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Page 1
Association of the MTHFR A1298C variant with unexplained severe male infertility.
Eloualid A, Abidi O, Charif M, El Houate B, Benrahma H, Louanjli N, Chadli E, Ajjemami M, Barakat A, Bashamboo A, McElreavey K, Rhaissi H, Rouba H. Eloualid A, et al. Among authors: chadli e. PLoS One. 2012;7(3):e34111. doi: 10.1371/journal.pone.0034111. Epub 2012 Mar 23. PLoS One. 2012. PMID: 22457816 Free PMC article.
Association of spermatogenic failure with the b2/b3 partial AZFc deletion.
Eloualid A, Rhaissi H, Reguig A, Bounaceur S, El Houate B, Abidi O, Charif M, Louanjli N, Chadli E, Barakat A, Bashamboo A, McElreavey K, Rouba H. Eloualid A, et al. Among authors: chadli e. PLoS One. 2012;7(4):e34902. doi: 10.1371/journal.pone.0034902. Epub 2012 Apr 13. PLoS One. 2012. PMID: 22514689 Free PMC article.
Cytogenetic Profile of Moroccan Pediatric Acute Lymphoblastic Leukemia: Analysis of 155 Cases With a Review of the Literature.
Chebihi ZT, Belkhayat A, Chadli E, Hilal L, Skhoun H, Hessissen L, El Khorassani M, El Kababri M, Kili A, Khattab M, Bakri Y, Dakka N. Chebihi ZT, et al. Among authors: chadli e. Clin Lymphoma Myeloma Leuk. 2018 Jun;18(6):e241-e248. doi: 10.1016/j.clml.2018.04.004. Epub 2018 Apr 25. Clin Lymphoma Myeloma Leuk. 2018. PMID: 29748040 Review.
Three new BLM gene mutations associated with Bloom syndrome.
Amor-Guéret M, Dubois-d'Enghien C, Laugé A, Onclercq-Delic R, Barakat A, Chadli E, Bousfiha AA, Benjelloun M, Flori E, Doray B, Laugel V, Lourenço MT, Gonçalves R, Sousa S, Couturier J, Stoppa-Lyonnet D. Amor-Guéret M, et al. Among authors: chadli e. Genet Test. 2008 Jun;12(2):257-61. doi: 10.1089/gte.2007.0119. Genet Test. 2008. PMID: 18471088
Novel mutations involving the INSL3 gene associated with cryptorchidism.
El Houate B, Rouba H, Sibai H, Barakat A, Chafik A, Chadli el B, Imken L, Bogatcheva NV, Feng S, Agoulnik AI, McElreavey K. El Houate B, et al. Among authors: chadli el b. J Urol. 2007 May;177(5):1947-51. doi: 10.1016/j.juro.2007.01.002. J Urol. 2007. PMID: 17437853