Additional file 5 of Novel genetic variants of KHDC3L and other members of the subcortical maternal complex associated with Beckwith–Wiedemann syndrome or Pseudohypoparathyroidism 1B and multi-locus imprinting disturbances
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https://springernature.figshare.com/articles/dataset/Additional_file_5_of_Novel_genetic_variants_of_KHDC3L_and_other_members_of_the_subcortical_maternal_complex_associated_with_Beckwith_Wiedemann_syndrome_or_Pseudohypoparathyroidism_1B_and_multi-locus_imprinting_disturbances/19919868/1
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Additional file 5: Table S3. List of the SNP genotypes of the whole chromosome 6 obtained by SNP- array analysis on mother and maternal grandparents of proband 1.
附加文件5：表S3。本列表收录了通过SNP芯片阵列（SNP-array）对先证者1的母亲及其外祖父母进行分析后，得到的6号全染色体单核苷酸多态性（Single Nucleotide Polymorphism，SNP）基因型列表。
提供机构：
Pereda, Arrate; Giaccari, Carlo; Prontera, Paolo; Accadia, Maria; Sparago, Angela; Monticelli, Maria; Pignata, Laura; Cerrato, Flavia; Hernandez Mora, Jose Ramon; Hay Mele, Bruno; Cecere, Francesco; Palumbo, Orazio; Carella, Massimo; Esteller, Manel; Acurzio, Basilia; Lapunzina, Pablo; Tenorio-Castano, Jair; Monteagudo-Sánchez, Ana; de Nanclares, Guiomar Perez; Monk, David; Cubellis, Maria Vittoria; Verma, Ankit; Riccio, Andrea; Piscopo, Carmelo
创建时间：
2022-05-30
