Publications by authors named "Marwa Sayeb"

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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Marwa Sayeb

Front Genet· June 2024

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Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, Marwa Sayeb

Front Genet· April 2024

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A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.
Marwa Sayeb, Zied Riahi, Nadia Laroussi, Crystel Bonnet, Lilia Romdhane

Int J Dermatol· December 2019

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Granular type I corneal dystrophy in a large consanguineous Tunisian family with homozygous p.R124S mutation in the gene.
Yosra Bouyacoub, Yousra Falfoul, Mariem Ouederni, Marwa Sayeb, Aschraf Chedli

Ophthalmic Genet· August 2019

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Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro-oculo-facio-skeletal syndrome.
Abir Ben Haj Ali, Ahlem Amouri, Marwa Sayeb, Saloua Makni, Wajih Hammami

Mol Genet Genomic Med· July 2019

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TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?
Marwa Daghsni, Saida Lahbib, Mohamed Fradj, Marwa Sayeb, Wided Kelmemi

Cytogenet Genome Res· April 2018

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