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Phenylketonuria in Tunisian institutions for the mentally handicapped.
Khemir S, Tebib N, Nasrallah F, Ben Nour F, Mizouni H, Elasmi M, Sanhaji H, Jemaa R, Feki M, Ben Dridi MF, Mebazaa A, Kaabachi N. Khemir S, et al. Arch Dis Child. 2009 Aug;94(8):647-8. doi: 10.1136/adc.2008.143081. Arch Dis Child. 2009. PMID: 19628886 No abstract available.
A novel 22bp deletion in a Tunisian phenylketonuria family.
Khemir S, Siala H, Azzouz H, Tebib N, Dhondt JL, Messaoud T, Abdelhak S, Ben Dridi MF, Kaabachi N. Khemir S, et al. Pathol Biol (Paris). 2012 Dec;60(6):e87-9. doi: 10.1016/j.patbio.2012.03.007. Epub 2012 May 7. Pathol Biol (Paris). 2012. PMID: 22572109
[Molecular diagnosis of fragile X syndrome].
Ben Jemaa L, Khemir S, Maazoul F, Richard L, Beldjord C, Chaabouni M, Chaabouni H. Ben Jemaa L, et al. Among authors: khemir s. Tunis Med. 2008 Nov;86(11):973-7. Tunis Med. 2008. PMID: 19213487 French.