1. A broad survey of DNA sequence data simulation tools. (23rd December 2019) Authors: Alosaimi, Shatha; Bandiang, Armand; van Biljon, Noelle; Awany, Denis; Thami, Prisca K; Tchamga, Milaine S S; Kiran, Anmol; Messaoud, Olfa; Hassan, Radia Ismaeel Mohammed; Mugo, Jacquiline; Ahmed, Azza; Bope, Christian D; Allali, Imane; Mazandu, Gaston K; Mulder, Nicola J; Chimusa, Emile R Journal: Briefings in functional genomics Issue: Volume 19:Number 1(2020) Page Start: 49 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A Founder Large Deletion Mutation in Xeroderma Pigmentosum-Variant Form in Tunisia: Implication for Molecular Diagnosis and Therapy. (3rd May 2014) Authors: 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 Other Names: Burmeister Margit Academic Editor. Journal: BioMed research international Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. 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. (25th April 2019) Authors: Sayeb, Marwa; Riahi, Zied; Laroussi, Nadia; Bonnet, Crystel; Romdhane, Lilia; Mkaouar, Rahma; Zaouak, Anissa; Marrakchi, Jihene; Abdessalem, Ghaith; Messaoud, Olfa; Bouchniba, Oussema; Ghilane, Nacer; Mokni, Mourad; Besbes, Ghazi; Yacoub‐Youssef, Houda; Petit, Christine; Abdelhak, Sonia Journal: International journal of dermatology Issue: Volume 58:Number 12(2019) Page Start: 1439 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Congenital lamellar ichthyosis in Tunisia associated with vitamin D rickets caused by a founder nonsense mutation in the TGM1 gene. (10th April 2019) Authors: Zaouak, Anissa; Abdessalem, Ghaith; Mkaouar, Rahma; Messaoud, Olfa; Abdelhak, Sonia; Hammami, Houda; Fenniche, Samy Journal: International journal of dermatology Issue: Volume 58:Number 7(2019) Page Start: e135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Cytogenetic and molecular diagnosis of Fanconi anemia revealed two hidden phenotypes: Disorder of sex development and cerebro‐oculo‐facio‐skeletal syndrome. Issue 7 (23rd May 2019) Authors: Ben Haj Ali, Abir; Amouri, Ahlem; Sayeb, Marwa; Makni, Saloua; Hammami, Wajih; Naouali, Chokri; Dallali, Hamza; Romdhane, Lilia; Bashamboo, Anu; McElreavey, Kenneth; Abdelhak, Sonia; Messaoud, Olfa Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 7(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia. Issue 2 (16th July 2015) Authors: Ben Halim, Nizar; Hsouna, Sana; Lasram, Khaled; Rejeb, Insaf; Walha, Asma; Talmoudi, Faten; Messai, Habib; Sabrine Ben Brick, Ahlem; Ouragini, Houyem; Cherif, Wafa; Nagara, Majdi; Rhouma, Faten Ben; Chouchene, Ibtissem; Ouechtati, Farah; Bouyacoub, Yosra; Ben Rekaya, Mariem; Messaoud, Olfa; Ben A... Journal: American journal of human biology Issue: Volume 28:Issue 2(2016:Mar./Apr.) Page Start: 171 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Epidemiological trends and clinicopathological features of cutaneous melanoma in sporadic and xeroderma pigmentosum Tunisian patients. (26th October 2016) Authors: Naouali, Chokri; Jones, Meriem; Nabouli, Imen; Jerbi, Manel; Tounsi, Haifa; Ben Rekaya, Mariem; Ben Ahmed, Melika; Bouhaouala, Balkiss; Messaoud, Olfa; Khaled, Aida; Zghal, Mohamed; Abdelhak, Sonia; Boubaker, Samir; Yacoub‐Youssef, Houda Journal: International journal of dermatology Issue: Volume 56:Number 1(2017) Page Start: 40 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Further Evidence of Mutational Heterogeneity of the XPC Gene in Tunisian Families: A Spectrum of Private and Ethnic Specific Mutations. (25th July 2013) Authors: 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 Other Names: Bernstein Sanford I. Academic Editor. Journal: BioMed research international Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. H syndrome: Clinical, histological and genetic investigation in Tunisian patients. Issue 8 (29th May 2018) Authors: Jaouadi, Hager; Zaouak, Anissa; Sellami, Khadija; Messaoud, Olfa; Chargui, Mariem; Hammami, Houda; Jones, Meriem; Jouini, Raja; Chadli Debbiche, Achraf; Chraiet, Karima; Fenniche, Sami; Mrad, Ridha; Mokni, Mourad; Turki, Hamida; Benkhalifa, Rym; Abdelhak, Sonia Journal: Journal of dermatology Issue: Volume 45:Issue 8(2018) Page Start: 978 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. High frequency of exon 15 deletion in the FANCA gene in Tunisian patients affected with Fanconi anemia disease: implication for diagnosis. Issue 2 (5th February 2014) Authors: Amouri, Ahlem; Talmoudi, Faten; Messaoud, Olfa; d'Enghien, Catherine D.; Rekaya, Mariem B.; Allegui, Ines; Azaiez, Héla; Kefi, Rym; Abdelhak, Ahlem; Meseddi, Sondes H.; Torjemane, Lamia; Ouederni, Monia; Mellouli, Fethi; Abid, Héla B.; Aissaoui, Lamia; Bejaoui, Mohamed; Othmen, Tarek B.; Lyonnet,... Journal: Molecular genetics & genomic medicine Issue: Volume 2:Issue 2(2014:Mar.) Page Start: 160 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗