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
收藏Figshare2019-07-23 更新2026-04-29 收录
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https://figshare.com/articles/dataset/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/8989856
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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)
创建时间：
2019-07-23
