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The phenotype of recurrent 10q22q23 deletions and duplications.
Eur J Hum Genet. 2011 Apr;19(4):400-8. doi: 10.1038/ejhg.2010.211. Epub 2011 Jan 19.
Eur J Hum Genet. 2011.
PMID: 21248748
Free PMC article.
Mutation analysis of B3GALTL in Peters Plus syndrome.
Reis LM, Tyler RC, Abdul-Rahman O, Trapane P, Wallerstein R, Broome D, Hoffman J, Khan A, Paradiso C, Ron N, Bergner A, Semina EV.
Reis LM, et al. Among authors: broome d.
Am J Med Genet A. 2008 Oct 15;146A(20):2603-10. doi: 10.1002/ajmg.a.32498.
Am J Med Genet A. 2008.
PMID: 18798333
Free PMC article.
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