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Comparison of two next-generation sequencing kits for diagnosis of epileptic disorders with a user-friendly tool for displaying gene coverage, DeCovA.
Dimassi S, Simonet T, Labalme A, Boutry-Kryza N, Campan-Fournier A, Lamy R, Bardel C, Elsensohn MH, Roucher-Boulez F, Chatron N, Putoux A, de Bellescize J, Ville D, Schaeffer L, Roy P, Mougou-Zerelli S, Saad A, Calender A, Sanlaville D, Lesca G. Dimassi S, et al. Among authors: saad a. Appl Transl Genom. 2015 Oct 17;7:19-25. doi: 10.1016/j.atg.2015.10.001. eCollection 2015 Dec. Appl Transl Genom. 2015. PMID: 27054081 Free PMC article.
Array-CGH study of partial trisomy 9p without mental retardation.
Bouhjar IB, Hannachi H, Zerelli SM, Labalme A, Gmidène A, Soyah N, Missaoui S, Sanlaville D, Elghezal H, Saad A. Bouhjar IB, et al. Among authors: saad a. Am J Med Genet A. 2011 Jul;155A(7):1735-9. doi: 10.1002/ajmg.a.34044. Epub 2011 May 27. Am J Med Genet A. 2011. PMID: 21626676
Relationship between sperm aneuploidy, sperm DNA integrity, chromatin packaging, traditional semen parameters, and recurrent pregnancy loss.
Zidi-Jrah I, Hajlaoui A, Mougou-Zerelli S, Kammoun M, Meniaoui I, Sallem A, Brahem S, Fekih M, Bibi M, Saad A, Ibala-Romdhane S. Zidi-Jrah I, et al. Among authors: saad a. Fertil Steril. 2016 Jan;105(1):58-64. doi: 10.1016/j.fertnstert.2015.09.041. Epub 2015 Oct 19. Fertil Steril. 2016. PMID: 26493117 Free article.
Partial KCNQ1OT1 hypomethylation: A disguised familial Beckwith-Wiedemann syndrome as a sporadic adrenocortical tumor.
H'mida Ben-Brahim D, Hammami S, Haddaji Mastouri M, Trabelsi S, Chourabi M, Sassi S, Mougou S, Gribaa M, Zakhama A, Guédiche MN, Saad A. H'mida Ben-Brahim D, et al. Among authors: saad a. Appl Transl Genom. 2014 Oct 15;4:1-3. doi: 10.1016/j.atg.2014.10.001. eCollection 2015 Mar. Appl Transl Genom. 2014. PMID: 26937341 Free PMC article.
2,151 results