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

Year Number of Results
1999 3
2000 5
2001 6
2002 4
2003 3
2004 2
2005 6
2006 3
2007 6
2008 1
2009 3
2010 3
2024 0

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41 results

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Page 1
GJB2 mutations and degree of hearing loss: a multicenter study.
Snoeckx RL, Huygen PL, Feldmann D, Marlin S, Denoyelle F, Waligora J, Mueller-Malesinska M, Pollak A, Ploski R, Murgia A, Orzan E, Castorina P, Ambrosetti U, Nowakowska-Szyrwinska E, Bal J, Wiszniewski W, Janecke AR, Nekahm-Heis D, Seeman P, Bendova O, Kenna MA, Frangulov A, Rehm HL, Tekin M, Incesulu A, Dahl HH, du Sart D, Jenkins L, Lucas D, Bitner-Glindzicz M, Avraham KB, Brownstein Z, del Castillo I, Moreno F, Blin N, Pfister M, Sziklai I, Toth T, Kelley PM, Cohn ES, Van Maldergem L, Hilbert P, Roux AF, Mondain M, Hoefsloot LH, Cremers CW, Löppönen T, Löppönen H, Parving A, Gronskov K, Schrijver I, Roberson J, Gualandi F, Martini A, Lina-Granade G, Pallares-Ruiz N, Correia C, Fialho G, Cryns K, Hilgert N, Van de Heyning P, Nishimura CJ, Smith RJ, Van Camp G. Snoeckx RL, et al. Am J Hum Genet. 2005 Dec;77(6):945-57. doi: 10.1086/497996. Epub 2005 Oct 19. Am J Hum Genet. 2005. PMID: 16380907 Free PMC article.
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.
Genetic screening for hearing loss.
Hone SW, Smith RJ. Hone SW, et al. Clin Otolaryngol Allied Sci. 2003 Aug;28(4):285-90. doi: 10.1046/j.1365-2273.2003.00700.x. Clin Otolaryngol Allied Sci. 2003. PMID: 12871240 Review.
The role of connexins in human disease.
Chang EH, Van Camp G, Smith RJ. Chang EH, et al. Ear Hear. 2003 Aug;24(4):314-23. doi: 10.1097/01.AUD.0000079801.55588.13. Ear Hear. 2003. PMID: 12923422 Review.
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.
Autosomal recessive nonsyndromic hearing loss.
Sundstrom RA, Van Laer L, Van Camp G, Smith RJ. Sundstrom RA, et al. Am J Med Genet. 1999 Sep 24;89(3):123-9. doi: 10.1002/(sici)1096-8628(19990924)89:3<123::aid-ajmg2>3.0.co;2-p. Am J Med Genet. 1999. PMID: 10704186 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.
Genetics of hearing impairment.
Hone SW, Smith RJ. Hone SW, et al. Semin Neonatol. 2001 Dec;6(6):531-41. doi: 10.1053/siny.2001.0094. Semin Neonatol. 2001. PMID: 12014894 Review.
Genotype-phenotype correlations for SLC26A4-related deafness.
Azaiez H, Yang T, Prasad S, Sorensen JL, Nishimura CJ, Kimberling WJ, Smith RJ. Azaiez H, et al. Hum Genet. 2007 Dec;122(5):451-7. doi: 10.1007/s00439-007-0415-2. Epub 2007 Aug 10. Hum Genet. 2007. PMID: 17690912 Free PMC article.
41 results