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	1.	Transition m.3308T>C in the ND1 gene is associated with left ventricular hypertrabeculation/noncompaction. [electronic resource] by Zarrouk Mahjoub, Sinda Mehri, Sounira Ourda, Fatma Boussaada, Rafik Mechmeche, Rachid Arab, Saïda Ben Finsterer, Josef Producer: 20111207 In: Cardiology vol. 118 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy. [electronic resource] by Mahjoub, Sinda Sternberg, Damien Boussaada, Rafik Filaut, Sandrine Gmira, Fathi Mechmech, Rachid Jardel, Claude Arab, Saïda Ben Producer: 20080114 In: Diagnostic molecular pathology : the American journal of surgical pathology, part B vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Clinical and genetic analysis of two Tunisian otosclerosis families. [electronic resource] by Ali, Insaf Bel Hadj Thys, Melissa Beltaief, Najeh Schrauwen, Isabelle Dieltjens, Nele Vanderstraeten, Kathleen Besbes, Ghazi Mnif, Emna Hachicha, Slah Arab, Saïda Ben Camp, Guy Van Producer: 20070827 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus. [electronic resource] by Belguith, Hanen Aifa-Hmani, Mounira Dhouib, Houria Said, Mariem Ben Mosrati, Mohamed Ali Lahmar, Imed Moalla, Jihen Charfeddine, Ilhem Driss, Nabil Arab, Saida Ben Ghorbel, Abdelmonem Ayadi, Hammadi Masmoudi, Saber Producer: 20090615 In: Genetic testing and molecular biomarkers vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)