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Dermatology Online Journal
|
August 21, 2008
Supernumerary nipples in association with Hailey-Hailey disease in a Tunisian family
R 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 diagnosis
M 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 severity
O 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 families
C 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 pigmentosum
O 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 mutations
C Charfeddine, K Monastiri, M Mokni, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 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 family
R 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 diagnosis
M 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 severity
O 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 families
C 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 pigmentosum
O 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 mutations
C Charfeddine, K Monastiri, M Mokni, et al.
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of 5