A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
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Girirajan S, et al. Among authors: siswara p.
Nat Genet. 2010 Mar;42(3):203-9. doi: 10.1038/ng.534. Epub 2010 Feb 14.
Nat Genet. 2010.
PMID: 20154674
Free PMC article.