These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
144 related articles for article (PubMed ID: 21344636)
21. Integration of genomic copy number variations and chemotherapy-response biomarkers in pediatric sarcoma. Cheng L; Pandya PH; Liu E; Chandra P; Wang L; Murray ME; Carter J; Ferguson M; Saadatzadeh MR; Bijangi-Visheshsaraei K; Marshall M; Li L; Pollok KE; Renbarger JL BMC Med Genomics; 2019 Jan; 12(Suppl 1):23. PubMed ID: 30704460 [TBL] [Abstract][Full Text] [Related]
22. An Evolutionary Perspective on the Impact of Genomic Copy Number Variation on Human Health. Saitou M; Gokcumen O J Mol Evol; 2020 Jan; 88(1):104-119. PubMed ID: 31522275 [TBL] [Abstract][Full Text] [Related]
23. Copy number variations and stroke. Colaianni V; Mazzei R; Cavallaro S Neurol Sci; 2016 Dec; 37(12):1895-1904. PubMed ID: 27393281 [TBL] [Abstract][Full Text] [Related]
24. A high-resolution map of segmental DNA copy number variation in the mouse genome. Graubert TA; Cahan P; Edwin D; Selzer RR; Richmond TA; Eis PS; Shannon WD; Li X; McLeod HL; Cheverud JM; Ley TJ PLoS Genet; 2007 Jan; 3(1):e3. PubMed ID: 17206864 [TBL] [Abstract][Full Text] [Related]
25. Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in Taiwan. Lee CL; Lee CH; Chuang CK; Chiu HC; Chen YJ; Chou CL; Wu PS; Chen CP; Lin HY; Lin SP Pediatr Neonatol; 2019 Aug; 60(4):453-460. PubMed ID: 30581099 [TBL] [Abstract][Full Text] [Related]
26. Current analysis platforms and methods for detecting copy number variation. Li W; Olivier M Physiol Genomics; 2013 Jan; 45(1):1-16. PubMed ID: 23132758 [TBL] [Abstract][Full Text] [Related]
27. 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. PubMed ID: 19407672 [TBL] [Abstract][Full Text] [Related]
28. Copy number variants in pharmacogenetic genes. He Y; Hoskins JM; McLeod HL Trends Mol Med; 2011 May; 17(5):244-51. PubMed ID: 21388883 [TBL] [Abstract][Full Text] [Related]
29. Detection of copy number variation using SNP genotyping. Cooper GM; Mefford HC Methods Mol Biol; 2011; 767():243-52. PubMed ID: 21822880 [TBL] [Abstract][Full Text] [Related]
30. Comparative genomic hybridization to detect variation in the copy number of large DNA segments. Holcomb IN; Trask BJ Cold Spring Harb Protoc; 2011 Nov; 2011(11):1323-33. PubMed ID: 22046040 [TBL] [Abstract][Full Text] [Related]
35. Towards a comprehensive structural variation map of an individual human genome. Pang AW; MacDonald JR; Pinto D; Wei J; Rafiq MA; Conrad DF; Park H; Hurles ME; Lee C; Venter JC; Kirkness EF; Levy S; Feuk L; Scherer SW Genome Biol; 2010; 11(5):R52. PubMed ID: 20482838 [TBL] [Abstract][Full Text] [Related]
36. The characterisation of three types of genes that overlie copy number variable regions. Woodwark C; Bateman A PLoS One; 2011; 6(5):e14814. PubMed ID: 21637334 [TBL] [Abstract][Full Text] [Related]
37. An evolving view of copy number variants. Lauer S; Gresham D Curr Genet; 2019 Dec; 65(6):1287-1295. PubMed ID: 31076843 [TBL] [Abstract][Full Text] [Related]
38. Chromosome copy number variants in fetuses with syndromic malformations. Wang H; Chau MHK; Cao Y; Kwok KY; Choy KW Birth Defects Res; 2017 Jun; 109(10):725-733. PubMed ID: 28568742 [TBL] [Abstract][Full Text] [Related]
39. Inference of Causative Genes for Alzheimer's Disease Due to Dosage Imbalance. Sekine M; Makino T Mol Biol Evol; 2017 Sep; 34(9):2396-2407. PubMed ID: 28666362 [TBL] [Abstract][Full Text] [Related]
40. Copy number variation of individual cattle genomes using next-generation sequencing. Bickhart DM; Hou Y; Schroeder SG; Alkan C; Cardone MF; Matukumalli LK; Song J; Schnabel RD; Ventura M; Taylor JF; Garcia JF; Van Tassell CP; Sonstegard TS; Eichler EE; Liu GE Genome Res; 2012 Apr; 22(4):778-90. PubMed ID: 22300768 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]