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Parsonage-Aldren-Turner Syndrome (MeSH) - C0221759 L0369767 S1671051 A1633010 M0328160 MeSH EN D020968 → |
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Parsonage-Turner Syndrome (MeSH) - C0221759 L0030595 S0071109 A0097983 M0328160 MeSH EP D020968 → |
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Part A, Medicare (MeSH) - C0079817 L0079817 S0071110 A0097984 M0024979 MeSH PM D016344 → |
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Part B, Medicare (MeSH) - C0079818 L0079818 S0071111 A0097985 M0024980 MeSH PM D016345 → |
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parthenin (MeSH) - C0070125 L0070125 S0190535 A0215171 M0077738 MeSH NM C022097 → |
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Parthenogeneses - C0030596 L0030596 S0071112 A0097986 M0015981 MeSH PM D010312 → |
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Parthenogenesis - C0030596 L0030596 S0071113 A0097989 M0015981 MeSH MH D010312 → |
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parthenolide (MeSH) - C0070126 L0070126 S0190536 A0215172 M0043371 MeSH NM C002669 → |
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Partial Albinism (MeSH) - C0080024 L0078919 S0071114 A0097990 M0024621 MeSH PM D016116 → |
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Partial Anencephalies (MeSH) - C0302356 L1402503 S1671687 A1633633 M0336992 MeSH PM D000757 → |
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