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Identity-by-descent-guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy.
Coppieters F, Van Schil K, Bauwens M, Verdin H, De Jaegher A, Syx D, Sante T, Lefever S, Abdelmoula NB, Depasse F, Casteels I, de Ravel T, Meire F, Leroy BP, De Baere E. Coppieters F, et al. Among authors: abdelmoula nb. Genet Med. 2014 Sep;16(9):671-80. doi: 10.1038/gim.2014.24. Epub 2014 Mar 13. Genet Med. 2014. PMID: 24625443 Free article.
Clinical and Molecular Findings of Tunisian Patients with RASopathies.
Louati R, Abdelmoula NB, Trabelsi I, Abid D, Lissewski C, Kharrat N, Kamoun S, Zenker M, Rebai T. Louati R, et al. Among authors: abdelmoula nb. Mol Syndromol. 2014 Aug;5(5):212-7. doi: 10.1159/000362898. Epub 2014 May 23. Mol Syndromol. 2014. PMID: 25337068 Free PMC article.
Non-classical human leukocyte antigen class I in Tunisian children with autism.
Kharrat N, Abdelhedi R, Gtif I, Ayadi I, Rizzo R, Bortolotti D, Abdelmoula NB, Ghribi F, Rebai A, Zidi I. Kharrat N, et al. Among authors: abdelmoula nb. Cent Eur J Immunol. 2020;45(2):176-183. doi: 10.5114/ceji.2020.97906. Epub 2020 Jul 27. Cent Eur J Immunol. 2020. PMID: 33456328 Free PMC article.
Evaluation of DAZ microdeletions in 34 infertile men.
Abdelmoula NB, Sallemi A, Chakroun N, Keskes L, Amouri A, Rebai T. Abdelmoula NB, et al. Arch Androl. 2006 May-Jun;52(3):175-8. doi: 10.1080/01485010500316261. Arch Androl. 2006. PMID: 16574598
16 results