Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
4 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
[McCune-Albright syndrome: a case report and literature review].
Pan Afr Med J. 2023 Sep 22;46:33. doi: 10.11604/pamj.2023.46.33.35274. eCollection 2023.
Pan Afr Med J. 2023.
PMID: 38145201
Free PMC article.
Review.
French.
A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.
Fendri-Kriaa N, Hsairi I, Kifagi C, Ellouze E, Mkaouar-Rebai E, Triki C, Fakhfakh F; Tunisian network on mental retardation study.
Fendri-Kriaa N, et al.
Biochem Biophys Res Commun. 2011 Jun 3;409(2):270-4. doi: 10.1016/j.bbrc.2011.04.140. Epub 2011 May 7.
Biochem Biophys Res Commun. 2011.
PMID: 21575601
Item in Clipboard
[Genetic factor of sex determination].
Abbas N, Toublanc J, Rappaport R, Fekete-Nihoul C, Boucekine C, Chabouni H, Fellous M.
Abbas N, et al. Among authors: chabouni h.
Bull Assoc Anat (Nancy). 1991 Mar;75(228):7-14.
Bull Assoc Anat (Nancy). 1991.
PMID: 1782471
Review.
French.
Item in Clipboard
[Autosomal recessive severe, proximal myopathy in children, common in Tunisia].
Ben Hamida M, Attia N, Chabouni H, Fardeau M.
Ben Hamida M, et al. Among authors: chabouni h.
Rev Neurol (Paris). 1983;139(4):289-97.
Rev Neurol (Paris). 1983.
PMID: 6612142
French.
Item in Clipboard
Cite
Cite