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Results: 1 to 20 of 100

1.

Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research.

Tabor HK, Cho MK.

Genet Med. 2007 Sep;9(9):626-31. Review.

PMID:
17873651
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Ethical and legal implications of whole genome and whole exome sequencing in African populations.

Wright GE, Koornhof PG, Adeyemo AA, Tiffin N.

BMC Med Ethics. 2013 May 28;14:21. doi: 10.1186/1472-6939-14-21.

PMID:
23714101
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

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
[PubMed - indexed for MEDLINE]
4.

Microdeletion and microduplication syndromes.

Vissers LE, Stankiewicz P.

Methods Mol Biol. 2012;838:29-75. doi: 10.1007/978-1-61779-507-7_2.

PMID:
22228006
[PubMed - indexed for MEDLINE]
5.

[Genomic abnormalities in children with mental retardation and autism: the use of comparative genomic hybridization in situ (HRCGH) and molecular karyotyping with DNA-microchips (array CGH)].

Vorsanova SG, Iurov IIu, Kurinnaia OS, Voinova VIu, Iurov IuB.

Zh Nevrol Psikhiatr Im S S Korsakova. 2013;113(8):46-9. Russian.

PMID:
24077551
[PubMed - indexed for MEDLINE]
6.

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.

Christian SL, Brune CW, Sudi J, Kumar RA, Liu S, Karamohamed S, Badner JA, Matsui S, Conroy J, McQuaid D, Gergel J, Hatchwell E, Gilliam TC, Gershon ES, Nowak NJ, Dobyns WB, Cook EH Jr.

Biol Psychiatry. 2008 Jun 15;63(12):1111-7. doi: 10.1016/j.biopsych.2008.01.009. Epub 2008 Mar 28.

PMID:
18374305
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Ethical aspects of participation in the database of genotypes and phenotypes of the National Center for Biotechnology Information: the Cancer and Leukemia Group B Experience.

Peppercorn J, Shapira I, Deshields T, Kroetz D, Friedman P, Spears P, Collyar DE, Shulman LN, Dressler L, Bertagnolli MM.

Cancer. 2012 Oct 15;118(20):5060-8. doi: 10.1002/cncr.27515. Epub 2012 Mar 13.

PMID:
22415847
[PubMed - indexed for MEDLINE]
Free Article
8.

Detecting copy number variation in the human genome using comparative genomic hybridization.

Tchinda J, Lee C.

Biotechniques. 2006 Oct;41(4):385, 387, 389 passim.

PMID:
17068952
[PubMed - indexed for MEDLINE]
Free Article
9.

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.

PMID:
16288307
[PubMed - indexed for MEDLINE]
Free Article
10.

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
[PubMed - indexed for MEDLINE]
11.

Comparative genomic hybridization.

Pinkel D, Albertson DG.

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

PMID:
16124865
[PubMed - indexed for MEDLINE]
12.

Comprehensive validation of array comparative genomic hybridization platforms: how much is enough?

Thorland EC, Gonzales PR, Gliem TJ, Wiktor AE, Ketterling RP.

Genet Med. 2007 Sep;9(9):632-41. Review.

PMID:
17873652
[PubMed - indexed for MEDLINE]
13.

Detection of DNA copy number alterations in cancer by array comparative genomic hybridization.

Michels E, De Preter K, Van Roy N, Speleman F.

Genet Med. 2007 Sep;9(9):574-84. Review.

PMID:
17873645
[PubMed - indexed for MEDLINE]
14.

Challenges in array comparative genomic hybridization for the analysis of cancer samples.

Nowak NJ, Miecznikowski J, Moore SR, Gaile D, Bobadilla D, Smith DD, Kernstine K, Forman SJ, Mhawech-Fauceglia P, Reid M, Stoler D, Loree T, Rigual N, Sullivan M, Weiss LM, Hicks D, Slovak ML.

Genet Med. 2007 Sep;9(9):585-95.

PMID:
17873646
[PubMed - indexed for MEDLINE]
15.

Copy number variations associated with idiopathic autism identified by whole-genome microarray-based comparative genomic hybridization.

Cho SC, Yim SH, Yoo HK, Kim MY, Jung GY, Shin GW, Kim BN, Hwang JW, Kang JJ, Kim TM, Chung YJ.

Psychiatr Genet. 2009 Aug;19(4):177-85. doi: 10.1097/YPG.0b013e32832bdafa.

PMID:
19407672
[PubMed - indexed for MEDLINE]
16.

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.

Lee C, Iafrate AJ, Brothman AR.

Nat Genet. 2007 Jul;39(7 Suppl):S48-54. Review.

PMID:
17597782
[PubMed - indexed for MEDLINE]
17.

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
18.

New challenges for informed consent through whole genome array testing.

Netzer C, Klein C, Kohlhase J, Kubisch C.

J Med Genet. 2009 Jul;46(7):495-6. doi: 10.1136/jmg.2009.068015. No abstract available.

PMID:
19571117
[PubMed - indexed for MEDLINE]
19.

SeeGH--a software tool for visualization of whole genome array comparative genomic hybridization data.

Chi B, DeLeeuw RJ, Coe BP, MacAulay C, Lam WL.

BMC Bioinformatics. 2004 Feb 9;5:13.

PMID:
15040819
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Array comparative genomic hybridisation of 52 subjects with a Smith-Magenis-like phenotype: identification of dosage sensitive loci also associated with schizophrenia, autism, and developmental delay.

Williams SR, Girirajan S, Tegay D, Nowak N, Hatchwell E, Elsea SH.

J Med Genet. 2010 Apr;47(4):223-9. doi: 10.1136/jmg.2009.068072. Epub 2009 Sep 14.

PMID:
19752160
[PubMed - indexed for MEDLINE]

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