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	1.	X linked mental retardation. [electronic resource] by Rejeb, Imen Ben Jemaa, Lamia Chaabouni, Habiba Producer: 20100106 In: La Tunisie medicale vol. 87 Availability: No items available. Save to lists Add to cart (remove)
	2.	Allele frequency distribution of the D1S80 VNTR locus in a Tunisian population. [electronic resource] by Kallel, Faouzi Mrad, Ridha Refai, Mohamed Chaabouni, Myriam Chaabouni, Habiba Producer: 20051206 In: Journal of forensic sciences vol. 50 Availability: No items available. Save to lists Add to cart (remove)
	3.	Subtelomeric microduplications in three sisters with moderate mental retardation. [electronic resource] by Hila, Lamia Tébourbi, Hedia Abeid, Leila Rejeb, Imen Chaabouni, Habiba Producer: 20110321 In: Biochemical genetics vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Detection of a frequent duplicated CYP21A2 gene carrying a Q318X mutation in a general population with quantitative PCR methods. [electronic resource] by Kharrat, Maher Riahi, Awatef Maazoul, Faouzi M'rad, Ridha Chaabouni, Habiba Producer: 20110822 In: Diagnostic molecular pathology : the American journal of surgical pathology, part B vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Interest of studying subtelomeric abnormalities by in situ fluorescent hybridization to explore idiopathic mental retardation]. [electronic resource] by Hila, Lamia Ben Jemaa, Lamia Daoudi, Raja Maazoul, Faouzi Chaabouni, Habiba Producer: 20090623 In: La Tunisie medicale vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	6.	Autism: an overview of genetic aetiology. [electronic resource] by Bayou, Nadia M'rad, Ridha Ahlem, B Béchir Helayem, Mohamed Chaabouni, Habiba Producer: 20090313 In: La Tunisie medicale vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	7.	A novel 13-bp deletion in exon 1 of CYP21 gene causing severe congenital adrenal hyperplasia. [electronic resource] by Kharrat, Maher Tardy, Véronique M'rad, Ridha Maazoul, Faouzi Morel, Yves Chaabouni, Habiba Producer: 20060203 In: Diagnostic molecular pathology : the American journal of surgical pathology, part B vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	[Genetics of inflammatory bowel disease]. [electronic resource] by Zouiten, Mekki Lilia Khalfaoui, Taoufik Boubaker, Jalel Chaabouni, Habiba Filali, Azza Mechmeche, Rachid Producer: 20050222 In: La Tunisie medicale vol. 82 Availability: No items available. Save to lists Add to cart (remove)
	9.	MLPA subtelomere analysis in Tunisian mentally retarded patients. [electronic resource] by Hila, Lamia Tébourbi, Hédia Abaied, Leila Rejeb, Imène Ben Jemaa, Lamia Chaabouni, Habiba Producer: 20091211 In: Biochemical genetics vol. 47 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Autosomal recessive acro-fronto-facio-nasal dysostosis associated with genitourinary anomalies: a third case report. [electronic resource] by Chaabouni, Myriam Maazoul, Faouzi Ben Hamida, Amira Berhouma, Moncef Marrakchi, Zahra Chaabouni, Habiba Producer: 20080820 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Coexistence of Behçet's disease with ankylosing spondylitis and familial Mediterranean fever: a rare occurrence. [electronic resource] by Frigui, Makram Kechaou, Manel Jallouli, Moez Kaddour, Neila Chaabouni, Habiba Bouhamed Bahloul, Zouhir Producer: 20140425 In: Clinics and practice vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation. [electronic resource] by Chograni, Manèl Chaabouni, Myriam Mâazoul, Faouzi Bouzid, Hedi Kraiem, Abdelhafid Chaabouni, Habiba B Bouhamed Producer: 20120306 In: BMC ophthalmology vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Exploring the 7p22.1 chromosome as a candidate region for autism. [electronic resource] by Bayou, Nadia Belhadj, Ahlem Daoud, Hussein Briault, Sylvain Helayem, M Bechir Chaabouni, Habiba M'rad, Ridha Producer: 20100727 In: Journal of biomedicine & biotechnology vol. 2010 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Pallister-Killian syndrome with additional manifestations of cleft palate and sacral appendage. [electronic resource] by Chaouachi, Sihem Ben Hamida, Emira Ennine, Ines Chaabouni, Meriem Sfar, Rachida Chaabouni, Habiba Marrakchi, Zahra Producer: 20101025 In: La Tunisie medicale vol. 88 Availability: No items available. Save to lists Add to cart (remove)
	15.	[Molecular diagnosis of fragile X syndrome]. [electronic resource] by Ben Jemaa, Lamia Khemir, Samah Maazoul, Faouzi Richard, Laurent Beldjord, Cherif Chaabouni, Myriam Chaabouni, Habiba Producer: 20090313 In: La Tunisie medicale vol. 86 Availability: No items available. Save to lists Add to cart (remove)
	16.	Mutation analysis of TBX22 reveals new mutation in Tunisian CPX family. [electronic resource] by Chaabouni, Myriam Smaoui, Nizar Benneji, Neila M'rad, Ridha Jemaa, Lamia Ben Hachicha, Slah Chaabouni, Habiba Producer: 20050526 In: Clinical dysmorphology vol. 14 Availability: No items available. Save to lists Add to cart (remove)
	17.	GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness. [electronic resource] by Trabelsi, Mediha Bahri, Wafa Habibi, Marwene Zainine, Rim Maazoul, Faouzi Ghazi, Besbes Chaabouni, Habiba Mrad, Ridha Producer: 20131213 In: International journal of pediatric otorhinolaryngology vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Molecular genetic analysis of Tunisian patients with a classic form of 21-hydroxylase deficiency: identification of four novel mutations and high prevalence of Q318X mutation. [electronic resource] by Kharrat, Maher Tardy, Véronique M'Rad, Ridha Maazoul, Faouzi Jemaa, Lamia Ben Refaï, Mohamed Morel, Yves Chaabouni, Habiba Producer: 20040211 In: The Journal of clinical endocrinology and metabolism vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	19.	[Treacher-Collins syndrome: clinical and genetic aspects apropos of 4 cases of which 1 is familial]. [electronic resource] by Chaabouni, Myriam Fersi, Mounir Belghith, Neila Maazoul, Faouzi M'rad, Ridha Ben Jemaa, Lamia Gandoura, Najoua Chaabouni, Habiba Producer: 20080307 In: La Tunisie medicale vol. 85 Availability: No items available. Save to lists Add to cart (remove)
	20.	A novel frame shift mutation in the PQBP1 gene identified in a Tunisian family with X-linked mental retardation. [electronic resource] by Rejeb, Imen Ben Jemaa, Lamia Abaied, Leila Kraoua, Lilia Saillour, Yoann Maazoul, Faouzi Chelly, Jamel Chaabouni, Habiba Producer: 20110928 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 44 results.