Additional file 6 of Loss-of-function maternal-effect mutations of PADI6 are associated with familial and sporadic Beckwith-Wiedemann syndrome with multi-locus imprinting disturbance
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https://springernature.figshare.com/articles/dataset/Additional_file_6_of_Loss-of-function_maternal-effect_mutations_of_PADI6_are_associated_with_familial_and_sporadic_Beckwith-Wiedemann_syndrome_with_multi-locus_imprinting_disturbance/12956050/1
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Additional file 6: Table S3. Maternal genetic variants in homozigosity or compound heterozigosity identified by WES.
补充材料6：表S3。通过全外显子组测序（Whole Exome Sequencing，WES）鉴定的呈现纯合性或复合杂合性的母体遗传变异。
提供机构：
figshare
创建时间：
2020-09-15
