Large structural polymorphisms predispose genomic sequences to disease-causing rearrangements

Affiliations

Comment

S S Sanders. Clin Genet. 2011 Feb.

. 2011 Feb;79(2):134-5.

doi: 10.1111/j.1399-0004.2010.01587.x. Epub 2010 Nov 11.

¹ The Centre for Molecular Medicine and Therapeutics, 950 28th Avenue West, Vancouver, BC, V5Z 4H4, Canada. ssanders@cmmt.ubc.ca

No abstract available

Comment on

A large and complex structural polymorphism at 16p12.1 underlies microdeletion disease risk.
Antonacci F, Kidd JM, Marques-Bonet T, Teague B, Ventura M, Girirajan S, Alkan C, Campbell CD, Vives L, Malig M, Rosenfeld JA, Ballif BC, Shaffer LG, Graves TA, Wilson RK, Schwartz DC, Eichler EE. Antonacci F, et al. Nat Genet. 2010 Sep;42(9):745-50. doi: 10.1038/ng.643. Epub 2010 Aug 22. Nat Genet. 2010. PMID: 20729854 Free PMC article.