Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE.
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Celestino-Soper PB, et al. Among authors: shaw ca.
Hum Mol Genet. 2011 Nov 15;20(22):4360-70. doi: 10.1093/hmg/ddr363. Epub 2011 Aug 24.
Hum Mol Genet. 2011.
PMID: 21865298
Free PMC article.