Genetic Disorders
| Image Thumbnail | Primary Image ID | Primary Image title | All taxonomy terms |
|---|---|---|---|
 |
LMP38898 | Bones, Hypophosphatasia | |
 |
LMP42947 | Skin, Steatocystoma | |
 |
LMP43224 | Breast, superficial myxoma | |
 |
LMP44206 | Bones, Robinow Syndrome | |
 |
LMP44357 | Bone Marrow, Gaucher’s disease | |
 |
LMP52459 | Bones, Robinow Syndrome | |
 |
LMP57268 | Body Morphology, Thanatophoric Dysplasia Type II | |
 |
LMP58951 | Bones, Robinow Syndrome | |
 |
LMP63244 | Liver, Alagille syndrome, CK7 stain | |
 |
LMP67318 | Bones, Robinow Syndrome |
