PubMed for id: 330838

Year	Number of Results
2003	2
2005	2
2006	1
2010	2
2011	2
2013	2
2017	3
2018	1
2019	2
2023	2
2024	0

1

Monogenic Causes of Low-Frequency Non-Syndromic Hearing Loss.

Gan NS, Oziębło D, Skarżyński H, Ołdak M. Gan NS, et al. Audiol Neurootol. 2023;28(5):327-337. doi: 10.1159/000529464. Epub 2023 Apr 28. Audiol Neurootol. 2023. PMID: 37121227 Free article. Review.

2

WFS1 autosomal dominant variants linked with hearing loss: update on structural analysis and cochlear implant outcome.

Lim HD, Lee SM, Yun YJ, Lee DH, Lee JH, Oh SH, Lee SY. Lim HD, et al. BMC Med Genomics. 2023 Apr 11;16(1):79. doi: 10.1186/s12920-023-01506-x. BMC Med Genomics. 2023. PMID: 37041640 Free PMC article.

3

Unique Mutational Spectrum of the GJB2 Gene and its Pathogenic Contribution to Deafness in Tuvinians (Southern Siberia, Russia): A High Prevalence of Rare Variant c.516G>C (p.Trp172Cys).

Posukh OL, Zytsar MV, Bady-Khoo MS, Danilchenko VY, Maslova EA, Barashkov NA, Bondar AA, Morozov IV, Maximov VN, Voevoda MI. Posukh OL, et al. Genes (Basel). 2019 Jun 5;10(6):429. doi: 10.3390/genes10060429. Genes (Basel). 2019. PMID: 31195736 Free PMC article.

4

Targeted Mutation Analysis of the SLC26A4, MYO6, PJVK and CDH23 Genes in Iranian Patients with AR Nonsyndromic Hearing Loss.

Alimardani M, Hosseini SM, Khaniani MS, Haghi MR, Eslahi A, Farjami M, Chezgi J, Derakhshan SM, Mojarrad M. Alimardani M, et al. Fetal Pediatr Pathol. 2019 Apr;38(2):93-102. doi: 10.1080/15513815.2018.1547336. Epub 2018 Dec 23. Fetal Pediatr Pathol. 2019. PMID: 30582396

5

Hearing Preservation During Cochlear Implantation and Electroacoustic Stimulation in Patients With SLC26A4 Mutations.

Roh KJ, Park S, Jung JS, Moon IS, Kim SH, Bang MY, Choi JY. Roh KJ, et al. Otol Neurotol. 2017 Oct;38(9):1262-1267. doi: 10.1097/MAO.0000000000001522. Otol Neurotol. 2017. PMID: 28796087

6

New role of LRP5, associated with nonsyndromic autosomal-recessive hereditary hearing loss.

Xia W, Hu J, Liu F, Ma J, Sun S, Zhang J, Jin K, Huang J, Jiang N, Wang X, Li W, Ma Z, Ma D. Xia W, et al. Hum Mutat. 2017 Oct;38(10):1421-1431. doi: 10.1002/humu.23285. Epub 2017 Aug 1. Hum Mutat. 2017. PMID: 28677207

7

[Mutation analysis and prenatal diagnosis for 12 families affected with hereditary hearing loss and enlarged vestibular aqueduct].

Xiang Y, Li H, Xu X, Xu C, Chen C, Lin X, Tang S. Xiang Y, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017 Jun 10;34(3):336-341. doi: 10.3760/cma.j.issn.1003-9406.2017.03.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2017. PMID: 28604950 Chinese.

8

Hair phenotype in non-syndromic deafness.

Volo T, Sathiyaseelan T, Astolfi L, Guaran V, Trevisi P, Emanuelli E, Martini A. Volo T, et al. Int J Pediatr Otorhinolaryngol. 2013 Aug;77(8):1280-5. doi: 10.1016/j.ijporl.2013.05.010. Epub 2013 Jun 14. Int J Pediatr Otorhinolaryngol. 2013. PMID: 23751281

9

Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.

Riahi Z, Hammami H, Ouragini H, Messai H, Zainine R, Bouyacoub Y, Romdhane L, Essaid D, Kefi R, Rhimi M, Bedoui M, Dhaouadi A, Feldmann D, Jonard L, Besbes G, Abdelhak S. Riahi Z, et al. Gene. 2013 Aug 1;525(1):1-4. doi: 10.1016/j.gene.2013.04.078. Epub 2013 May 13. Gene. 2013. PMID: 23680645

10

Vestibular dysfunction in DFNB1 deafness.

Dodson KM, Blanton SH, Welch KO, Norris VW, Nuzzo RL, Wegelin JA, Marin RS, Nance WE, Pandya A, Arnos KS. Dodson KM, et al. Am J Med Genet A. 2011 May;155A(5):993-1000. doi: 10.1002/ajmg.a.33828. Epub 2011 Apr 4. Am J Med Genet A. 2011. PMID: 21465647 Free PMC article.

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

17 results

Results by year