SM
Soumaya Mougou-Zerelli

Publications (10)

Clinical and genomic characterization of corpus callosum abnormalities (CCA) in 107 Tunisian patients using a stepwise diagnostic approach
Article scientifique · 2026
Case report: 7p22.3 deletion and 8q24.3 duplication in a patient with epilepsy and psychomotor delay—Does both possibly act to modulate a candidate gene region for the patient’s phenotype?
Article scientifique · 2023
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
Disorders of sex development in Wolf–Hirschhorn syndrome: a genotype–phenotype correlation and MSX1 as candidate gene
Article scientifique · 2021
Disorders of Sex Development in Wolf-Hirschhorn Syndrome: A Genotype-phenotype Correlation and MSX1 as Candidate Gene
Article scientifique · 2021
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 biotechnologies8 Sciences de la santé2

Statistiques

Consultations21
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