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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
1997 | 2 |
2000 | 1 |
2002 | 3 |
2009 | 1 |
2024 | 0 |
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7 results
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Page 1
Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.
Hum Mol Genet. 1997 Sep;6(9):1605-9. doi: 10.1093/hmg/6.9.1605.
Hum Mol Genet. 1997.
PMID: 9285800
Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
Carrasquillo MM, Zlotogora J, Barges S, Chakravarti A.
Carrasquillo MM, et al.
Hum Mol Genet. 1997 Nov;6(12):2163-72. doi: 10.1093/hmg/6.12.2163.
Hum Mol Genet. 1997.
PMID: 9328482
Item in Clipboard
Exploring the clinical and epidemiological complexity of GJB2-linked deafness.
Gualandi F, Ravani A, Berto A, Sensi A, Trabanelli C, Falciano F, Trevisi P, Mazzoli M, Tibiletti MG, Cristofari E, Burdo S, Ferlini A, Martini A, Calzolari E.
Gualandi F, et al.
Am J Med Genet. 2002 Sep 15;112(1):38-45. doi: 10.1002/ajmg.10621.
Am J Med Genet. 2002.
PMID: 12239718
Item in Clipboard
Connexin 26: required for normal auditory function.
Kelley PM, Cohn E, Kimberling WJ.
Kelley PM, et al.
Brain Res Brain Res Rev. 2000 Apr;32(1):184-8. doi: 10.1016/s0165-0173(99)00080-6.
Brain Res Brain Res Rev. 2000.
PMID: 10751669
Review.
Item in Clipboard
GJB2 (connexin 26) variants and nonsyndromic sensorineural hearing loss: a HuGE review.
Kenneson A, Van Naarden Braun K, Boyle C.
Kenneson A, et al.
Genet Med. 2002 Jul-Aug;4(4):258-74. doi: 10.1097/00125817-200207000-00004.
Genet Med. 2002.
PMID: 12172392
Free article.
Review.
Item in Clipboard
Hearing loss: frequency and functional studies of the most common connexin26 alleles.
D'Andrea P, Veronesi V, Bicego M, Melchionda S, Zelante L, Di Iorio E, Bruzzone R, Gasparini P.
D'Andrea P, et al.
Biochem Biophys Res Commun. 2002 Aug 23;296(3):685-91. doi: 10.1016/s0006-291x(02)00891-4.
Biochem Biophys Res Commun. 2002.
PMID: 12176036
Item in Clipboard
Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency.
Mahdieh N, Rabbani B.
Mahdieh N, et al.
Int J Audiol. 2009;48(6):363-70. doi: 10.1080/14992020802607449.
Int J Audiol. 2009.
PMID: 19925344
Review.
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