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	1.	[Association of Recklinghausen's disease, dental dystrophy and myopia in a Tunisian family]. [electronic resource] by Chaabouni, H M'Rad, R Younsi, C F Ferchiou, A Producer: 19881013 In: Journal de genetique humaine vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Epidemiologic and genetic study of trisomy 21 in Tunisia]. [electronic resource] by Chaabouni, H Smaoui, N Maazoul, F Ben Jemaa, L M'Rad, R Producer: 20000121 In: La Tunisie medicale vol. 77 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Myalgia in familial Mediterranean fever]. [electronic resource] by B'chir Hamzaoui, S Bouslama, K Abdallah, M M'rad, R M'rad, S Ben Dridi, M Producer: 20070629 In: Revue neurologique vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Y chromosome microdeletions in Tunisian infertile males. [electronic resource] by Rejeb, I M'rad, R Maazoul, F Trabelsi, M Ben Jemaa, L Chaabouni, M Zhioua, F Chaabouni, H Producer: 20080909 In: Pathologie-biologie vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Prevalence and incidence estimation of large NPHP1 homozygous deletion in Tunisian population. [electronic resource] by Chaari, I Trabelsi, M Goucha, R Elaribi, Y Kharrat, M Guarguah, T Maazoul, F Chaabouni, H M'rad, R Producer: 20130529 In: Pathologie-biologie vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A novel UBE3A truncating mutation in large Tunisian Angelman syndrome pedigree. [electronic resource] by Abaied, L Trabelsi, M Chaabouni, M Kharrat, M Kraoua, L M'rad, R Tebib, N Maazoul, F Chaabouni, H Producer: 20100405 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	[Junctional congenital bullous epidermolysis, cutaneous aplasia and pyloric atresia]. [electronic resource] by Cherif, A Cherif, F Siala-Guagi, F M'rad, R Raghi, H Boubaker, S Chaabouni, H Marrakchi, Z Boukef-Largueche, S Producer: 20050801 In: Annales de dermatologie et de venereologie vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndrome. [electronic resource] by Kraoua, L Chaabouni, M Trabelsi, M Chelly, I Maazoul, F Ben Abdallah, N Boukthir, S Barsaoui, S Chaabouni, H M'rad, R Producer: 20101005 In: Clinical genetics vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	[Genetic analysis of Turner syndrome: 89 cases in Tunisia]. [electronic resource] by Kammoun, I Chaabouni, M Trabelsi, M Ouertani, I Kraoua, L Chelly, I M'rad, R Ben Jemaa, L Maâzoul, F Chaabouni, H Producer: 20090224 In: Annales d'endocrinologie vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Linkage relationship between incontinentia pigmenti (IP2) and nine terminal X long arm markers. [electronic resource] by Sefiani, A M'rad, R Simard, L Vincent, A Julier, C Holvoet-Vermaut, L Heuertz, S Dahl, N Stalder, J F Peter, M O Producer: 19910402 In: Human genetics vol. 86 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosis. [electronic resource] by M'hamdi, O Redin, C Stoetzel, C Ouertani, I Chaabouni, M Maazoul, F M'rad, R Mandel, J L Dollfus, H Muller, J Chaabouni, H Producer: 20150330 In: Clinical genetics vol. 85 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379V. [electronic resource] by Kharrat, M Trabelsi, S Chaabouni, M Maazoul, F Kraoua, L Ben Jemaa, L Gandoura, N Barsaoui, S Morel, Y M'rad, R Chaabouni, H Producer: 20110308 In: Clinical genetics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Alport syndrome: a genetic study of 31 families. [electronic resource] by M'Rad, R Sanak, M Deschenes, G Zhou, J Bonaiti-Pellie, C Holvoet-Vermaut, L Heuertz, S Gubler, M C Broyer, M Grunfeld, J P Producer: 19930218 In: Human genetics vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	[Comparative respective importance of infrared analysis and classical chemical analysis in the etiologic diagnosis of urinary calculi]. [electronic resource] by Ben Ammar, S Fellah, H M'Rad, R Zghal, A Khiari, D Ayachu, F Abdelmoula, J Kammoun, A Lakhoua, R Daudon, M Mebazaa, A Belkahia, C Producer: 19990106 In: La Tunisie medicale vol. 76 Availability: No items available. Save to lists Add to cart (remove)
	15.	Prenatal diagnosis of chromosome disorders in Tunisian population. [electronic resource] by Chaabouni, H Chaabouni, M Maazoul, F M'Rad, R Jemaa, L B Smaoui, N Terras, K Kammoun, H Belghith, N Ridene, H Oueslati, B Zouari, F Producer: 20011204 In: Annales de genetique vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)