| 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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X Chromosome Inactivation - C0043297 L5313968 S6381299 A8434953 M0006765 MeSH MH D049951 → | Read definition... |
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X Chromosomes - C0043292 L0008636 S0100270 A0134363 M0023035 MeSH PM D014960 → | Read definition... |
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X Inactivation - C0043297 L1223694 S0100271 A8395581 M0006765 MeSH EP D049951 → | Read definition... |
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X Inactivations - C0043297 L1223694 S0100272 A8395582 M0006765 MeSH PM D049951 → | Read definition... |
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X Linked Adrenoleukodystrophy (MeSH) - C0162309 L1401874 S5912561 A6981193 M0000501 MeSH PM D000326 → | Read definition... |
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X Linked Hypohydridrotic Ectodermal Dysplasia (MeSH) - C0162359 L6102463 S7007145 A10911959 M0007033 MeSH PM D053358 → | Read definition... |
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X Linked Inheritance (MeSH) - C0241764 L1079536 S6371803 A8425457 M0473000 MeSH PM D050172 → | Read definition... |
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X Linked Retinoschisis (MeSH) - C0271091 L0591772 S2729126 A2375480 M0430675 MeSH PM D041441 → | Read definition... |
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X Protein, bcl-2-Associated (MeSH) - C0219474 L5549906 S6371807 A8425461 M0220651 MeSH PM D051028 → | Read definition... |
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X protein, hepatitis B (MeSH) - C0062529 L0148058 S0216512 A0238852 M0161128 MeSH CE C057628 → | Read definition... |
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