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Anémie de fanconi au CHU Hassan II Fès: à propos de 6 observations
Fanconi anemia is a recessive disorder associated with chromosomal instability. It is marked by phenotypical heterogeneity which includes medullary deficiency, a variable malformation syndrome, a predisposition to develop acute leukaemias myéloïdes (ALM) and a cellular over-sensitiveness with the ag...
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| Udgivet i: | Pan Afr Med J |
|---|---|
| Main Authors: | , , , , , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
The African Field Epidemiology Network
2017
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6011001/ https://ncbi.nlm.nih.gov/pubmed/29942418 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.11604/pamj.2017.28.286.4372 |
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