256 related articles for article (PubMed ID: 30473558)
1. 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]
2. 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]
3. 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]
4. Novel compound heterozygous mutations in SLC26A4 gene in a Chinese Han family with enlarged vestibular aqueduct.
Wang M; Zhang F; Xu L; Xiao Y; Li J; Fan Z; Sun Q; Bai X; Wang H
Int J Pediatr Otorhinolaryngol; 2016 Nov; 90():170-174. PubMed ID: 27729126
[TBL] [Abstract][Full Text] [Related]
5. A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.
Liang Y; Peng Q; Wang K; Zhu P; Wu C; Rao C; Chang J; Li S; Lu X
Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():97-100. PubMed ID: 29501320
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Mutational analysis of the SLC26A4 gene in Chinese sporadic nonsyndromic hearing-impaired children.
Hu X; Liang F; Zhao M; Gong A; Berry ER; Shi Y; Wang Y; Chen Y; Liu A; Qu C
Int J Pediatr Otorhinolaryngol; 2012 Oct; 76(10):1474-80. PubMed ID: 22796198
[TBL] [Abstract][Full Text] [Related]
8. A newly identified mutation (c.2029 C > T) in SLC26A4 gene is associated with enlarged vestibular aqueducts in a Chinese family.
Wu T; Cui L; Mou Y; Guo W; Liu D; Qiu J; Xu C; Zhou J; Han F; Sun Y
BMC Med Genomics; 2022 Mar; 15(1):49. PubMed ID: 35249537
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Extremely discrepant mutation spectrum of SLC26A4 between Chinese patients with isolated Mondini deformity and enlarged vestibular aqueduct.
Huang S; Han D; Yuan Y; Wang G; Kang D; Zhang X; Yan X; Meng X; Dong M; Dai P
J Transl Med; 2011 Sep; 9():167. PubMed ID: 21961810
[TBL] [Abstract][Full Text] [Related]
11. [Genotype and clinical phenotype analysis of 42 patients with delayed nonsyndromic hearing loss].
Niu W; Xu H; Qin L; Wang G; Ding S; Xie C; Jia X; Liu H
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Feb; 35(2):131-136. PubMed ID: 33540994
[No Abstract] [Full Text] [Related]
12. 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]
13. [Sequencing analysis of whole SLC26A4 gene related to IVS7-2A > G mutation in 1552 moderate to profound sensorineural hearing loss patients in China].
Yuan YY; Dai P; Zhu QW; Kang DY; Huang DL
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Jun; 44(6):449-54. PubMed ID: 19954013
[TBL] [Abstract][Full Text] [Related]
14. SLC26A4-linked CEVA haplotype correlates with phenotype in patients with enlargement of the vestibular aqueduct.
Chao JR; Chattaraj P; Munjal T; Honda K; King KA; Zalewski CK; Chien WW; Brewer CC; Griffith AJ
BMC Med Genet; 2019 Jul; 20(1):118. PubMed ID: 31266487
[TBL] [Abstract][Full Text] [Related]
15. [Analysis of genotypes on 850 newborns with
Huang LH; Zhao XL; Cheng XH; Yu YD; Wen C; Li Y; Wang XL; Wang XY; Ruan Y; En H
Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2023 Feb; 58(2):117-125. PubMed ID: 36748152
[No Abstract] [Full Text] [Related]
16. 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]
17. Identification of two heterozygous deafness mutations in SLC26A4 (PDS) in a Chinese family with two siblings.
Chen J; Wei Q; Yao J; Qian X; Dai Y; Yang Y; Cao X; Gao X
Int J Audiol; 2013 Feb; 52(2):134-8. PubMed ID: 23151031
[TBL] [Abstract][Full Text] [Related]
18. A novel SLC26A4 splicing mutation identified in two deaf Chinese twin sisters with enlarged vestibular aqueducts.
Zhou K; Huang L; Feng M; Li X; Zhao Y; Liu F; Wei J; Qin D; Lu Q; Shi M; Qu S; Tang F
Mol Genet Genomic Med; 2020 Oct; 8(10):e1447. PubMed ID: 32770655
[TBL] [Abstract][Full Text] [Related]
19. Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct.
Yao G; Li S; Chen D; Wang H; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
Int J Pediatr Otorhinolaryngol; 2013 Apr; 77(4):544-9. PubMed ID: 23385134
[TBL] [Abstract][Full Text] [Related]
20. Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.
Dai P; Stewart AK; Chebib F; Hsu A; Rozenfeld J; Huang D; Kang D; Lip V; Fang H; Shao H; Liu X; Yu F; Yuan H; Kenna M; Miller DT; Shen Y; Yang W; Zelikovic I; Platt OS; Han D; Alper SL; Wu BL
Physiol Genomics; 2009 Aug; 38(3):281-90. PubMed ID: 19509082
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]