BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

193 related articles for article (PubMed ID: 34304520)

  • 1. [Advances in studies on genetics of syndromes combining sensorineural hearing loss with scoliosis].
    Wu K; Li Z; Zhang Q
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Jun; 35(6):556-562. PubMed ID: 34304520
    [No Abstract]   [Full Text] [Related]  

  • 2. [Hereditary hearing loss].
    Tropitzsch A; Schade-Mann T; Gamerdinger P
    HNO; 2023 Feb; 71(2):131-142. PubMed ID: 36526931
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [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]  

  • 4. [Phenotype and genotype analysis of recessive hereditary moderate sensorineural hearing loss caused by new mutations in OTOGL gene].
    Feng ML; Huang SS; Tang FZ; Zhang X; Li XH; Qiu SW; Yuan YY
    Zhonghua Yi Xue Za Zhi; 2021 Jan; 101(2):115-121. PubMed ID: 33455126
    [No Abstract]   [Full Text] [Related]  

  • 5. Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies.
    Masindova I; Varga L; Stanik J; Valentinova L; Profant M; Klimes I; Gasperikova D
    Endocr Regul; 2012 Jul; 46(3):167-86. PubMed ID: 22808909
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A case report of congenital sensorineural deafness caused by novel mutation in Usher1C and related literature analysis].
    Guo M; Han W; Li S
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2020 Jun; 34(6):562-564. PubMed ID: 32842192
    [No Abstract]   [Full Text] [Related]  

  • 7. Genetics of non-syndromic hearing loss in the Middle East.
    Najmabadi H; Kahrizi K
    Int J Pediatr Otorhinolaryngol; 2014 Dec; 78(12):2026-36. PubMed ID: 25281338
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Clinical heterogeneity of the SLC26A4 gene in UAE patients with hearing loss and bioinformatics investigation of DFNB4/Pendred syndrome missense mutations.
    Chouchen J; Mahfood M; Alobathani M; Eldin Mohamed WK; Tlili A
    Int J Pediatr Otorhinolaryngol; 2021 Jan; 140():110467. PubMed ID: 33199029
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
    Mutai H; Suzuki N; Shimizu A; Torii C; Namba K; Morimoto N; Kudoh J; Kaga K; Kosaki K; Matsunaga T
    Orphanet J Rare Dis; 2013 Oct; 8():172. PubMed ID: 24164807
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Non-syndromic dominant sensorineural hearing loss: from a few phenotypes to many genotypes.
    Stinckens C; Ensink R; Feenstra L; Fryns JP; Cremers C
    Int J Pediatr Otorhinolaryngol; 1997 Jan; 38(3):237-45. PubMed ID: 9051428
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [A review of diagnosis and treatment of syndromic hearing loss].
    Liu M; Zhang T
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2021 Mar; 35(3):285-288. PubMed ID: 33794621
    [No Abstract]   [Full Text] [Related]  

  • 12. [Non-syndromic hereditary hearing impairment].
    Birkenhäger R; Aschendorff A; Schipper J; Laszig R
    Laryngorhinootologie; 2007 Apr; 86(4):299-309; quiz 310-3. PubMed ID: 17407011
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.
    Schrijver I
    J Mol Diagn; 2004 Nov; 6(4):275-84. PubMed ID: 15507665
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Investigation of clinical features and detection of 79 known deafness genes in a large Chinese family with dominant non-syndromic hearing loss].
    Lin X; Chen D; Wu H; Yang T; Zhang D; Chai Y
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2014 Aug; 49(8):654-8. PubMed ID: 25351123
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Research progress on hereditary endocrine and metabolic diseases associated with sensorineural hearing loss].
    Chen F; Zhang Q; Zhang Q; Wang Q
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2024 Jan; 38(1):63-69. PubMed ID: 38297851
    [No Abstract]   [Full Text] [Related]  

  • 16. Genetic investigations in childhood deafness.
    Parker M; Bitner-Glindzicz M
    Arch Dis Child; 2015 Mar; 100(3):271-8. PubMed ID: 25324569
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Deafness genes.
    Kitamura K; Takahashi K; Tamagawa Y; Noguchi Y; Kuroishikawa Y; Ishikawa K; Hagiwara H
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Value of genetic testing in the otological approach for sensorineural hearing loss.
    Matsunaga T
    Keio J Med; 2009 Dec; 58(4):216-22. PubMed ID: 20037285
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [Genetics of congenital deafness].
    Faundes V; Pardo RA; Castillo Taucher S
    Med Clin (Barc); 2012 Oct; 139(10):446-51. PubMed ID: 22538062
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.