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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1996 1
1997 3
1998 1
1999 2
2000 3
2001 5
2002 6
2003 2
2004 2
2005 4
2006 2
2007 6
2008 4
2009 3
2010 2
2011 5
2012 5
2013 2
2014 4
2015 3
2016 5
2017 1
2018 2
2019 7
2020 1
2021 3
2022 4
2023 5
2024 0

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PubMed for id: 388720

87 results

Results by year

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Page 1
A common founder effect of the splice site variant c.-23 + 1G > A in GJB2 gene causing autosomal recessive deafness 1A (DFNB1A) in Eurasia.
Solovyev AV, Kushniarevich A, Bliznetz E, Bady-Khoo M, Lalayants MR, Markova TG, Minárik G, Kádasi L, Metspalu E, Pshennikova VG, Teryutin FM, Khusnutdinova EK, Poliakov A, Metspalu M, Posukh OL, Barashkov NA, Fedorova SA. Solovyev AV, et al. Hum Genet. 2022 Apr;141(3-4):697-707. doi: 10.1007/s00439-021-02405-w. Epub 2021 Nov 27. Hum Genet. 2022. PMID: 34839402
Comparison of Predictive In Silico Tools on Missense Variants in GJB2, GJB6, and GJB3 Genes Associated with Autosomal Recessive Deafness 1A (DFNB1A).
Pshennikova VG, Barashkov NA, Romanov GP, Teryutin FM, Solov'ev AV, Gotovtsev NN, Nikanorova AA, Nakhodkin SS, Sazonov NN, Morozov IV, Bondar AA, Dzhemileva LU, Khusnutdinova EK, Posukh OL, Fedorova SA. Pshennikova VG, et al. ScientificWorldJournal. 2019 Mar 20;2019:5198931. doi: 10.1155/2019/5198931. eCollection 2019. ScientificWorldJournal. 2019. PMID: 31015822 Free PMC article.
Connexin 26 deafness is not always congenital.
Orzan E, Murgia A. Orzan E, et al. Int J Pediatr Otorhinolaryngol. 2007 Mar;71(3):501-7. doi: 10.1016/j.ijporl.2006.12.002. Epub 2007 Jan 11. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17222463
Audiological features of GJB2 (connexin 26) deafness.
Liu XZ, Pandya A, Angeli S, Telischi FF, Arnos KS, Nance WE, Balkany T. Liu XZ, et al. Ear Hear. 2005 Jun;26(3):361-9. doi: 10.1097/00003446-200506000-00011. Ear Hear. 2005. PMID: 15937416
A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
Cryns K, Orzan E, Murgia A, Huygen PL, Moreno F, del Castillo I, Chamberlin GP, Azaiez H, Prasad S, Cucci RA, Leonardi E, Snoeckx RL, Govaerts PJ, Van de Heyning PH, Van de Heyning CM, Smith RJ, Van Camp G. Cryns K, et al. J Med Genet. 2004 Mar;41(3):147-54. doi: 10.1136/jmg.2003.013896. J Med Genet. 2004. PMID: 14985372 Free PMC article.
87 results