104 related articles for article (PubMed ID: 30086623)
1. Two Compound Heterozygous Were Identified in SLC26A4 Gene in Two Chinese Families With Enlarged Vestibular Aqueduct.
Yu Y; Yang Y; Lu J; Jin Y; Yang Y; Hong E; Shi J; Chen F; Han S; Chu P; Guo Y; Ni X
Clin Exp Otorhinolaryngol; 2019 Feb; 12(1):50-57. PubMed ID: 30086623
[TBL] [Abstract][Full Text] [Related]
2. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct.
Zhao X; Cheng X; Huang L; Wang X; Wen C; Wang X
Biosci Trends; 2018; 12(5):502-506. PubMed ID: 30473558
[TBL] [Abstract][Full Text] [Related]
3. Identification of a novel mutation in SLC26A4 gene in a Chinese family with enlarged vestibular aqueduct syndrome.
Zhang F; Bai X; Xiao Y; Zhang X; Zhang G; Li J; Xu L; Wang H
Int J Pediatr Otorhinolaryngol; 2016 Jun; 85():75-9. PubMed ID: 27240500
[TBL] [Abstract][Full Text] [Related]
4. A novel missense mutation in the SLC26A4 gene causes nonsyndromic hearing loss and enlarged vestibular aqueduct.
He X; Peng Q; Li S; Zhu P; Wu C; Rao C; Chang J; Xie M; Zhong B; Lu X
Int J Pediatr Otorhinolaryngol; 2017 Apr; 95():104-108. PubMed ID: 28576516
[TBL] [Abstract][Full Text] [Related]
5. Mutation analysis of the SLC26A4 gene in three Chinese families.
Wen C; Wang S; Zhao X; Wang X; Wang X; Cheng X; Huang L
Biosci Trends; 2019 Nov; 13(5):441-447. PubMed ID: 31656273
[TBL] [Abstract][Full Text] [Related]
6. A novel compound heterozygous mutation of SLC26A4 in two Chinese families with nonsyndromic hearing loss and enlarged vestibular aqueducts.
Zhu GJ; Shi LS; Zhou H; Yang Y; Chen J; Gao X
Mol Med Rep; 2017 Dec; 16(6):9011-9016. PubMed ID: 28990112
[TBL] [Abstract][Full Text] [Related]
7. Compound heterozygous variants of the SLC26A4 gene in a Chinese family with enlarged vestibular aqueducts.
He X; Zhao S; Shi L; Lu Y; Yang Y; Zhang X
BMC Med Genomics; 2022 Jul; 15(1):152. PubMed ID: 35804348
[TBL] [Abstract][Full Text] [Related]
8. Mono-allelic mutations of SLC26A4 is over-presented in deaf patients with non-syndromic enlarged vestibular aqueduct.
Pang X; Chai Y; Chen P; He L; Wang X; Wu H; Yang T
Int J Pediatr Otorhinolaryngol; 2015 Aug; 79(8):1351-3. PubMed ID: 26100058
[TBL] [Abstract][Full Text] [Related]
9. Identification of novel functional null allele of SLC26A4 associated with enlarged vestibular aqueduct and its possible implication.
Jang JH; Jung J; Kim AR; Cho YM; Kim MY; Lee SY; Choi JY; Lee JH; Choi BY
Audiol Neurootol; 2014; 19(5):319-26. PubMed ID: 25358692
[TBL] [Abstract][Full Text] [Related]
10. Non-syndromic enlarged vestibular aqueduct caused by novel compound mutations of the
Huang Y; Li L; Pan L; Ling X; Wang C; Huang C; Huang Y
Front Genet; 2023; 14():1240701. PubMed ID: 37745850
[TBL] [Abstract][Full Text] [Related]
11. Mutations in the SLC26A4 (pendrin) gene in patients with sensorineural deafness and enlarged vestibular aqueduct.
Bogazzi F; Russo D; Raggi F; Ultimieri F; Berrettini S; Forli F; Grasso L; Ceccarelli C; Mariotti S; Pinchera A; Bartalena L; Martino E
J Endocrinol Invest; 2004 May; 27(5):430-5. PubMed ID: 15279074
[TBL] [Abstract][Full Text] [Related]
12. Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian sample of hearing-impaired subjects.
Nonose RW; Lezirovitz K; de Mello Auricchio MTB; Batissoco AC; Yamamoto GL; Mingroni-Netto RC
BMC Med Genet; 2018 May; 19(1):73. PubMed ID: 29739340
[TBL] [Abstract][Full Text] [Related]
13. Enlarged vestibular aqueduct: Audiological and genetical features in children and adolescents.
Aimoni C; Ciorba A; Cerritelli L; Ceruti S; Skarżyński PH; Hatzopoulos S
Int J Pediatr Otorhinolaryngol; 2017 Oct; 101():254-258. PubMed ID: 28780189
[TBL] [Abstract][Full Text] [Related]
14. [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
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):336-341. PubMed ID: 28604950
[TBL] [Abstract][Full Text] [Related]
15. A 7666-bp genomic deletion is frequent in Chinese Han deaf patients with non-syndromic enlarged vestibular aqueduct but without bi-allelic SLC26A4 mutations.
Pang X; Chai Y; He L; Chen P; Wang X; Li L; Jia H; Wu H; Yang T
Int J Pediatr Otorhinolaryngol; 2015 Dec; 79(12):2248-52. PubMed ID: 26549381
[TBL] [Abstract][Full Text] [Related]
16. Subgroups of enlarged vestibular aqueduct in relation to SLC26A4 mutations and hearing loss.
Okamoto Y; Mutai H; Nakano A; Arimoto Y; Sugiuchi T; Masuda S; Morimoto N; Sakamoto H; Ogahara N; Takagi A; Taiji H; Kaga K; Ogawa K; Matsunaga T
Laryngoscope; 2014 Apr; 124(4):E134-40. PubMed ID: 24105851
[TBL] [Abstract][Full Text] [Related]
17. The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct.
Madden C; Halsted M; Meinzen-Derr J; Bardo D; Boston M; Arjmand E; Nishimura C; Yang T; Benton C; Das V; Smith R; Choo D; Greinwald J
Arch Otolaryngol Head Neck Surg; 2007 Feb; 133(2):162-8. PubMed ID: 17309986
[TBL] [Abstract][Full Text] [Related]
18. A novel SLC26A4 (PDS) deafness mutation retained in the endoplasmic reticulum.
Brownstein ZN; Dror AA; Gilony D; Migirov L; Hirschberg K; Avraham KB
Arch Otolaryngol Head Neck Surg; 2008 Apr; 134(4):403-7. PubMed ID: 18427006
[TBL] [Abstract][Full Text] [Related]
19. Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct.
Lin YH; Wu CC; Lin YH; Lu YC; Chen CS; Liu TC; Chen PL; Hsu CJ
J Mol Diagn; 2019 Jan; 21(1):138-148. PubMed ID: 30268946
[TBL] [Abstract][Full Text] [Related]
20. Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome.
Wu CC; Lu YC; Chen PJ; Yeh PL; Su YN; Hwu WL; Hsu CJ
Audiol Neurootol; 2010; 15(1):57-66. PubMed ID: 19648736
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
