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Additional file 4: 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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posted on 2019-07-24, 06:12 authored by Marketa Wayhelova, Jan Smetana, Vladimira Vallova, Eva Hladilkova, Hana Filkova, Marta Hanakova, Marcela Vilemova, Petra Nikolova, Barbora Gromesova, Renata Gaillyova, Petr Kuglik
Children’s patients with two pathogenic/likely pathogenic CNVs. (XLSX 11 kb)

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Masarykova Univerzita

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