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Supplement: 439_2024_2691_MOESM2_ESM.xlsx › MSH2
Analysis of clinically relevant variants from ancestrally diverse Asian genomes.
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36335097 (PubMed )
Supplement: 41467_2022_34116_MOESM4_ESM.zip › NCOMMS-22-14716A_SupplementaryData › NCOMM-22-14716A_SupplementaryData_5.xlsx › SuppData_5
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