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O Messaoud

Showing results (1-10 of 6) with videos related to

Pageof 1
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Gene|March 14, 2013
Biotinidase deficiency: novel mutations in Algerian patientsA Tiar, A Mekki, M Nagara, 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.
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.
The British Journal of Dermatology|March 5, 2010
Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian familyO Messaoud, M Ben Rekaya, R Kefi, 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.
Clinical Genetics|May 27, 2015
Comorbidity in the Tunisian populationL Romdhane, O Messaoud, Y Bouyacoub, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Gene|March 14, 2013
Biotinidase deficiency: novel mutations in Algerian patientsA Tiar, A Mekki, M Nagara, 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.
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.
The British Journal of Dermatology|March 5, 2010
Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian familyO Messaoud, M Ben Rekaya, R Kefi, 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.
Clinical Genetics|May 27, 2015
Comorbidity in the Tunisian populationL Romdhane, O Messaoud, Y Bouyacoub, et al.
Pageof 1