PubMed for id: 321966

Year	Number of Results
1996	1
1998	2
2000	5
2001	2
2002	1
2004	2
2006	1
2007	4
2011	2
2012	1
2013	1
2014	2
2015	7
2016	3
2017	3
2018	1
2019	1
2020	3
2021	3
2022	2
2024	0

1

Audiometric Characteristics of a Dutch DFNA10 Family With Mid-Frequency Hearing Impairment.

van Beelen E, Oonk AM, Leijendeckers JM, Hoefsloot EH, Pennings RJ, Feenstra I, Dieker HJ, Huygen PL, Snik AF, Kremer H, Kunst HP. van Beelen E, et al. Ear Hear. 2016 Jan-Feb;37(1):103-11. doi: 10.1097/AUD.0000000000000217. Ear Hear. 2016. PMID: 26331839

2

A novel splice site mutation in EYA4 causes DFNA10 hearing loss.

Hildebrand MS, Coman D, Yang T, Gardner RJ, Rose E, Smith RJ, Bahlo M, Dahl HH. Hildebrand MS, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1599-604. doi: 10.1002/ajmg.a.31860. Am J Med Genet A. 2007. PMID: 17568404

3

Nonsyndromic hearing loss DFNA10 and a novel mutation of EYA4: evidence for correlation of normal cardiac phenotype with truncating mutations of the Eya domain.

Makishima T, Madeo AC, Brewer CC, Zalewski CK, Butman JA, Sachdev V, Arai AE, Holbrook BM, Rosing DR, Griffith AJ. Makishima T, et al. Am J Med Genet A. 2007 Jul 15;143A(14):1592-8. doi: 10.1002/ajmg.a.31793. Am J Med Genet A. 2007. PMID: 17567890

4

A comparative study of Eya1 and Eya4 protein function and its implication in branchio-oto-renal syndrome and DFNA10.

Zhang Y, Knosp BM, Maconochie M, Friedman RA, Smith RJ. Zhang Y, et al. J Assoc Res Otolaryngol. 2004 Sep;5(3):295-304. doi: 10.1007/s10162-004-4044-3. Epub 2004 Jun 24. J Assoc Res Otolaryngol. 2004. PMID: 15492887 Free PMC article.

5

A 4-bp insertion in the eya-homologous region (eyaHR) of EYA4 causes hearing impairment in a Hungarian family linked to DFNA10.

Pfister M, Tóth T, Thiele H, Haack B, Blin N, Zenner HP, Sziklai I, Nürnberg P, Kupka S. Pfister M, et al. Mol Med. 2002 Oct;8(10):607-11. Mol Med. 2002. PMID: 12477971 Free PMC article.

6

The DFNA10 phenotype.

De Leenheer EM, Huygen PL, Wayne S, Smith RJ, Cremers CW. De Leenheer EM, et al. Ann Otol Rhinol Laryngol. 2001 Sep;110(9):861-6. doi: 10.1177/000348940111000910. Ann Otol Rhinol Laryngol. 2001. PMID: 11558763

7

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

8

Audiometric analysis of a Belgian family linked to the DFNA10 locus.

Verstreken M, Declau F, Schatteman I, Van Velzen D, Verhoeven K, Van Camp G, Willems PJ, Kuhweide EW, Verhaert E, D'Haese P, Wuyts FL, Van de Heyning PH. Verstreken M, et al. Am J Otol. 2000 Sep;21(5):675-81. Am J Otol. 2000. PMID: 10993457

9

Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.

Verhoeven K, Fagerheim T, Prasad S, Wayne S, De Clau F, Balemans W, Verstreken M, Schatteman I, Solem B, Van de Heyning P, Tranebjärg L, Smith RJ, Van Camp G. Verhoeven K, et al. Hum Genet. 2000 Jul;107(1):7-11. doi: 10.1007/s004390000319. Hum Genet. 2000. PMID: 10982027

10

A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6.

O'Neill ME, Marietta J, Nishimura D, Wayne S, Van Camp G, Van Laer L, Negrini C, Wilcox ER, Chen A, Fukushima K, Ni L, Sheffield VC, Smith RJ. O'Neill ME, et al. Hum Mol Genet. 1996 Jun;5(6):853-6. doi: 10.1093/hmg/5.6.853. Hum Mol Genet. 1996. PMID: 8776603

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

45 results

Results by year