Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomas-Reference-Cited by-同舟云学术

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Rates of loss of heterozygosity and mitotic recombination in NF2 schwannomas, sporadic vestibular schwannomas and schwannomatosis schwannomas

Published:2010-08-23 Issue:47 Volume:29 Page:6216-6221
ISSN:0950-9232
Container-title:Oncogene
language:en
Short-container-title:Oncogene

Author:

Hadfield K D,Smith M J,Urquhart J E,Wallace A J,Bowers N L,King A T,Rutherford S A,Trump D,Newman W G,Evans D G

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Molecular Biology

Link

http://www.nature.com/articles/onc2010363.pdf

Reference17 articles.

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2. Carbone L, Harris RA, Vessere GM, Mootnick AR, Humphray S, Rogers J et al. (2009). Evolutionary breakpoints in the gibbon suggest association between cytosine methylation and karyotype evolution. PLoS Genet 5: e1000538.

3. De Raedt T, Maertens O, Chmara M, Brems H, Heyns I, Sciot R et al. (2006). Somatic loss of wild type NF1 allele in neurofibromas: Comparison of NF1 microdeletion and non-microdeletion patients. Genes Chromosomes Cancer 45: 893–904.

4. Dunham I, Shimizu N, Roe BA, Chissoe S, Hunt AR, Collins JE et al. (1999). The DNA sequence of human chromosome 22. Nature 402: 489–495.

5. Edelmann L, Pandita RK, Morrow BE . (1999). Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome. Am J Hum Genet 64: 1076–1086.

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