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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: rouba h. PLoS One. 2012;7(3):e34111. doi: 10.1371/journal.pone.0034111. Epub 2012 Mar 23. PLoS One. 2012. PMID: 22457816 Free PMC article.
A high frequency of Y chromosome deletions in males with nonidiopathic infertility.
Krausz C, Quintana-Murci L, Barbaux S, Siffroi JP, Rouba H, Delafontaine D, Souleyreau-Therville N, Arvis G, Antoine JM, Erdei E, Taar JP, Tar A, Jeandidier E, Plessis G, Bourgeron T, Dadoune JP, Fellous M, McElreavey K. Krausz C, et al. Among authors: rouba h. J Clin Endocrinol Metab. 1999 Oct;84(10):3606-12. doi: 10.1210/jcem.84.10.6040. J Clin Endocrinol Metab. 1999. PMID: 10523003
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: rouba h. J Urol. 2007 May;177(5):1947-51. doi: 10.1016/j.juro.2007.01.002. J Urol. 2007. PMID: 17437853
GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
Abidi O, Boulouiz R, Nahili H, Ridal M, Alami MN, Tlili A, Rouba H, Masmoudi S, Chafik A, Hassar M, Barakat A. Abidi O, et al. Among authors: rouba h. Int J Pediatr Otorhinolaryngol. 2007 Aug;71(8):1239-45. doi: 10.1016/j.ijporl.2007.04.019. Epub 2007 Jun 5. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17553572
67 results