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VARIATION GENET - C0042333 L6331337 S7246483 A12076627 M0022526 MeSH DEV D014644 → |
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Variation, Antigen - C0003319 L0249325 S0097622 A0131484 M0001406 MeSH PM D000940 → |
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Variation, Antigen - C0003319 L0249325 S0097622 A0131484 M0001406 MeSH PM D000940 → |
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Variation, Antigenic - C0003319 L0003319 S0097623 A0131485 M0001406 MeSH EP D000940 → |
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Variation, Antigenic - C0003319 L0003319 S0097623 A0131485 M0001406 MeSH EP D000940 → |
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Variation, Clinical Practice - C0008970 L0008970 S0097624 A0131486 M0016794 MeSH EN D010818 → |
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Variation, Contingent Negative - C0009850 L0009850 S0097625 A0131487 M0005073 MeSH PM D003265 → |
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Variation, Inter-Observer - C0021713 L6196754 S0097626 A0131488 M0023931 MeSH PM D015588 → |
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Variation, Interobserver - C0021713 L0021713 S0097627 A0131489 M0023931 MeSH PM D015588 → |
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Variation, Intra-Observer - C0021861 L6196793 S0097628 A0131490 M0023932 MeSH PM D015588 → |
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