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Additional file 3: Table S2. of Comprehensive whole genome sequence analyses yields novel genetic and structural insights for Intellectual Disability

Year: 2017

Type: dataset

Abstract: Primers for verification - All primer sequences used for SNV, CNV and SV verification. (XLSX 18 kb)

Source: Figshare

DOI: 10.6084/m9.figshare.c.3787337_d4

Authors: Zahir, Farah, Mwenifumbo, Jill, Chun, Hye-Jung, Lim, Emilia, Karnebeek, Clara Van, Couse, Madeline, Mungall, Karen, Lee, Leora, Makela, Nancy, Linlea Armstrong, Boerkoel, Cornelius, Langlois, Sylvie, McGillivray, Barbara, Jones, Steven, Friedman, Jan, Marra, Marco

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

Open Access status: green

OpenAlex ID: W4394425901

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