Marrow hyperplasia in skull and bone of a child with thalassemia,an inherited blood disease. In thalassemia the genetic defect,which could be either mutation or deletion,results in reduced rate of synthesis or no synthesis of one of the globin chains that make up hemoglobin | |
Licence : | Droits gérés |
Crédit: | Science Photo Library / Biophoto Associates |
Taille de l’image : | 4278 px × 2844 px |
Model Release : | Non requis |
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