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 *

131 related articles for article (PubMed ID: 34335733)

  • 1. Hearing Screening Combined with Target Gene Panel Testing Increased Etiological Diagnostic Yield in Deaf Children.
    Xie L; Qiu Y; Jin Y; Xu K; Bai X; Liu XZ; Wang XH; Chen S; Sun Y
    Neural Plast; 2021; 2021():6151973. PubMed ID: 34335733
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Role of Targeted Next Generation Sequencing in the Etiological Work-Up of Congenitally Deaf Children.
    Boudewyns A; van den Ende J; Sommen M; Wuyts W; Peeters N; Van de Heyning P; Van Camp G
    Otol Neurotol; 2018 Jul; 39(6):732-738. PubMed ID: 29889784
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next-generation sequencing.
    Xiao C; Liu S; Wang H; Ding Y; Chen Y; Liu H
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1634. PubMed ID: 33638616
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay.
    Abe S; Yamaguchi T; Usami S
    Genet Test; 2007; 11(3):333-40. PubMed ID: 17949297
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
    Yu X; Lin Y; Xu J; Che T; Li L; Yang T; Wu H
    Orphanet J Rare Dis; 2020 Jan; 15(1):29. PubMed ID: 31992338
    [TBL] [Abstract][Full Text] [Related]  

  • 7. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
    Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).
    Prasad S; Cucci RA; Green GE; Smith RJ
    Hum Mutat; 2000 Dec; 16(6):502-8. PubMed ID: 11102979
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic screening of a Chinese cohort of children with hearing loss using a next-generation sequencing panel.
    Ma J; Ma X; Lin K; Huang R; Bi X; Ming C; Li L; Li X; Li G; Zhao L; Yang T; Gao Y; Zhang T
    Hum Genomics; 2023 Jan; 17(1):1. PubMed ID: 36597107
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Comprehensive molecular analysis of 61 Egyptian families with hereditary nonsyndromic hearing loss.
    Budde BS; Aly MA; Mohamed MR; Breß A; Altmüller J; Motameny S; Kawalia A; Thiele H; Konrad K; Becker C; Toliat MR; Nürnberg G; Sayed EAF; Mohamed ES; Pfister M; Nürnberg P
    Clin Genet; 2020 Jul; 98(1):32-42. PubMed ID: 32279305
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Prenatal genetic test and clinical guidance for 213 hereditary deaf families].
    Han MY; Lu YP; Bian XM; Wang LX; Huang SS; Wang GJ; Wang Y; Kang DY; Zhang X; Dai P
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Feb; 47(2):127-31. PubMed ID: 22455811
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [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]  

  • 13. GJB2 sequencing in deaf and profound sensorineural hearing loss children.
    Mielczarek M; Zakrzewska A; Olszewski J
    Otolaryngol Pol; 2016 Jun; 70(3):21-5. PubMed ID: 27386929
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Diagnostic methods and clinic application for mtDNA A1555G and GJB2 and SLC26A4 genes in deaf patients].
    Dai P; Yu F; Kang DY; Zhang X; Liu X; Mi WZ; Cao JY; Yuan HJ; Yang WY; Wu BL; Han DY
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2005 Oct; 40(10):769-73. PubMed ID: 16408730
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing.
    Bai X; Nian S; Feng L; Ruan Q; Luo X; Wu M; Yan Z
    Mol Genet Genomic Med; 2019 Aug; 7(8):e808. PubMed ID: 31250571
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mutation screening in non-syndromic hearing loss patients with cochlear implantation by massive parallel sequencing in Taiwan.
    Liu WH; Chang PY; Chang SC; Lu JJ; Wu CM
    PLoS One; 2019; 14(1):e0211261. PubMed ID: 30682115
    [TBL] [Abstract][Full Text] [Related]  

  • 17. DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System.
    Sommen M; Schrauwen I; Vandeweyer G; Boeckx N; Corneveaux JJ; van den Ende J; Boudewyns A; De Leenheer E; Janssens S; Claes K; Verstreken M; Strenzke N; Predöhl F; Wuyts W; Mortier G; Bitner-Glindzicz M; Moser T; Coucke P; Huentelman MJ; Van Camp G
    Hum Mutat; 2016 Aug; 37(8):812-9. PubMed ID: 27068579
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Revisiting Genetic Epidemiology with a Refined Targeted Gene Panel for Hereditary Hearing Impairment in the Taiwanese Population.
    Lee YH; Tsai CY; Lu YS; Lin PH; Chiang YT; Yang TH; Hsu JS; Hsu CJ; Chen PL; Liu TC; Wu CC
    Genes (Basel); 2023 Apr; 14(4):. PubMed ID: 37107638
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort.
    Bademci G; Foster J; Mahdieh N; Bonyadi M; Duman D; Cengiz FB; Menendez I; Diaz-Horta O; Shirkavand A; Zeinali S; Subasioglu A; Tokgoz-Yilmaz S; Huesca-Hernandez F; de la Luz Arenas-Sordo M; Dominguez-Aburto J; Hernandez-Zamora E; Montenegro P; Paredes R; Moreta G; Vinueza R; Villegas F; Mendoza-Benitez S; Guo S; Bozan N; Tos T; Incesulu A; Sennaroglu G; Blanton SH; Ozturkmen-Akay H; Yildirim-Baylan M; Tekin M
    Genet Med; 2016 Apr; 18(4):364-71. PubMed ID: 26226137
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of a cohort of children with sensory hearing loss using the SCALE systematic nomenclature.
    Sculerati N
    Laryngoscope; 2000 May; 110(5 Pt 1):787-98. PubMed ID: 10807358
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.