PubMed for id: 321902

Year	Number of Results
1994	1
1997	1
1998	6
1999	4
2000	2
2002	4
2004	4
2006	4
2007	5
2008	4
2009	2
2010	3
2011	2
2012	3
2013	2
2014	6
2015	2
2016	2
2017	2
2019	4
2020	3
2021	5
2022	2
2023	1
2024	0

1

Identification of a Novel TECTA mutation in a Chinese DFNA8/12 family with prelingual progressive sensorineural hearing impairment.

Li Z, Guo Y, Lu Y, Li J, Jin Z, Li H, Lu Y, Dai P, Han D, Cheng J, Yuan H. Li Z, et al. PLoS One. 2013 Jul 31;8(7):e70134. doi: 10.1371/journal.pone.0070134. Print 2013. PLoS One. 2013. PMID: 23936151 Free PMC article.

2

DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

Hildebrand MS, Morín M, Meyer NC, Mayo F, Modamio-Hoybjor S, Mencía A, Olavarrieta L, Morales-Angulo C, Nishimura CJ, Workman H, DeLuca AP, del Castillo I, Taylor KR, Tompkins B, Goodman CW, Schrauwen I, Wesemael MV, Lachlan K, Shearer AE, Braun TA, Huygen PL, Kremer H, Van Camp G, Moreno F, Casavant TL, Smith RJ, Moreno-Pelayo MA. Hildebrand MS, et al. Hum Mutat. 2011 Jul;32(7):825-34. doi: 10.1002/humu.21512. Epub 2011 Jun 7. Hum Mutat. 2011. PMID: 21520338 Free PMC article.

3

Flat threshold and mid-frequency hearing impairment in a Dutch DFNA8/12 family with a novel mutation in TECTA. Some evidence for protection of the inner ear.

de Heer AR, Pauw RJ, Huygen PL, Collin RW, Kremer H, Cremers CW. de Heer AR, et al. Audiol Neurootol. 2009;14(3):153-62. doi: 10.1159/000171477. Epub 2008 Nov 13. Audiol Neurootol. 2009. PMID: 19005249

4

Mid-frequency DFNA8/12 hearing loss caused by a synonymous TECTA mutation that affects an exonic splice enhancer.

Collin RW, de Heer AM, Oostrik J, Pauw RJ, Plantinga RF, Huygen PL, Admiraal R, de Brouwer AP, Strom TM, Cremers CW, Kremer H. Collin RW, et al. Eur J Hum Genet. 2008 Dec;16(12):1430-6. doi: 10.1038/ejhg.2008.110. Epub 2008 Jun 25. Eur J Hum Genet. 2008. PMID: 18575463

5

[From gene to disease; DFNA8/12, an autosomal dominant inherited bowl-shaped sensorineural hearing impairment].

Cremers CW, Plantinga RF, Kremer H. Cremers CW, et al. Ned Tijdschr Geneeskd. 2007 Mar 3;151(9):531-4. Ned Tijdschr Geneeskd. 2007. PMID: 17373394 Review. Dutch.

6

Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.

Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ. Plantinga RF, et al. J Assoc Res Otolaryngol. 2007 Mar;8(1):1-7. doi: 10.1007/s10162-006-0060-9. Epub 2006 Nov 30. J Assoc Res Otolaryngol. 2007. PMID: 17136632 Free PMC article.

7

A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation.

Plantinga RF, de Brouwer AP, Huygen PL, Kunst HP, Kremer H, Cremers CW. Plantinga RF, et al. J Assoc Res Otolaryngol. 2006 Jun;7(2):173-81. doi: 10.1007/s10162-006-0033-z. Epub 2006 Apr 25. J Assoc Res Otolaryngol. 2006. PMID: 16718611 Free PMC article.

8

A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.

Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE. Govaerts PJ, et al. Am J Otol. 1998 Nov;19(6):718-23. Am J Otol. 1998. PMID: 9831143

9

Autosomal-dominant, prelingual, nonprogressive sensorineural hearing loss: localization of the gene (DFNA8) to chromosome 11q by linkage in an Austrian family.

Kirschhofer K, Kenyon JB, Hoover DM, Franz P, Weipoltshammer K, Wachtler F, Kimberling WJ. Kirschhofer K, et al. Cytogenet Cell Genet. 1998;82(1-2):126-30. doi: 10.1159/000015086. Cytogenet Cell Genet. 1998. PMID: 9763681

10

A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.

Verhoeven K, Van Camp G, Govaerts PJ, Balemans W, Schatteman I, Verstreken M, Van Laer L, Smith RJ, Brown MR, Van de Heyning PH, Somers T, Offeciers FE, Willems PJ. Verhoeven K, et al. Am J Hum Genet. 1997 May;60(5):1168-73. Am J Hum Genet. 1997. PMID: 9150164 Free PMC article.

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