These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

291 related articles for article (PubMed ID: 30970410)

  • 1. [The analysis of mutations in non-syndromic deafness gene SLC26A4 by next generation sequencing technology].
    Chai F; Zhao HL; Han XD
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Apr; 33(4):357-361. PubMed ID: 30970410
    [No Abstract]   [Full Text] [Related]  

  • 2. [Application of next generation sequencing in congenital sensorineural deafness].
    Xu B; Chen Y; Jiang A; Chen C; Wang K; Zheng J; Fu Y
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):811-815. PubMed ID: 29921047
    [No Abstract]   [Full Text] [Related]  

  • 3. [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]  

  • 4. [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]  

  • 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. 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]  

  • 7. The correlation between deafness progression and SLC26A4 mutations in enlarged vestibular aqueduct patients.
    Yu K; Liu X; Yang B
    Eur Arch Otorhinolaryngol; 2024 Feb; 281(2):649-654. PubMed ID: 37477685
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 9. 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]  

  • 10. 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]  

  • 11. The mutation frequencies of GJB2, GJB3, SLC26A4 and MT-RNR1 of patients with severe to profound sensorineural hearing loss in northwest China.
    Liu XW; Wang JC; Wang SY; Li SJ; Zhu YM; Ding WJ; Xu CY; Duan L; Xu BC; Guo YF
    Int J Pediatr Otorhinolaryngol; 2020 Sep; 136():110143. PubMed ID: 32645618
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. 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]  

  • 15. 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]  

  • 16. [Difference of
    Liu Y; Huang Z; Sun C; Shen X; Li W; Li Q
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Oct; 35(10):891-895. PubMed ID: 34628810
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. [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]  

  • 19. [Analysis of genotypes and audiological characteristics of children with SLC26A4 gene pathogenic mutations].
    Zhao XL; Huang LH; Wang XY; DU Y; Wang X; Cheng XH; Zhao LP; Li Y
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2018 Jun; 32(11):836-840. PubMed ID: 29921053
    [No Abstract]   [Full Text] [Related]  

  • 20. Identification of SLC26A4 mutations p.L582LfsX4, p.I188T and p.E704K in a Chinese family with large vestibular aqueduct syndrome (LVAS).
    Li Y; Zhu B; Su J; Yin Y; Yu F
    Int J Pediatr Otorhinolaryngol; 2016 Dec; 91():1-5. PubMed ID: 27863619
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 15.