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H Chaabouni

Showing results (41-50 of 55) with videos related to

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Annales De Dermatologie Et De Venereologie|June 1, 2005
[Junctional congenital bullous epidermolysis, cutaneous aplasia and pyloric atresia]A Cherif, F Cherif, F Siala-Guagi, et al.
Physical Review Letters|August 20, 2013
Quantum tunneling of oxygen atoms on very cold surfacesM Minissale, E Congiu, S Baouche, et al.
Clinical Genetics|March 19, 2010
FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndromeL Kraoua, M Chaabouni, M Trabelsi, et al.
La Tunisie Medicale|January 5, 2002
[Intestinal metaplasia at the gastroesophageal junction - epidemiologic and histologic aspects. Report of 164 cases]H Chaabouni, S Haouet, I Cheikh, et al.
Clinical Genetics|December 31, 2013
Mutation spectrum and prevalence of BRCA1 and BRCA2 genes in patients with familial and early-onset breast/ovarian cancer from TunisiaA Riahi, M Kharrat, M E Ghourabi, et al.
Annales D'Endocrinologie|June 11, 2008
[Genetic analysis of Turner syndrome: 89 cases in Tunisia]I Kammoun, M Chaabouni, M Trabelsi, et al.
Pathologie-Biologie|December 3, 2008
[Late revelation of homocysteinuria: clinical, biological and progressive aspects]S Azzabi, A Barhoumi, S Omar, et al.
The Journal of Chemical Physics|December 27, 2012
Water formation through O2 + D pathway on cold silicate and amorphous water ice surfaces of interstellar interestH Chaabouni, M Minissale, G Manicò, et al.
Clinical Genetics|March 25, 2010
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379VM Kharrat, S Trabelsi, M Chaabouni, et al.
Clinical Genetics|February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosisO M'hamdi, C Redin, C Stoetzel, et al.
Pageof 6

Showing results (41-50 of 55) with videos related to

Sort By:
Pageof 6
Annales De Dermatologie Et De Venereologie|June 1, 2005
[Junctional congenital bullous epidermolysis, cutaneous aplasia and pyloric atresia]A Cherif, F Cherif, F Siala-Guagi, et al.
Physical Review Letters|August 20, 2013
Quantum tunneling of oxygen atoms on very cold surfacesM Minissale, E Congiu, S Baouche, et al.
Clinical Genetics|March 19, 2010
FOXL2 mutations in Tunisian patients with blepharophimosis-ptosis-epicanthus inversus syndromeL Kraoua, M Chaabouni, M Trabelsi, et al.
La Tunisie Medicale|January 5, 2002
[Intestinal metaplasia at the gastroesophageal junction - epidemiologic and histologic aspects. Report of 164 cases]H Chaabouni, S Haouet, I Cheikh, et al.
Clinical Genetics|December 31, 2013
Mutation spectrum and prevalence of BRCA1 and BRCA2 genes in patients with familial and early-onset breast/ovarian cancer from TunisiaA Riahi, M Kharrat, M E Ghourabi, et al.
Annales D'Endocrinologie|June 11, 2008
[Genetic analysis of Turner syndrome: 89 cases in Tunisia]I Kammoun, M Chaabouni, M Trabelsi, et al.
Pathologie-Biologie|December 3, 2008
[Late revelation of homocysteinuria: clinical, biological and progressive aspects]S Azzabi, A Barhoumi, S Omar, et al.
The Journal of Chemical Physics|December 27, 2012
Water formation through O2 + D pathway on cold silicate and amorphous water ice surfaces of interstellar interestH Chaabouni, M Minissale, G Manicò, et al.
Clinical Genetics|March 25, 2010
Only two mutations detected in 15 Tunisian patients with 11β-hydroxylase deficiency: the p.Q356X and the novel p.G379VM Kharrat, S Trabelsi, M Chaabouni, et al.
Clinical Genetics|February 26, 2013
Clinical and genetic characterization of Bardet-Biedl syndrome in Tunisia: defining a strategy for molecular diagnosisO M'hamdi, C Redin, C Stoetzel, et al.
Pageof 6