Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
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Shinawi M, et al. Among authors: graham bh.
J Med Genet. 2010 May;47(5):332-41. doi: 10.1136/jmg.2009.073015. Epub 2009 Nov 12.
J Med Genet. 2010.
PMID: 19914906
Free PMC article.