High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia.
Nik-Zainal S, Strick R, Storer M, Huang N, Rad R, Willatt L, Fitzgerald T, Martin V, Sandford R, Carter NP, Janecke AR, Renner SP, Oppelt PG, Oppelt P, Schulze C, Brucker S, Hurles M, Beckmann MW, Strissel PL, Shaw-Smith C.
Nik-Zainal S, et al. Among authors: renner sp.
J Med Genet. 2011 Mar;48(3):197-204. doi: 10.1136/jmg.2010.082412. Epub 2011 Jan 28.
J Med Genet. 2011.
PMID: 21278390
Free PMC article.