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Page 1
Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment.
Collin RW, Kalay E, Oostrik J, Caylan R, Wollnik B, Arslan S, den Hollander AI, Birinci Y, Lichtner P, Strom TM, Toraman B, Hoefsloot LH, Cremers CW, Brunner HG, Cremers FP, Karaguzel A, Kremer H. Collin RW, et al. Among authors: arslan s. Hum Mutat. 2007 Jul;28(7):718-23. doi: 10.1002/humu.20510. Hum Mutat. 2007. PMID: 17373699
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
Collin RW, Kalay E, Tariq M, Peters T, van der Zwaag B, Venselaar H, Oostrik J, Lee K, Ahmed ZM, Caylan R, Li Y, Spierenburg HA, Eyupoglu E, Heister A, Riazuddin S, Bahat E, Ansar M, Arslan S, Wollnik B, Brunner HG, Cremers CW, Karaguzel A, Ahmad W, Cremers FP, Vriend G, Friedman TB, Riazuddin S, Leal SM, Kremer H. Collin RW, et al. Among authors: arslan s. Am J Hum Genet. 2008 Jan;82(1):125-38. doi: 10.1016/j.ajhg.2007.09.008. Am J Hum Genet. 2008. PMID: 18179891 Free PMC article.
A rare case of gingival myiasis in a 2-year-old child.
Arslan S, Islamoğlu A, Çobanoğlu B. Arslan S, et al. Int J Paediatr Dent. 2013 Sep;23(5):387-8. doi: 10.1111/ipd.12033. Epub 2013 Apr 16. Int J Paediatr Dent. 2013. PMID: 23590529
Giant sialolith of submandibular gland: report of a case†.
Arslan S, Vuralkan E, Çobanog˘lu B, Arslan A, Ural A. Arslan S, et al. Among authors: arslan a. J Surg Case Rep. 2015 Apr 5;2015(4):rjv043. doi: 10.1093/jscr/rjv043. J Surg Case Rep. 2015. PMID: 25848088 Free PMC article.
1,082 results