M Chaâbouni

A novel <i>UBE3A</i> truncating mutation in large Tunisian Angelman syndrome pedigree

Leila Abaied, Médiha Trabelsi, M Chaâbouni et al. · American Journal of Medical Genetics Part A · 2009 · 77 citations

[Blepharitis due to Demodex: myth or reality?].

B. Kamoun, Meriem Fourati, M Mlik et al. · PubMed · 1999 · 48 citations

Incidence of mucopolysaccharidoses in Tunisia.

Ben Turkia H, Néji Tebib, Hatem Azzouz et al. · PubMed · 2009 · 42 citations

Clinical and genetic characterization of Bardet–Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis

O. M'hamdi, Claire Redin, Corinne Stoetzel et al. · Clinical Genetics · 2013 · 31 citations

Only two mutations detected in 15 Tunisian patients with 11β‐hydroxylase deficiency: the p.Q356X and the novel p.G379V

Maher Kharrat, Saoussen Trabelsi, M Chaâbouni et al. · Clinical Genetics · 2010 · 30 citations

Steroid 11β-Hydroxylase Deficiency, Genetics, Genetic Epidemiology +20