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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 2
2000 2
2001 3
2003 3
2004 3
2005 1
2007 4
2009 1
2010 3
2024 0

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22 results

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Page 1
Genetic screening for deafness.
Smith RJ, Hone S. Smith RJ, et al. Pediatr Clin North Am. 2003 Apr;50(2):315-29. doi: 10.1016/s0031-3955(03)00026-9. Pediatr Clin North Am. 2003. PMID: 12809325 Review.
Clinical aspects of hereditary hearing loss.
Kochhar A, Hildebrand MS, Smith RJ. Kochhar A, et al. Genet Med. 2007 Jul;9(7):393-408. doi: 10.1097/gim.0b013e3180980bd0. Genet Med. 2007. PMID: 17666886 Free article. Review.
Autosomal dominant nonsyndromic hearing impairment.
Van Laer L, McGuirt WT, Yang T, Smith RJ, Van Camp G. Van Laer L, et al. Am J Med Genet. 1999 Sep 24;89(3):167-74. doi: 10.1002/(sici)1096-8628(19990924)89:3<167::aid-ajmg7>3.3.co;2-m. Am J Med Genet. 1999. PMID: 10704191 Review.
The DFNA10 phenotype.
De Leenheer EM, Huygen PL, Wayne S, Smith RJ, Cremers CW. De Leenheer EM, et al. Ann Otol Rhinol Laryngol. 2001 Sep;110(9):861-6. doi: 10.1177/000348940111000910. Ann Otol Rhinol Laryngol. 2001. PMID: 11558763
Maternally inherited hearing impairment.
Van Camp G, Smith RJ. Van Camp G, et al. Clin Genet. 2000 Jun;57(6):409-14. doi: 10.1034/j.1399-0004.2000.570601.x. Clin Genet. 2000. PMID: 10905659 Review.
Genetic male infertility and mutation of CATSPER ion channels.
Hildebrand MS, Avenarius MR, Fellous M, Zhang Y, Meyer NC, Auer J, Serres C, Kahrizi K, Najmabadi H, Beckmann JS, Smith RJ. Hildebrand MS, et al. Eur J Hum Genet. 2010 Nov;18(11):1178-84. doi: 10.1038/ejhg.2010.108. Epub 2010 Jul 21. Eur J Hum Genet. 2010. PMID: 20648059 Free PMC article. Review.
miRNA mutations are not a common cause of deafness.
Hildebrand MS, Witmer PD, Xu S, Newton SS, Kahrizi K, Najmabadi H, Valle D, Smith RJ. Hildebrand MS, et al. Am J Med Genet A. 2010 Mar;152A(3):646-52. doi: 10.1002/ajmg.a.33299. Am J Med Genet A. 2010. PMID: 20186779 Free PMC article.
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).
McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ. McGuirt WT, et al. Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516. Nat Genet. 1999. PMID: 10581026
A novel DFNA5 mutation does not cause hearing loss in an Iranian family.
Van Laer L, Meyer NC, Malekpour M, Riazalhosseini Y, Moghannibashi M, Kahrizi K, Vandevelde A, Alasti F, Najmabadi H, Van Camp G, Smith RJH. Van Laer L, et al. J Hum Genet. 2007;52(6):549-552. doi: 10.1007/s10038-007-0137-2. Epub 2007 Apr 11. J Hum Genet. 2007. PMID: 17427029
22 results