reference/6605871

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/6605871

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bibliographicCitation	Celestino-Soper PB, Shaw CA, Sanders SJ, Li J, Murtha MT, Ercan-Sencicek AG, Davis L, Thomson S, Gambin T, Chinault AC, Ou Z, German JR, Milosavljevic A, Sutcliffe JS, Cook EH, Stankiewicz P, State MW, Beaudet AL. Use of array CGH to detect exonic copy number variants throughout the genome in autism families detects a novel deletion in TMLHE. Hum Mol Genet. 2011 Nov 15;20(22):4360–70. PMID: 21865298; PMCID: PMC3196886.
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date	2011-08-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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language	English
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title	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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