Additional file 5: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
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CNVs of uncertain significance detected by array-CGH in 15 children with ID/DD, ASD and MCA (List 1), cnnLOH detected by CGHâ +â SNP microarrays in 8 children with ID/DD, ASD and MCA (List 2). (XLSX 17 kb)
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figshare创建时间：
2019-07-24
