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Ines Ouertani

Showing results (1-10 of 12) with videos related to

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Journal of Community Genetics|November 24, 2011
Prevalence of Bardet-Biedl syndrome in TunisiaOussama M'hamdi, Ines Ouertani, Faouzi Maazoul, et al.
Fetal and Pediatric Pathology|November 11, 2023
Partial Trisomy 4p Syndrome Diagnosed PrenatallyKaouther Nasri, Nadia Ben Jamaa, Ines Ouertani, et al.
European Journal of Medical Genetics|February 12, 2022
3M syndrome: A Tunisian seven-cases seriesKhaoula Khachnaoui-Zaafrane, Ines Ouertani, Amira Zanati, et al.
Fetal and Pediatric Pathology|July 25, 2025
Broad Clinical Spectrum of Mosaic Trisomy 2: Report of Two New Cases in TunisiaKaouther Nasri, Nadia Ben Jamaa, Ines Ouertani, et al.
The Pan African Medical Journal|September 2, 2015
Perinatal-lethal Gaucher disease presenting as hydrops fetalisEmira BenHamida, Imene Ayadi, Ines Ouertani, et al.
European Journal of Medical Genetics|November 13, 2012
Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategyMediha Trabelsi, Imen Chelly, Faouzi Maazoul, et al.
European Journal of Medical Genetics|May 31, 2011
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case reportLilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, et al.
European Journal of Medical Genetics|May 20, 2009
A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasiaInes Ouertani, Myriam Chaabouni, Ilhem Turki, et al.
International Journal of Pediatric Otorhinolaryngology|December 12, 2017
Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patientsMediha Trabelsi, Malek Nouira, Faouzi Maazoul, et al.
European Journal of Medical Genetics|October 14, 2018
WDR73-related galloway mowat syndrome with collapsing glomerulopathyMariem El Younsi, Lilia Kraoua, Rym Meddeb, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Community Genetics|November 24, 2011
Prevalence of Bardet-Biedl syndrome in TunisiaOussama M'hamdi, Ines Ouertani, Faouzi Maazoul, et al.
Fetal and Pediatric Pathology|November 11, 2023
Partial Trisomy 4p Syndrome Diagnosed PrenatallyKaouther Nasri, Nadia Ben Jamaa, Ines Ouertani, et al.
European Journal of Medical Genetics|February 12, 2022
3M syndrome: A Tunisian seven-cases seriesKhaoula Khachnaoui-Zaafrane, Ines Ouertani, Amira Zanati, et al.
Fetal and Pediatric Pathology|July 25, 2025
Broad Clinical Spectrum of Mosaic Trisomy 2: Report of Two New Cases in TunisiaKaouther Nasri, Nadia Ben Jamaa, Ines Ouertani, et al.
The Pan African Medical Journal|September 2, 2015
Perinatal-lethal Gaucher disease presenting as hydrops fetalisEmira BenHamida, Imene Ayadi, Ines Ouertani, et al.
European Journal of Medical Genetics|November 13, 2012
Epidemiologic and clinical characteristics of 458 Tunisian patients with intellectual deficiency and a reconsidered diagnostic strategyMediha Trabelsi, Imen Chelly, Faouzi Maazoul, et al.
European Journal of Medical Genetics|May 31, 2011
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case reportLilia Kraoua, Myriam Chaabouni, Elisabeth Ewers, et al.
European Journal of Medical Genetics|May 20, 2009
A 24-Mb deletion in 14q in a girl with corpus callosum hypoplasiaInes Ouertani, Myriam Chaabouni, Ilhem Turki, et al.
International Journal of Pediatric Otorhinolaryngology|December 12, 2017
Novel PAX3 mutations causing Waardenburg syndrome type 1 in Tunisian patientsMediha Trabelsi, Malek Nouira, Faouzi Maazoul, et al.
European Journal of Medical Genetics|October 14, 2018
WDR73-related galloway mowat syndrome with collapsing glomerulopathyMariem El Younsi, Lilia Kraoua, Rym Meddeb, et al.
Pageof 2