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Page 1
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).
Essaddam L, Zitouni O, Kraoua L, Trabelsi M, Sassi H, Kmiha S, Charfi F, El Guiche D, Kebaïli R, Jaballah N, Rjeb M, Zouari N, El Aribi Y, Hizem S, Wannes S, Fkih Romdhane I, Sfar MT, Ben Hamouda H, Hadj Salem R, Khlayfia Z, Khmiss T, Monastiri K, Siala N, Chouchane S, Souaa H, Khochtali I, Mahjoub B, Sfar H, Ben Jemâa L, Abroug S, Boughamoura L, Kamoun I, Kamoun T, Mrad R, Ben Becher S. Essaddam L, et al. Among authors: ben jemaa l. J Pediatr Endocrinol Metab. 2023 Apr 21;36(6):577-583. doi: 10.1515/jpem-2022-0360. Print 2023 Jun 27. J Pediatr Endocrinol Metab. 2023. PMID: 37084413
[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: ben jemaa l. Tunis Med. 1999 Aug-Sep;77(8-9):407-14. Tunis Med. 1999. PMID: 10611817 French. No abstract available.
Y chromosome microdeletions in Tunisian infertile males.
Rejeb I, M'rad R, Maazoul F, Trabelsi M, Ben Jemaa L, Chaabouni M, Zhioua F, Chaabouni H. Rejeb I, et al. Among authors: ben jemaa l. Pathol Biol (Paris). 2008 May;56(3):111-5. doi: 10.1016/j.patbio.2007.05.002. Epub 2007 Nov 26. Pathol Biol (Paris). 2008. PMID: 18031951
[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: ben jemaa l. 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.
33 results