Additional file 3: 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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Non-recurrent pathogenic/likely pathogenic CNVs detected by array-CGH in 26 children with ID/DD, ASD and MCA. (XLSX 14 kb)
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Marketa Wayhelova创建时间：
2019-07-24
