BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

112 related articles for article (PubMed ID: 25752129)

  • 1. [Next-generation sequencing in molecular diagnosis of hereditary hearing loss].
    Du W; Guo Y
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2014 Nov; 28(22):1815-8. PubMed ID: 25752129
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pediatric otolaryngology, molecular diagnosis of hereditary hearing loss: next-generation sequencing approach.
    Jasper KM; Jamshidi A; Reilly BK
    Curr Opin Otolaryngol Head Neck Surg; 2015 Dec; 23(6):480-4. PubMed ID: 26488533
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.
    Sivakumaran TA; Husami A; Kissell D; Zhang W; Keddache M; Black AP; Tinkle BT; Greinwald JH; Zhang K
    Otolaryngol Head Neck Surg; 2013 Jun; 148(6):1007-16. PubMed ID: 23525850
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. Next-generation sequencing facilitates genetic diagnosis and improves the management of patients with hearing loss in clinical practice.
    Liu C; Huang Y; Zhang Y; Ding H; Yu L; Wang A; Wang Y; Zeng Y; Liu L; Liu Y; Qi Y; Li F; Wu J; Du L; Mai F; Zhang Q; Wang X; Yin A
    Int J Pediatr Otorhinolaryngol; 2022 Oct; 161():111258. PubMed ID: 35939872
    [TBL] [Abstract][Full Text] [Related]  

  • 6. The Application of Next-Generation Sequencing for Mutation Detection in Autosomal-Dominant Hereditary Hearing Impairment.
    Gürtler N; Röthlisberger B; Ludin K; Schlegel C; Lalwani AK
    Otol Neurotol; 2017 Jul; 38(6):900-903. PubMed ID: 28419064
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Clinical utility of next-generation sequencing in the aetiological diagnosis of sensorineural hearing loss in a Childhood Hearing Loss Unit.
    Costales M; Diñeiro M; Cifuentes GA; Capín R; Otero A; Viejo-Díaz M; Plasencia A; Núñez F; Gómez JR; Llorente JL; Cadiñanos J; Cabanillas R
    Acta Otorrinolaringol Esp (Engl Ed); 2020; 71(3):166-174. PubMed ID: 31706454
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Next generation sequencing and genetics of hereditary hearing loss in the iranian population: New insights from a systematic review.
    Koohiyan M
    Int J Pediatr Otorhinolaryngol; 2020 Feb; 129():109756. PubMed ID: 31704577
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.
    Asgharzade S; Tabatabaiefar MA; Mohammadi-Asl J; Chaleshtori MH
    Int J Pediatr Otorhinolaryngol; 2018 May; 108():8-11. PubMed ID: 29605370
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Improving the Management of Patients with Hearing Loss by the Implementation of an NGS Panel in Clinical Practice.
    García-García G; Berzal-Serrano A; García-Díaz P; Villanova-Aparisi R; Juárez-Rodríguez S; de Paula-Vernetta C; Cavallé-Garrido L; Jaijo T; Armengot-Carceller M; Millán JM; Aller E
    Genes (Basel); 2020 Dec; 11(12):. PubMed ID: 33297549
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Application and progress of high-throughput sequencing technologies in the research of hereditary hearing loss.
    Wang CC; Yuan HJ
    Yi Chuan; 2017 Mar; 39(3):208-219. PubMed ID: 28420617
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetics of Hearing Loss: Syndromic.
    Koffler T; Ushakov K; Avraham KB
    Otolaryngol Clin North Am; 2015 Dec; 48(6):1041-61. PubMed ID: 26443487
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Molecular diagnostics for hereditary hearing loss in children.
    Sommen M; Wuyts W; Van Camp G
    Expert Rev Mol Diagn; 2017 Aug; 17(8):751-760. PubMed ID: 28593790
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Whole-exome sequencing and its impact in hereditary hearing loss.
    Atik T; Bademci G; Diaz-Horta O; Blanton SH; Tekin M
    Genet Res (Camb); 2015 Mar; 97():e4. PubMed ID: 25825321
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Establishment of a Flexible Real-Time Polymerase Chain Reaction-Based Platform for Detecting Prevalent Deafness Mutations Associated with Variable Degree of Sensorineural Hearing Loss in Koreans.
    Han KH; Kim AR; Kim MY; Ahn S; Oh SH; Song JH; Choi BY
    PLoS One; 2016; 11(9):e0161756. PubMed ID: 27583405
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetic studies in a patient with X-linked retinoschisis coexisting with developmental delay and sensorineural hearing loss.
    Sudha D; Patric IRP; Ganapathy A; Agarwal S; Krishna S; Neriyanuri S; Sripriya S; Sen P; Chidambaram S; Arunachalam JP
    Ophthalmic Genet; 2017; 38(3):260-266. PubMed ID: 28574807
    [TBL] [Abstract][Full Text] [Related]  

  • 18. A novel mutation of the EYA4 gene associated with post-lingual hearing loss in a proband is co-segregating with a novel PAX3 mutation in two congenitally deaf family members.
    Cesca F; Bettella E; Polli R; Cama E; Scimemi P; Santarelli R; Murgia A
    Int J Pediatr Otorhinolaryngol; 2018 Jan; 104():88-93. PubMed ID: 29287889
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Application of next generation sequencing in gene identification and genetic diagnosis of hereditary hearing loss].
    Huijun Y; Yu L
    Yi Chuan; 2014 Nov; 36(11):1112-20. PubMed ID: 25567869
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Emberger syndrome: A rare association with hearing loss.
    Zawawi F; Sokolov M; Mawby T; Gordon KA; Papsin BC; Cushing SL
    Int J Pediatr Otorhinolaryngol; 2018 May; 108():82-84. PubMed ID: 29605372
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.