| Search & browse in old database A B C D E F G H I J K L M N O P Q R S T U V W X Y Z |
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GENET EPISTASIS - C0014589 L6332482 S7256373 A12083070 M0007597 MeSH DEV D004843 → |
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GENET HETEROGENEITY (MeSH) - C0242960 L6524482 S7595428 A12080863 M0028075 MeSH DEV D018740 → |
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GENET HUMAN - C0020124 L6332589 S7256374 A12083156 M0009145 MeSH DEV D005826 → |
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GENET HYPOSTASIS - C0014589 L6332595 S7256376 A12079444 M0007597 MeSH DEV D004843 → |
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GENET IDENTITY - C0017390 L6327281 S7256378 A12076219 M0016090 MeSH DEV D010375 → |
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GENET IMPRINTING (MeSH) - C0242614 L6518636 S7595429 A12088023 M0027618 MeSH DEV D018392 → |
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GENET INDUCTION - C0017391 L6329997 S7256379 A12083143 M0009066 MeSH DEV D005786 → |
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GENET INTERVENTION - C0017387 L6331744 S7256380 A12094004 M0009126 MeSH DEV D005818 → |
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GENET LINKAGE - C0023745 L6327384 S7595432 A12079747 M0012530 MeSH DEV D008040 → |
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GENET MARKER - C0017393 L6332746 S7256382 A12083151 M0009130 MeSH DEV D005819 → |
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