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WDR73-related galloway mowat syndrome with collapsing glomerulopathy.
El Younsi M, Kraoua L, Meddeb R, Ferjani M, Trabelsi M, Ouertani I, Maazoul F, Abid N, Gargah T, M'rad R. El Younsi M, et al. Among authors: ouertani i. Eur J Med Genet. 2019 Sep;62(9):103550. doi: 10.1016/j.ejmg.2018.10.002. Epub 2018 Oct 10. Eur J Med Genet. 2019. PMID: 30315938
[Genetic analysis of Turner syndrome: 89 cases in Tunisia].
Kammoun I, Chaabouni M, Trabelsi M, Ouertani I, Kraoua L, Chelly I, M'rad R, Ben Jemaa L, Maâzoul F, Chaabouni H. Kammoun I, et al. Among authors: ouertani i. Ann Endocrinol (Paris). 2008 Nov;69(5):440-5. doi: 10.1016/j.ando.2008.01.007. Epub 2008 Jun 9. Ann Endocrinol (Paris). 2008. PMID: 18541220 French.
Prevalence of Bardet-Biedl syndrome in Tunisia.
M'hamdi O, Ouertani I, Maazoul F, Chaabouni-Bouhamed H. M'hamdi O, et al. Among authors: ouertani i. J Community Genet. 2011 Jun;2(2):97-9. doi: 10.1007/s12687-011-0040-6. Epub 2011 Feb 20. J Community Genet. 2011. PMID: 22109794 Free PMC article.
The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum.
Messaoud O, Ben Rekaya M, Jerbi M, Ouertani I, Kefi R, Laroussi N, Bouyacoub Y, Benfadhel S, Yacoub-Youssef H, Boubaker S, Zghal M, Mrad R, Amouri A, Abdelhak S. Messaoud O, et al. Among authors: ouertani i. Public Health Genomics. 2013;16(5):251-4. doi: 10.1159/000354584. Epub 2013 Sep 7. Public Health Genomics. 2013. PMID: 24021614
Perinatal-lethal Gaucher disease presenting as hydrops fetalis.
BenHamida E, Ayadi I, Ouertani I, Chammem M, Bezzine A, BenTmime R, Attia L, Mrad R, Marrakchi Z. BenHamida E, et al. Among authors: ouertani i. Pan Afr Med J. 2015 Jun 10;21:110. doi: 10.11604/pamj.2015.21.110.7052. eCollection 2015. Pan Afr Med J. 2015. PMID: 26327947 Free PMC article.
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: ouertani i. 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
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: ouertani i. 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
18 results