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249 results

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Page 1
Consanguinity, endogamy, and genetic disorders in Tunisia.
Ben Halim N, Ben Alaya Bouafif N, Romdhane L, Kefi Ben Atig R, Chouchane I, Bouyacoub Y, Arfa I, Cherif W, Nouira S, Talmoudi F, Lasram K, Hsouna S, Ghazouani W, Azaiez H, El Matri L, Abid A, Tebib N, Ben Dridi MF, Kachboura S, Amouri A, Mokni M, Ben Arab S, Dellagi K, Abdelhak S. Ben Halim N, et al. Among authors: abdelhak s. J Community Genet. 2013 Apr;4(2):273-84. doi: 10.1007/s12687-012-0128-7. Epub 2012 Dec 4. J Community Genet. 2013. PMID: 23208456 Free PMC article. No abstract available.
Heterozygous manifestations in female carriers of Mal de Meleda.
Mokni M, Charfeddine C, Ben Mously R, Baccouche D, Kaabi B, Ben Osman A, Dellagi K, Abdelhak S. Mokni M, et al. Among authors: abdelhak s. Clin Genet. 2004 Mar;65(3):244-6. doi: 10.1111/j.0009-9163.2004.00224.x. Clin Genet. 2004. PMID: 14756676 No abstract available.
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.
[Molecular study of Fanconi anemia in Tunisia].
Bouchlaka C, Abdelhak S, Dellagi K; Groupe d'Etude de la Maladie de Fanconi en Tunisie. Bouchlaka C, et al. Among authors: abdelhak s. Tunis Med. 2004 May;82(5):402-10. Tunis Med. 2004. PMID: 15453041 French.
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
249 results