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LMP67908 |
Brain, Alzheimer’s disease with presenilin 1 mutation |
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LMP68813 |
Heart, Leigh syndrome |
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LMP69657 |
Vulva, angiomyxoma |
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LMP72506 |
Eye, Granular corneal dystrophy |
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LMP72937 |
Skeleton, Thanatophoric Dysplasia Type II |
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LMP83004 |
Peripheral nerve, Amyloidosis |
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LMP85024 |
Bones, Robinow Syndrome |
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LMP87598 |
Soft palate, superficial myxoma |
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LMP88586 |
Ovotestis, Simpson-Golabi-Behmel Syndrome, calretinin stain |
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LMP91588 |
Skeletal Muscle, McArdle disease |
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