259 related articles for article (PubMed ID: 30473558)
41. Genotyping and audiological characteristics of infants with a single-allele SLC26A4 mutation.
Zhao X; Huang L; Wang X; Wang X; Zhao L; Cheng X; Ruan Y
Int J Pediatr Otorhinolaryngol; 2019 Jan; 116():153-158. PubMed ID: 30554688
[TBL] [Abstract][Full Text] [Related]
42. 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]
43. [Correlation of temporal bone HRCT,
Zhao Z; Zhu Y; Fu Y; Jiang H
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2022 Oct; 36(10):736-740. PubMed ID: 36217650
[No Abstract] [Full Text] [Related]
44. 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]
45. Mutation analysis of common deafness-causing genes among 506 patients with nonsyndromic hearing loss from Wenzhou city, China.
Xiang YB; Tang SH; Li HZ; Xu CY; Chen C; Xu YZ; Ding LR; Xu XQ
Int J Pediatr Otorhinolaryngol; 2019 Jul; 122():185-190. PubMed ID: 31035178
[TBL] [Abstract][Full Text] [Related]
46. A Novel mutation in the SLC26A4 gene in a Chinese family with Pendred syndrome.
Huang CJ; Lei TH; Chang WL; Tu TY; Shiao AS; Chiu CY; Jap TS
Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1495-9. PubMed ID: 23838540
[TBL] [Abstract][Full Text] [Related]
47. Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: a unique SLC26A4 mutation spectrum.
Hu H; Wu L; Feng Y; Pan Q; Long Z; Li J; Dai H; Xia K; Liang D; Niikawa N; Xia J
J Hum Genet; 2007; 52(6):492-497. PubMed ID: 17443271
[TBL] [Abstract][Full Text] [Related]
48. Comprehensive molecular etiology analysis of nonsyndromic hearing impairment from typical areas in China.
Yuan Y; You Y; Huang D; Cui J; Wang Y; Wang Q; Yu F; Kang D; Yuan H; Han D; Dai P
J Transl Med; 2009 Sep; 7():79. PubMed ID: 19744334
[TBL] [Abstract][Full Text] [Related]
49. Diagnostic Value of SLC26A4 Mutation Status in Hereditary Hearing Loss With EVA: A PRISMA-Compliant Meta-Analysis.
Lu YJ; Yao J; Wei QJ; Xing GQ; Cao X
Medicine (Baltimore); 2015 Dec; 94(50):e2248. PubMed ID: 26683941
[TBL] [Abstract][Full Text] [Related]
50. Study on the relationship between the pathogenic mutations of SLC26A4 and CT phenotypes of inner ear in patient with sensorineural hearing loss.
Wu L; Liu Y; Wu J; Chen S; Tang S; Jiang Y; Dai P
Biosci Rep; 2019 Mar; 39(3):. PubMed ID: 30842343
[TBL] [Abstract][Full Text] [Related]
51. A distinct spectrum of SLC26A4 mutations in patients with enlarged vestibular aqueduct in China.
Wang QJ; Zhao YL; Rao SQ; Guo YF; Yuan H; Zong L; Guan J; Xu BC; Wang DY; Han MK; Lan L; Zhai SQ; Shen Y
Clin Genet; 2007 Sep; 72(3):245-54. PubMed ID: 17718863
[TBL] [Abstract][Full Text] [Related]
52. [Screening of common deafness gene mutations in 17 000 Chinese newborns from Chengdu based on microarray analysis].
Lyu K; Xiong Y; Yu H; Zou L; Ran L; Liu D; Yin Q; Xu Y; Fang X; Song Z; Huang L; Tan D; Zhang Z
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Oct; 31(5):547-52. PubMed ID: 25297577
[TBL] [Abstract][Full Text] [Related]
53. [Analysis of 59 cases of large vestibular aqueduct syndrome
Su D; Lou F; Huang R; Li X; Lin K; Li G; Ma J
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2023 Nov; 37(11):909-915. PubMed ID: 37905486
[No Abstract] [Full Text] [Related]
54. Increased diagnosis of enlarged vestibular aqueduct by multiplex PCR enrichment and next-generation sequencing of the SLC26A4 gene.
Tian Y; Xu H; Liu D; Zhang J; Yang Z; Zhang S; Liu H; Li R; Tian Y; Zeng B; Li T; Lin Q; Wang H; Li X; Lu W; Shi Y; Zhang Y; Zhang H; Jiang C; Xu Y; Chen B; Liu J; Tang W
Mol Genet Genomic Med; 2021 Aug; 9(8):e1734. PubMed ID: 34170635
[TBL] [Abstract][Full Text] [Related]
55. Analysis of SLC26A4, FOXI1, and KCNJ10 Gene Variants in Patients with Incomplete Partition of the Cochlea and Enlarged Vestibular Aqueduct (EVA) Anomalies.
Klarov LA; Pshennikova VG; Romanov GP; Cherdonova AM; Solovyev AV; Teryutin FM; Luginov NV; Kotlyarov PM; Barashkov NA
Int J Mol Sci; 2022 Dec; 23(23):. PubMed ID: 36499699
[TBL] [Abstract][Full Text] [Related]
56. A common
Chattaraj P; Munjal T; Honda K; Rendtorff ND; Ratay JS; Muskett JA; Risso DS; Roux I; Gertz EM; Schäffer AA; Friedman TB; Morell RJ; Tranebjærg L; Griffith AJ
J Med Genet; 2017 Oct; 54(10):665-673. PubMed ID: 28780564
[TBL] [Abstract][Full Text] [Related]
57. 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]
58. Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.
Honda K; Griffith AJ
Hum Genet; 2022 Apr; 141(3-4):455-464. PubMed ID: 34345941
[TBL] [Abstract][Full Text] [Related]
59. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations.
Albert S; Blons H; Jonard L; Feldmann D; Chauvin P; Loundon N; Sergent-Allaoui A; Houang M; Joannard A; Schmerber S; Delobel B; Leman J; Journel H; Catros H; Dollfus H; Eliot MM; David A; Calais C; Drouin-Garraud V; Obstoy MF; Tran Ba Huy P; Lacombe D; Duriez F; Francannet C; Bitoun P; Petit C; Garabédian EN; Couderc R; Marlin S; Denoyelle F
Eur J Hum Genet; 2006 Jun; 14(6):773-9. PubMed ID: 16570074
[TBL] [Abstract][Full Text] [Related]
60. Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China.
Chai Y; Huang Z; Tao Z; Li X; Li L; Li Y; Wu H; Yang T
Am J Med Genet A; 2013 Sep; 161A(9):2226-33. PubMed ID: 23918157
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
