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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2000 | 1 |
2002 | 1 |
2006 | 1 |
2009 | 1 |
2010 | 2 |
2013 | 2 |
2024 | 0 |
Search Results
7 results
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Page 1
Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
Hum Mutat. 2000 Dec;16(6):502-8. doi: 10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4.
Hum Mutat. 2000.
PMID: 11102979
Performance of cochlear implant recipients with GJB2-related deafness.
Green GE, Scott DA, McDonald JM, Teagle HF, Tomblin BJ, Spencer LJ, Woodworth GG, Knutson JF, Gantz BJ, Sheffield VC, Smith RJ.
Green GE, et al.
Am J Med Genet. 2002 May 1;109(3):167-70. doi: 10.1002/ajmg.10330.
Am J Med Genet. 2002.
PMID: 11977173
Free PMC article.
Item in Clipboard
Temporal bone imaging in GJB2 deafness.
Propst EJ, Blaser S, Stockley TL, Harrison RV, Gordon KA, Papsin BC.
Propst EJ, et al.
Laryngoscope. 2006 Dec;116(12):2178-86. doi: 10.1097/01.mlg.0000244389.68568.a7.
Laryngoscope. 2006.
PMID: 17146393
Clinical Trial.
Item in Clipboard
Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
Gravina LP, Foncuberta ME, Prieto ME, Garrido J, Barreiro C, Chertkoff L.
Gravina LP, et al.
Int J Pediatr Otorhinolaryngol. 2010 Mar;74(3):250-4. doi: 10.1016/j.ijporl.2009.11.014. Epub 2009 Dec 22.
Int J Pediatr Otorhinolaryngol. 2010.
PMID: 20022641
Item in Clipboard
Causes of hearing impairment in the Norwegian paediatric cochlear implant program.
Siem G, Fagerheim T, Jonsrud C, Laurent C, Teig E, Harris S, Leren TP, Früh A, Heimdal K.
Siem G, et al.
Int J Audiol. 2010 Aug;49(8):596-605. doi: 10.3109/14992021003743269.
Int J Audiol. 2010.
PMID: 20553101
Item in Clipboard
Etiology and audiological outcomes at 3 years for 364 children in Australia.
Dahl HH, Ching TY, Hutchison W, Hou S, Seeto M, Sjahalam-King J.
Dahl HH, et al.
PLoS One. 2013;8(3):e59624. doi: 10.1371/journal.pone.0059624. Epub 2013 Mar 28.
PLoS One. 2013.
PMID: 23555729
Free PMC article.
Item in Clipboard
Identification of four novel connexin 26 mutations in non-syndromic deaf patients: genotype-phenotype analysis in moderate cases.
Dalamón V, Florencia Wernert M, Lotersztein V, Craig PO, Diamante RR, Barteik ME, Curet C, Paoli B, Mansilla E, Elgoyhen AB.
Dalamón V, et al.
Mol Biol Rep. 2013 Dec;40(12):6945-55. doi: 10.1007/s11033-013-2814-x. Epub 2013 Oct 25.
Mol Biol Rep. 2013.
PMID: 24158611
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