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Page 1
High frequency hearing loss correlated with mutations in the GJB2 gene.
Hum Genet. 2000 Apr;106(4):399-405. doi: 10.1007/s004390000273.
Hum Genet. 2000.
PMID: 10830906
Prevalence and nature of connexin 26 mutations in children with non-syndromic deafness.
Dahl HH, Saunders K, Kelly TM, Osborn AH, Wilcox S, Cone-Wesson B, Wunderlich JL, Du Sart D, Kamarinos M, Gardner RJ, Dennehy S, Williamson R, Vallance N, Mutton P.
Dahl HH, et al. Among authors: kamarinos m.
Med J Aust. 2001 Aug 20;175(4):191-4. doi: 10.5694/j.1326-5377.2001.tb143093.x.
Med J Aust. 2001.
PMID: 11587277
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Identification of a novel COCH mutation, I109N, highlights the similar clinical features observed in DFNA9 families.
Kamarinos M, McGill J, Lynch M, Dahl H.
Kamarinos M, et al.
Hum Mutat. 2001 Apr;17(4):351. doi: 10.1002/humu.37.
Hum Mutat. 2001.
PMID: 11295836
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