Germline rates of de novo meiotic deletions and duplications causing several genomic disorders-Reference-Cited by-同舟云学术

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Germline rates of de novo meiotic deletions and duplications causing several genomic disorders

Published:2007-12-02 Issue:1 Volume:40 Page:90-95
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Turner Daniel J,Miretti Marcos,Rajan Diana,Fiegler Heike,Carter Nigel P,Blayney Martyn L,Beck Stephan,Hurles Matthew E

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng.2007.40.pdf

Reference32 articles.

1. Stankiewicz, P. & Lupski, J.R. Genome architecture, rearrangements and genomic disorders. Trends Genet. 18, 74–82 (2002).

2. Lupski, J.R. & Stankiewicz, P. Genomic disorders: molecular mechanisms for rearrangements and conveyed phenotypes. PLoS Genet. 1, e49 (2005).

3. Redon, R. et al. Global variation in copy number in the human genome. Nature 444, 444–454 (2006).

4. Hurles, M.E. & Lupski, J.R. Recombination hotspots in nonallelic homologous recombination. in Genomic Disorders: the Genomic Basis of Disease Ch. 24 (eds. Lupski, J.R. & Stankiewicz, P.) 341–355 (Humana Press, Totowa, New Jersey, USA, 2006).

5. Chance, P.F. et al. Two autosomal-dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome-17. Hum. Mol. Genet. 3, 223–228 (1994).

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