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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1997 | 1 |
1998 | 1 |
2012 | 1 |
2013 | 1 |
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2015 | 1 |
2024 | 0 |
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Page 1
Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.
Nature. 1997 May 1;387(6628):80-3. doi: 10.1038/387080a0.
Nature. 1997.
PMID: 9139825
High incidence of GJB2 gene mutations among assortatively mating hearing impaired families in Kerala: future implications.
Pavithra A, Jeffrey JM, Chandru J, Ramesh A, Srisailapathy CR.
Pavithra A, et al.
J Genet. 2014 Apr;93(1):207-13. doi: 10.1007/s12041-014-0338-3.
J Genet. 2014.
PMID: 24840842
Free article.
No abstract available.
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Mutations of GJB2 encoding connexin 26 contribute to non-syndromic moderate and severe hearing loss in Pakistan.
Salman M, Bashir R, Imtiaz A, Maqsood A, Mujtaba G, Iqbal M, Naz S.
Salman M, et al.
Eur Arch Otorhinolaryngol. 2015 Aug;272(8):2071-5. doi: 10.1007/s00405-015-3523-y. Epub 2015 Jan 31.
Eur Arch Otorhinolaryngol. 2015.
PMID: 25636251
Free PMC article.
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Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
Kelley PM, Harris DJ, Comer BC, Askew JW, Fowler T, Smith SD, Kimberling WJ.
Kelley PM, et al.
Am J Hum Genet. 1998 Apr;62(4):792-9. doi: 10.1086/301807.
Am J Hum Genet. 1998.
PMID: 9529365
Free PMC article.
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A novel p.Leu213X mutation in GJB2 gene in a Portuguese family.
Gonçalves AC, Chora J, Matos TD, Santos R, O'Neill A, Escada P, Fialho G, Caria H.
Gonçalves AC, et al.
Int J Pediatr Otorhinolaryngol. 2013 Jan;77(1):89-91. doi: 10.1016/j.ijporl.2012.10.002. Epub 2012 Nov 8.
Int J Pediatr Otorhinolaryngol. 2013.
PMID: 23141775
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