23548696
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

[Advanced molecular technologies for the diagnosis of congenital malformation in neonates].

Yang L, Wang HJ, Huang GY, Zhou WH.

Zhongguo Dang Dai Er Ke Za Zhi. 2013 Nov;15(11):960-4. Review. Chinese.

PMID:
24229588
[PubMed - indexed for MEDLINE]
Free Article
10.

Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns.

Coughlin CR 2nd, Scharer GH, Shaikh TH.

Genome Med. 2012 Oct 30;4(10):80. doi: 10.1186/gm381. eCollection 2012. Review.

PMID:
23114084
[PubMed]
Free PMC Article

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