Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

19 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
[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.
A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasia.
Ouertani I, Chaabouni M, Turki I, Lelorc'h M, Attié-Bitach T, Ben Jemaa L, Khouja-Gouider N, Chaabouni H. Ouertani I, et al. Eur J Med Genet. 2009 Jul-Aug;52(4):256-9. doi: 10.1016/j.ejmg.2009.01.004. Epub 2009 Feb 6. Eur J Med Genet. 2009. PMID: 19450439
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.
Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström syndromes.
Redin C, Le Gras S, Mhamdi O, Geoffroy V, Stoetzel C, Vincent MC, Chiurazzi P, Lacombe D, Ouertani I, Petit F, Till M, Verloes A, Jost B, Chaabouni HB, Dollfus H, Mandel JL, Muller J. Redin C, et al. Among authors: ouertani i. J Med Genet. 2012 Aug;49(8):502-12. doi: 10.1136/jmedgenet-2012-100875. Epub 2012 Jul 7. J Med Genet. 2012. PMID: 22773737 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
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
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
19 results