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Showing results (41-50 of 47) with videos related to

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Dermatology Online Journal|August 21, 2008
Supernumerary nipples in association with Hailey-Hailey disease in a Tunisian familyR Benmously-Mlika, S Deghais, M Bchetnia, et al.
Journal of Human Genetics|May 30, 2009
High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosisM Ben Rekaya, O Messaoud, F Talmoudi, et al.
Annales De Dermatologie Et De Venereologie|December 17, 2004
[Pemphigoid gestationis: a study of 20 cases]M Mokni, M Fourati, I Karoui, et al.
Archives of Dermatological Research|November 15, 2011
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severityO Messaoud, M Ben Rekaya, H Ouragini, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 13, 2016
Clinical and molecular investigation of Buschke-Fischer-Brauer in consanguineous Tunisian familiesC Charfeddine, C Ktaifi, N Laroussi, et al.
Public Health Genomics|September 12, 2013
The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosumO Messaoud, M Ben Rekaya, M Jerbi, et al.
Molecular Genetics and Metabolism|April 1, 2006
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutationsC Charfeddine, K Monastiri, M Mokni, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Dermatology Online Journal|August 21, 2008
Supernumerary nipples in association with Hailey-Hailey disease in a Tunisian familyR Benmously-Mlika, S Deghais, M Bchetnia, et al.
Journal of Human Genetics|May 30, 2009
High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosisM Ben Rekaya, O Messaoud, F Talmoudi, et al.
Annales De Dermatologie Et De Venereologie|December 17, 2004
[Pemphigoid gestationis: a study of 20 cases]M Mokni, M Fourati, I Karoui, et al.
Archives of Dermatological Research|November 15, 2011
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severityO Messaoud, M Ben Rekaya, H Ouragini, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 13, 2016
Clinical and molecular investigation of Buschke-Fischer-Brauer in consanguineous Tunisian familiesC Charfeddine, C Ktaifi, N Laroussi, et al.
Public Health Genomics|September 12, 2013
The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosumO Messaoud, M Ben Rekaya, M Jerbi, et al.
Molecular Genetics and Metabolism|April 1, 2006
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutationsC Charfeddine, K Monastiri, M Mokni, et al.
Pageof 5