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Mutations in TPRN cause a progressive form of autosomal-recessive nonsyndromic hearing loss.
Li Y, Pohl E, Boulouiz R, Schraders M, Nürnberg G, Charif M, Admiraal RJ, von Ameln S, Baessmann I, Kandil M, Veltman JA, Nürnberg P, Kubisch C, Barakat A, Kremer H, Wollnik B. Li Y, et al. Among authors: charif m. Am J Hum Genet. 2010 Mar 12;86(3):479-84. doi: 10.1016/j.ajhg.2010.02.003. Epub 2010 Feb 18. Am J Hum Genet. 2010. PMID: 20170898 Free PMC article.
Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.
Benrahma H, Arfa I, Charif M, Bounaceur S, Eloualid A, Boulouiz R, Nahili H, Abidi O, Rouba H, Chadli A, Oudghiri M, Farouqui A, Abdelhak S, Barakat A. Benrahma H, et al. Among authors: charif m. J Community Health. 2011 Dec;36(6):943-8. doi: 10.1007/s10900-011-9393-3. J Community Health. 2011. PMID: 21442339
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: charif m. 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: charif m. PLoS One. 2012;7(4):e34902. doi: 10.1371/journal.pone.0034902. Epub 2012 Apr 13. PLoS One. 2012. PMID: 22514689 Free PMC article.
151 results