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 *

149 related articles for article (PubMed ID: 15368487)

  • 61. [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]  

  • 62. On the origin and frequency of the 35delG allele in GJB2-linked deafness in Europe.
    Anichkina A; Kulenich T; Zinchenko S; Shagina I; Polyakov A; Ginter E; Evgrafov O; Viktorova T; Khusnitdonova E
    Eur J Hum Genet; 2001 Feb; 9(2):151. PubMed ID: 11313751
    [No Abstract]   [Full Text] [Related]  

  • 63. Targeted Linked-Read Sequencing for Direct Haplotype Phasing of Parental GJB2/SLC26A4 Alleles: A Universal and Dependable Noninvasive Prenatal Diagnosis Method Applied to Autosomal Recessive Nonsyndromic Hearing Loss in At-Risk Families.
    Gao B; Jiang Y; Han M; Ji X; Zhang D; Wu L; Gao X; Huang S; Zhao C; Su Y; Yang S; Zhang X; Liu N; Han L; Wang L; Ren L; Yang J; Wu J; Yuan Y; Dai P
    J Mol Diagn; 2024 Jul; 26(7):638-651. PubMed ID: 38663495
    [TBL] [Abstract][Full Text] [Related]  

  • 64. Different cortical metabolic activation by visual stimuli possibly due to different time courses of hearing loss in patients with GJB2 and SLC26A4 mutations.
    Moteki H; Naito Y; Fujiwara K; Kitoh R; Nishio SY; Oguchi K; Takumi Y; Usami S
    Acta Otolaryngol; 2011 Nov; 131(11):1232-6. PubMed ID: 21728752
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Mutation spectrum and hotspots of the common deafness genes in 314 patients with nonsyndromic hearing loss in Heze area, China.
    Zhang M; Han Y; Zhang F; Bai X; Wang H
    Acta Otolaryngol; 2019 Jul; 139(7):612-617. PubMed ID: 31107121
    [No Abstract]   [Full Text] [Related]  

  • 66. Long term speech perception after cochlear implant in pediatric patients with GJB2 mutations.
    Yoshida H; Takahashi H; Kanda Y; Usami S
    Auris Nasus Larynx; 2013 Oct; 40(5):435-9. PubMed ID: 23477838
    [TBL] [Abstract][Full Text] [Related]  

  • 67. Deafness and mutations in the connexin 26 gene.
    Zlotogora J
    N Engl J Med; 1999 Apr; 340(16):1288. PubMed ID: 10215495
    [No Abstract]   [Full Text] [Related]  

  • 68. Deafness genes and their diagnostic applications.
    Cryns K; Van Camp G
    Audiol Neurootol; 2004; 9(1):2-22. PubMed ID: 14676470
    [TBL] [Abstract][Full Text] [Related]  

  • 69. Mutations in the connexin 26 gene (GJB2) among Ashkenazi Jews with nonsyndromic recessive deafness.
    Morell RJ; Kim HJ; Hood LJ; Goforth L; Friderici K; Fisher R; Van Camp G; Berlin CI; Oddoux C; Ostrer H; Keats B; Friedman TB
    N Engl J Med; 1998 Nov; 339(21):1500-5. PubMed ID: 9819448
    [TBL] [Abstract][Full Text] [Related]  

  • 70. Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment.
    Wu CC; Lu YC; Chen PJ; Liu AY; Hwu WL; Hsu CJ
    Laryngoscope; 2009 Dec; 119(12):2411-6. PubMed ID: 19718752
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Hereditary deafness and phenotyping in humans.
    Bitner-Glindzicz M
    Br Med Bull; 2002; 63():73-94. PubMed ID: 12324385
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
    Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L
    Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641
    [TBL] [Abstract][Full Text] [Related]  

  • 73. High-throughput screening for GJB2 mutations--its clinical application to genetic testing in prelingual deafness screening for GJB2 mutations.
    Sugata A; Fukushima K; Sugata K; Fukuda S; Kimura N; Gunduz M; Kasai N; Usami S; Smith RJ; Nishizaki K
    Auris Nasus Larynx; 2002 Jul; 29(3):231-9. PubMed ID: 12167443
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Etiology of unilateral hearing loss in a national hereditary deafness repository.
    Dodson KM; Georgolios A; Barr N; Nguyen B; Sismanis A; Arnos KS; Norris VW; Chapman D; Nance WE; Pandya A
    Am J Otolaryngol; 2012; 33(5):590-4. PubMed ID: 22534022
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family.
    Kelsell DP; Wilgoss AL; Richard G; Stevens HP; Munro CS; Leigh IM
    Eur J Hum Genet; 2000 Feb; 8(2):141-4. PubMed ID: 10757647
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Genetic screening for deafness.
    Smith RJ; Hone S
    Pediatr Clin North Am; 2003 Apr; 50(2):315-29. PubMed ID: 12809325
    [TBL] [Abstract][Full Text] [Related]  

  • 77. Mutation Analysis of the Common Deafness Genes in Patients with Nonsyndromic Hearing Loss in Linyi by SNPscan Assay.
    Zhang F; Xiao Y; Xu L; Zhang X; Zhang G; Li J; Lv H; Bai X; Wang H
    Biomed Res Int; 2016; 2016():1302914. PubMed ID: 27247933
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Genetic Epidemiology and Clinical Features of Hereditary Hearing Impairment in the Taiwanese Population.
    Wu CC; Tsai CY; Lin YH; Chen PY; Lin PH; Cheng YF; Wu CM; Lin YH; Lee CY; Erdenechuluun J; Liu TC; Chen PL; Hsu CJ
    Genes (Basel); 2019 Oct; 10(10):. PubMed ID: 31581539
    [TBL] [Abstract][Full Text] [Related]  

  • 79. [Analysis of deafness gene variant screening of 7875 neonatal cases in Dongying area of Shandong].
    Tian M; Cao Y; Chen Z; Qi L; Liu A; Li H; Bo Q; Liu Q
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):962-967. PubMed ID: 32820508
    [TBL] [Abstract][Full Text] [Related]  

  • 80. A fully integrated SNP genotyping system for hereditary hearing-loss detection.
    Li N; Zhang Y; Shen M; Xu Y
    Lab Chip; 2022 Feb; 22(4):697-708. PubMed ID: 34923580
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.