Dorra H'Mida
2PUBLICATIONS
5CO-AUTHORS

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Publications (2)
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|Oct 18, 2021
Phenotypic intrafamilial variability including H syndrome and Rosai-Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene.Hamza Chouk, Mohamed Ben Rejeb, Lobna Boussofara
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