DH
D. Hmida

Publications (5)

Molecular characterization of Porokeratosis in Tunisian patients with intraindividual and intrafamilial clinical heterogeneity
Article scientifique · 2023
Functional characterization of MLH1 missense variants unveils mechanisms of pathogenicity and clarifies role in cancer
Article scientifique · 2022
X-linked recessive ichthyosis in 8 Tunisian patients: awareness of misdiagnosis due to the technical trap of the STS pseudogene
Article scientifique · 2022
Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene
Article scientifique · 2021
Phenotypic Intrafamilial Variability Including H Syndrome and Rosai Dorfman Disease Associated With the Same c.1088G>A mutation in the SLC29A3 gene.
Article scientifique · 2021

Domaines principaux

Sciences de la vie et biotechnologies3 Sciences de la santé2

Statistiques

Consultations13
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