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Spectrum of Genetic Diseases in Tunisia: Current Situation and Main Milestones Achieved.
Mezzi N, Messaoud O, Mkaouar R, Zitouna N, Romdhane S, Abdessalem G, Charfeddine C, Maazoul F, Ouerteni I, Hamdi Y, Zaouak A, Mrad R, Abdelhak S, Romdhane L. Mezzi N, et al. Among authors: maazoul f. Genes (Basel). 2021 Nov 19;12(11):1820. doi: 10.3390/genes12111820. Genes (Basel). 2021. PMID: 34828426 Free PMC article.
GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
Trabelsi M, Bahri W, Habibi M, Zainine R, Maazoul F, Ghazi B, Chaabouni H, Mrad R. Trabelsi M, et al. Among authors: maazoul f. Int J Pediatr Otorhinolaryngol. 2013 May;77(5):714-6. doi: 10.1016/j.ijporl.2013.01.024. Epub 2013 Feb 19. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23434199
[Epidemiologic and genetic study of trisomy 21 in Tunisia].
Chaabouni H, Smaoui N, Maazoul F, Ben Jemaa L, M'Rad R. Chaabouni H, et al. Among authors: maazoul f. Tunis Med. 1999 Aug-Sep;77(8-9):407-14. Tunis Med. 1999. PMID: 10611817 French. No abstract available.
3M syndrome: A Tunisian seven-cases series.
Khachnaoui-Zaafrane K, Ouertani I, Zanati A, Kandara H, Maazoul F, Mrad R. Khachnaoui-Zaafrane K, et al. Among authors: maazoul f. Eur J Med Genet. 2022 Mar;65(3):104448. doi: 10.1016/j.ejmg.2022.104448. Epub 2022 Feb 9. Eur J Med Genet. 2022. PMID: 35150935
Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patients.
Trabelsi M, Nouira M, Maazoul F, Kraoua L, Meddeb R, Ouertani I, Chelly I, Benoit V, Besbes G, Mrad R. Trabelsi M, et al. Among authors: maazoul f. Int J Pediatr Otorhinolaryngol. 2017 Dec;103:14-19. doi: 10.1016/j.ijporl.2017.09.029. Epub 2017 Sep 28. Int J Pediatr Otorhinolaryngol. 2017. PMID: 29224756
TOP3B: A Novel Candidate Gene in Juvenile Myoclonic Epilepsy?
Daghsni M, Lahbib S, Fradj M, Sayeb M, Kelmemi W, Kraoua L, Kchaou M, Maazoul F, Echebbi S, Ben Ali N, Abdelhak S, M'rad R. Daghsni M, et al. Among authors: maazoul f. Cytogenet Genome Res. 2018;154(1):1-5. doi: 10.1159/000486945. Epub 2018 Feb 28. Cytogenet Genome Res. 2018. PMID: 29490292
48 results