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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2002 | 1 |
2009 | 1 |
2010 | 1 |
2012 | 1 |
2014 | 1 |
2024 | 0 |
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Page 1
Unique spectrum of GJB2 mutations in Mexico.
Int J Pediatr Otorhinolaryngol. 2012 Nov;76(11):1678-80. doi: 10.1016/j.ijporl.2012.08.005. Epub 2012 Aug 24.
Int J Pediatr Otorhinolaryngol. 2012.
PMID: 22925408
Frequency of GJB2 and del(GJB6-D13S1830) mutations among an Ecuadorian mestizo population.
Paz-y-Miño C, Beaty D, López-Cortés A, Proaño I.
Paz-y-Miño C, et al.
Int J Pediatr Otorhinolaryngol. 2014 Oct;78(10):1648-54. doi: 10.1016/j.ijporl.2014.07.014. Epub 2014 Jul 21.
Int J Pediatr Otorhinolaryngol. 2014.
PMID: 25085072
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High frequency of connexin26 (GJB2) mutations associated with nonsyndromic hearing loss in the population of Kerala, India.
Joseph AY, Rasool TJ.
Joseph AY, et al.
Int J Pediatr Otorhinolaryngol. 2009 Mar;73(3):437-43. doi: 10.1016/j.ijporl.2008.11.010. Epub 2009 Jan 20.
Int J Pediatr Otorhinolaryngol. 2009.
PMID: 19157576
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Connexin-26-associated deafness: phenotypic variability and progression of hearing loss.
Chan DK, Schrijver I, Chang KW.
Chan DK, et al.
Genet Med. 2010 Mar;12(3):174-81. doi: 10.1097/GIM.0b013e3181d0d42b.
Genet Med. 2010.
PMID: 20154630
Free article.
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Effectiveness of sequencing connexin 26 (GJB2) in cases of familial or sporadic childhood deafness referred for molecular diagnostic testing.
Wu BL, Lindeman N, Lip V, Adams A, Amato RS, Cox G, Irons M, Kenna M, Korf B, Raisen J, Platt O.
Wu BL, et al.
Genet Med. 2002 Jul-Aug;4(4):279-88. doi: 10.1097/00125817-200207000-00006.
Genet Med. 2002.
PMID: 12172394
Free article.
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