Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

249 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum.
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. Messaoud O, et al. Among authors: abdelhak s. Public Health Genomics. 2013;16(5):251-4. doi: 10.1159/000354584. Epub 2013 Sep 7. Public Health Genomics. 2013. PMID: 24021614
Gene Symbol: ars. Disease: Mal de Meleda.
Abdelhak S, Charfeddine C, Mokni M, Mousli RB, Elkares R, Bouchlaka C, Boubaker S, Ghedamsi S, Baccouche D, Osman AB, Dellagi K. Abdelhak S, et al. Hum Genet. 2004 May;114(6):609. Hum Genet. 2004. PMID: 15176391 No abstract available.
Fanconi anemia: contribution of molecular analyses to the identification of bone marrow graft donors and the study of chimerism in grafted patients.
Bouchlaka C, Othman TB, Aissaoui L, Elloumi H, Elloumi M, Amouri A, Abid HB, Hadiji S, Slama H, Makni H, Saad A, Abdelhak S, Dellagi K; Tunisian Fanconi Anemia Study Group. Bouchlaka C, et al. Among authors: abdelhak s. Genet Test. 2004 Fall;8(3):268-75. doi: 10.1089/gte.2004.8.268. Genet Test. 2004. PMID: 15727250
Clinical and mutational investigations of tyrosinemia type II in Northern Tunisia: identification and structural characterization of two novel TAT mutations.
Charfeddine C, Monastiri K, Mokni M, Laadjimi A, Kaabachi N, Perin O, Nilges M, Kassar S, Keirallah M, Guediche MN, Kamoun MR, Tebib N, Ben Dridi MF, Boubaker S, Ben Osman A, Abdelhak S. Charfeddine C, et al. Among authors: abdelhak s. Mol Genet Metab. 2006 Jun;88(2):184-91. doi: 10.1016/j.ymgme.2006.02.006. Epub 2006 Mar 30. Mol Genet Metab. 2006. PMID: 16574453
Immunohistological study of involucrin expression in Darier's disease skin.
Kassar S, Charfeddine C, Zribi H, Tounsi-Kettiti H, Bchetnia M, Jerbi E, Cassio D, Mokni M, Abdelhak S, Ben Osman A, Boubaker S. Kassar S, et al. Among authors: abdelhak s. J Cutan Pathol. 2008 Jul;35(7):635-40. doi: 10.1111/j.1600-0560.2007.00880.x. Epub 2008 Feb 29. J Cutan Pathol. 2008. PMID: 18312435
249 results