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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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1999 | 2 |
2001 | 1 |
2002 | 1 |
2024 | 0 |
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Page 1
The phenotype of DFNA13/COL11A2.
Adv Otorhinolaryngol. 2002;61:85-91. doi: 10.1159/000066804.
Adv Otorhinolaryngol. 2002.
PMID: 12408068
No abstract available.
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
Wayne S, Robertson NG, DeClau F, Chen N, Verhoeven K, Prasad S, Tranebjärg L, Morton CC, Ryan AF, Van Camp G, Smith RJ.
Wayne S, et al.
Hum Mol Genet. 2001 Feb 1;10(3):195-200. doi: 10.1093/hmg/10.3.195.
Hum Mol Genet. 2001.
PMID: 11159937
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Connexin 26 as a cause of hereditary hearing loss.
McGuirt WT, Smith RJ.
McGuirt WT, et al.
Am J Audiol. 1999 Dec;8(2):93-100. doi: 10.1044/1059-0889(1999/016).
Am J Audiol. 1999.
PMID: 10646192
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Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13).
McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C, Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW, Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ.
McGuirt WT, et al.
Nat Genet. 1999 Dec;23(4):413-9. doi: 10.1038/70516.
Nat Genet. 1999.
PMID: 10581026
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