1. A New δ Chain Variant, Hb A2-Tunis [δ46(CD5)Gly → Glu; HBD: c.140G>A], Observed in a Tunisian Family in Association with a Compound Heterozygosity for Hb C [β6(A3)Glu → Lys; HBB: c.19G>A] β0-Thalassemia [IVS-I-1 (β143, G>A); HBB: c.92+1G>A]. (April 2014) Authors: Moumni, Imen; Zorai, Amine; Mahjoub, Sonia; Mosbahi, Ikbel; Chaouechi, Dorra; Benromdhane, Neila; Abbes, Salem Journal: Hemoglobin Issue: Volume 38:Number 2(2014) Page Start: 88 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Haplotype Map of Sickle Cell Anemia in Tunisia. (2nd July 2014) Authors: Moumni, Imen; Ben Mustapha, Maha; Sassi, Sarra; Zorai, Amine; Ben Mansour, Ikbel; Douzi, Kais; Chouachi, Dorra; Mellouli, Fethi; Bejaoui, Mohamed; Abbes, Salem Other Names: Lapaire Olav Academic Editor. Journal: Disease markers Issue: Volume 2014(2014) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Two new β+‐thalassemia mutation [β ‐56 (G → C); HBBc. −106 G → C] and [β −83 (G → A); HBBc. −133 G → A] described among the Tunisian population. Issue 5 (7th March 2015) Authors: Douzi, Kais; Moumni, Imen; Zorai, Amine; Ben Mustapha, Maha; Ben Mansour, Ikbel Mosbahi; Dorra, Chaouachi; Salem, Abbes Journal: American journal of human biology Issue: Volume 27:Issue 5(2015:Sep./Oct.) Page Start: 716 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗