BioMed Central | Articles which cite: Origins of chromosomal rearrangement hotspots in the human genome: evidence from the AZFa deletion hotspots.

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1.	Evidence for widespread reticulate evolution within human duplicons. Jackson MS, Oliver K, Loveland J, Humphray S, Dunham I, Rocchi M, Viggiano L, Park JP, Hurles ME, Santibanez-Koref M Am J Hum Genet 2005 Nov, 77:824-40 [PubMed Central] [PubMed] [Related articles]
2.	Traffic of genetic information between segmental duplications flanking the typical 22q11.2 deletion in velo-cardio-facial syndrome/DiGeorge syndrome. Pavlicek A, House R, Gentles AJ, Jurka J, Morrow BE Genome Res 2005 Nov, 15:1487-95 [PubMed Central] [PubMed] [Related articles]
3.	A chromosomal rearrangement hotspot can be identified from population genetic variation and is coincident with a hotspot for allelic recombination. Lindsay SJ, Khajavi M, Lupski JR, Hurles ME Am J Hum Genet 2006 Nov, 79:890-902 [PubMed Central] [PubMed] [Related articles]
4.	Low copy repeats mediate distal chromosome 22q11.2 deletions: sequence analysis predicts breakpoint mechanisms. Shaikh TH, O'Connor RJ, Pierpont ME, McGrath J, Hacker AM, Nimmakayalu M, Geiger E, Emanuel BS, Saitta SC Genome Res 2007 Apr, 17:482-91 [PubMed Central] [PubMed] [Related articles]
5.	A recurrent inversion on the eutherian X chromosome. Cáceres M, National Institutes of Health Intramural Sequencing Center Comparative Sequencing Program , Sullivan RT, Thomas JW Proc Natl Acad Sci U S A 2007 Nov 20, 104:18571-6 [PubMed Central] [PubMed] [Related articles]

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