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High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis.
Published in:
Journal of Human Genetics, 2009, v. 54, n. 7, p. 426, doi. 10.1038/jhg.2009.50
By:
- Rekaya, M. Ben;
- Messaoud, O.;
- Talmoudi, F.;
- Nouira, S.;
- Ouragini, H.;
- Amouri, A.;
- Boussen, H.;
- Boubaker, S.;
- Mokni, M.;
- Mokthar, I.;
- Abdelhak, S.;
- Zghal, M.
Publication type:
Article
The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of Xeroderma pigmentosum.
Published in:
Public Health Genomics, 2013, v. 16, n. 5, p. 251, doi. 10.1159/000354584
By:
- Messaoud, O.;
- Ben Rekaya, M.;
- Jerbi, M.;
- Ouertani, I.;
- Kefi, R.;
- Laroussi, N.;
- Bouyacoub, Y.;
- Benfadhel, S.;
- Yacoub-Youssef, H.;
- Boubaker, S.;
- Zghal, M.;
- Mrad, R.;
- amouri, a.;
- abdelhak, S.
Publication type:
Article
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.
Published in:
Archives of Dermatological Research, 2012, v. 304, n. 2, p. 171, doi. 10.1007/s00403-011-1190-4
By:
- Messaoud, O.;
- Ben Rekaya, M.;
- Ouragini, H.;
- Benfadhel, S.;
- Azaiez, H.;
- Kefi, R.;
- Gouider-Khouja, N.;
- Mokhtar, I.;
- Amouri, A.;
- Boubaker, M.;
- Zghal, M.;
- Abdelhak, S.
Publication type:
Article
Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia.
Published in:
British Journal of Dermatology, 2016, v. 174, n. 2, p. 439, doi. 10.1111/bjd.14046
By:
- Jerbi, M.;
- Ben Rekaya, M.;
- Naouali, C.;
- Jones, M.;
- Messaoud, O.;
- Tounsi, H.;
- Nagara, M.;
- Chargui, M.;
- Kefi, R.;
- Boussen, H.;
- Mokni, M.;
- Mrad, R.;
- Boubaker, M.S.;
- Abdelhak, S.;
- Khaled, A.;
- Zghal, M.;
- Yacoub ‐ Youssef, H.
Publication type:
Article
Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.
Published in:
British Journal of Dermatology, 2010, v. 162, n. 4, p. 883, doi. 10.1111/j.1365-2133.2010.09646.x
By:
- Messaoud, O.;
- Ben Rekaya, M.;
- Kefi, R.;
- Chebel, S.;
- Boughammoura-Bouatay, A.;
- Bel Hadj Ali, H.;
- Gouider-Khouja, N.;
- Zili, J.;
- Frih-Ayed, M.;
- Mokhtar, I.;
- Abdelhak, S.;
- Zghal, M.
Publication type:
Article

Found: 5

High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis.

The Experience of a Tunisian Referral Centre in Prenatal Diagnosis of Xeroderma pigmentosum.

Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.

Clinical, genealogical and molecular investigation of the xeroderma pigmentosum type C complementation group in Tunisia.

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.