Particular Mal de Meleda Phenotypes in Tunisia and Mutations Founder Effect in the Mediterranean Region

Por Bchetnia, Mbarka, Laroussi, Nadia, Youssef, Monia, Charfeddine, Cherine, Ben Brick, Ahlem Sabrine, Boubaker, Mohamed Samir, Mokni, Mourad, Abdelhak, Sonia, Zili, Jameleddine, Benmously, Rym
Publicado em 2013

Identification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing

Por Laroussi, Nadia, Messaoud, Olfa, Chargui, Mariem, Ben Fayala, Chaima, Elahlafi, Abdelaziz, Mokni, Mourad, Bashamboo, Anu, McElreavey, Kenneth, Boubaker, Mohamed Samir, Yacoub Youssef, Houda, Abdelhak, Sonia
Publicado no Ann Dermatol (2017)

Further Evidence of Mutational Heterogeneity of the XPC Gene in Tunisian Families: A Spectrum of Private and Ethnic Specific Mutations

Por Ben Rekaya, Mariem, Jerbi, Manel, Messaoud, Olfa, Ben Brick, Ahlem Sabrine, Zghal, Mohamed, Mbarek, Chiraz, Chadli-Debbiche, Ashraf, Jones, Meriem, Mokni, Mourad, Boussen, Hamouda, Boubaker, Mohamed Samir, Fazaa, Becima, Yacoub-Youssef, Houda, Abdelhak, Sonia
Publicado em 2013

A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy

Por Ben Rekaya, Mariem, Laroussi, Nadia, Messaoud, Olfa, Jones, Mariem, Jerbi, Manel, Naouali, Chokri, Bouyacoub, Yosra, Chargui, Mariem, Kefi, Rym, Fazaa, Becima, Boubaker, Mohamed Samir, Boussen, Hamouda, Mokni, Mourad, Abdelhak, Sonia, Zghal, Mohamed, Khaled, Aida, Yacoub-Youssef, Houda
Publicado em 2014

Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases

Por Hamdi, Yosr, Boujemaa, Maroua, Ben Rekaya, Mariem, Ben Hamda, Cherif, Mighri, Najah, El Benna, Houda, Mejri, Nesrine, Labidi, Soumaya, Daoud, Nouha, Naouali, Chokri, Messaoud, Olfa, Chargui, Mariem, Ghedira, Kais, Boubaker, Mohamed Samir, Mrad, Ridha, Boussen, Hamouda, Abdelhak, Sonia
Publicado no J Transl Med (2018)