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Background: Genomewide array comparative genomic hybridization (aCGH) has widely been utilized as the diagnostic tool in patients with non-syndromic intellectual disability (ID). Indeed, aCGH has identified pathogenic copy number variants (pCNVs), as well as variants of uncertain clinical significance (VsUS) and benign CNVs (bCNVs), in such patient... Read More»
Miki Asahina, Yusaku Endoh, Tomoko Matsubayashi, Koichi Hirano, Tokiko Fukuda and Tsutomu Ogata
Research Article: Neonat Pediatr Med 2016, 1:S1008
DOI:
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