SD
Sarra Dimassi

Publications (8)

Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
Article scientifique · 2026
Autism in patients with Williams-Beuren syndrome: A re-evaluation of 31 Tunisian patients’ phenotype
Article scientifique · 2022
Clinical and molecular characterization of 1q43q44 deletion and corpus callosum malformations: 2 new cases and literature review
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
Neuronal migration genes and a familial translocation t(3;17): Candidate genes implicated in the phenotype
Article scientifique · 2019
Neuronal migration genes and a familial translocation t(3;17): Candidate genes implicated in the phenotype
Article scientifique · 2019
Neuronal migration genes and a familial translocation t(3;17): which genes are implicated in the phenotype?
Article scientifique · 2019
Clinical and molecular findings in nine new cases of tetrasomy 18p syndrome: FISH and array CGH characterization
Article scientifique · 2019

Domaines principaux

Sciences de la vie et biotechnologies6 Sciences de la santé2

Statistiques

Consultations14
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