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	1.	An unusual three-way translocation t(21;8;1)(q22;q22;q32) in a case of acute myeloid leukemia (M2). [electronic resource] by Gmidène, Abir Sennana, Hlima Frikha, Rim Elloumi, Moez Belaaj, Hatem Saad, Ali Producer: 20120529 In: Annales de biologie clinique vol. 70 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	T(1;21;8)(p34;q22;q22): a novel variant of t(8;21) in acute myeloblastic leukemia with maturation. [electronic resource] by Gmidène, Abir Frikha, Rim Sennana, Hlima Elghezal, Hatem Elloumi, Moez Saad, Ali Producer: 20120822 In: Medical oncology (Northwood, London, England) vol. 28 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Cytogenetic profile of a large cohort of Tunisian de novo acute myeloid leukemia. [electronic resource] by Gmidène, Abir Sennana, Hlima Wahchi, Ines Youssef, Yosra Ben Jeddi, Ramzi Elloumi, Moez Saad, Ali Producer: 20120920 In: Hematology (Amsterdam, Netherlands) vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Trisomy and tetrasomy 15q11-q13 diagnosed by molecular cytogenetic analysis in two patients with mental retardation. [electronic resource] by Bouhjar, Inesse Ben Abdallah Gmidène, Abir Soyah, Najla Hanene, Hannachi Mougou, Soumaya Elghezal, Hatem Saad, Ali Producer: 20160914 In: Journal of pediatric genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Cytogenetic abnormalities in Tunisian de novo myelodysplastic syndrome: a comparison with other populations. [electronic resource] by Gmidène, Abir Sennana, Hlima Fenaux, Pierre Laatiri, Adnène Zarrouk, Mohamed Bouaziz, Houssem Harrabi, Imed Saad, Ali Producer: 20090109 In: Leukemia research vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	ETV6-RUNX1 Rearrangement in Tunisian Pediatric B-Lineage Acute Lymphoblastic Leukemia. [electronic resource] by Gmidène, Abir Elghezal, Hatem Sennana, Hlima Ben Youssef, Yosra Meddeb, Balkiss Elloumi, Moez Khlif, Abderrahim Saad, Ali Producer: 20110714 In: Advances in hematology vol. 2009 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Multiple myeloma following essential thrombocythemia. [electronic resource] by Ben Youssef, Yosra Gmidène, Abir Bouabid, Zahreddine Bouallegui, Sonia Sriha, Badreddine Zaier, Monia Sennana, Hlima Khelif, Abserrahim Producer: 20131105 In: Annales de biologie clinique vol. 71 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Cytogenetic analysis in a large series of children with non-syndromic mental retardation. [electronic resource] by Bouhjar, Inesse Ben Abdallah Gmidène, Abir Mougou-Zrelli, Soumaya Hannachi, Hanene Soyah, Najla Gadour, Naoufel Harrabi, Imed Elghezal, Hatem Saad, Ali Producer: 20160914 In: Journal of pediatric genetics vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Molecular cytogenetic and phenotypic characterization of ring chromosome 13 in three unrelated patients. [electronic resource] by Abdallah-Bouhjar, Inesse B Mougou-Zerelli, Soumaya Hannachi, Hanene Gmidène, Abir Labalme, Audrey Soyah, Najla Sanlaville, Damien Saad, Ali Elghezal, Hatem Producer: 20160914 In: Journal of pediatric genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Cytogenetic analysis of 298 newly diagnosed cases of acute lymphoblastic leukaemia in Tunisia. [electronic resource] by Gmidène, Abir Sennana, Hlima Elghezal, Hatem Ziraoui, Sihem Youssef, Yosra Ben Elloumi, Moez Issaoui, Lamia Harrabi, Imed Raynaud, Sophie Saad, Ali Producer: 20080729 In: Hematological oncology vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Array-CGH study of partial trisomy 9p without mental retardation. [electronic resource] by Bouhjar, Inesse Ben Abdallah Hannachi, Hanane Zerelli, Soumaya Mougou Labalme, Audrey Gmidène, Abir Soyah, Najla Missaoui, Sonia Sanlaville, Damien Elghezal, Hatem Saad, Ali Producer: 20111014 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Chromosomal microarray analysis of functional Xq27-qter disomy and deletion 3p26.3 in a boy with Prader-Willi like features and hypotonia. [electronic resource] by Ben-Abdallah-Bouhjar, Inesse Hannachi, Hanene Labalme, Audrey Gmidène, Abir Mougou, Soumaya Soyah, Najla Gribaa, Moez Sanlaville, Damien Elghezal, Hatem Saad, Ali Producer: 20121126 In: European journal of medical genetics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)