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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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.
创建时间：
2022-05-28
