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.
98 related articles for article (PubMed ID: 26004784)
61. [Mutational analysis of 117 patients with non-syndromic hearing loss]. Wang L; Gu Y; Yang S; Mao H; Tang X; Xu T; Wu M; Sun Y; Luo X Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Feb; 36(2):108-111. PubMed ID: 30703224 [TBL] [Abstract][Full Text] [Related]
62. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574 [TBL] [Abstract][Full Text] [Related]
63. [Prenatal diagnosis for hereditary deaf families assisted by genetic testing]. Han B; Dai P; Qi QW; Wang LX; Wang Y; Bian XM; Wang QJ; Zhang X; Kang DY; Wang GJ; Han DY Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Sep; 42(9):660-3. PubMed ID: 18051563 [TBL] [Abstract][Full Text] [Related]
65. Deafness genes for nonsyndromic hearing loss and current studies in China. Xiao Z; Xie D Chin Med J (Engl); 2002 Jul; 115(7):1078-81. PubMed ID: 12173596 [TBL] [Abstract][Full Text] [Related]
66. [Genetic analysis and prenatal diagnosis for non-syndromic hearing impairment]. Wang L; Zhao HR; Liao S; Yang YL; Li T; Zhang B; Ding XB; Ma S; Liu HJ Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Oct; 30(5):518-21. PubMed ID: 24078562 [TBL] [Abstract][Full Text] [Related]
67. A quantitative cSMART assay for noninvasive prenatal screening of autosomal recessive nonsyndromic hearing loss caused by GJB2 and SLC26A4 mutations. Han M; Li Z; Wang W; Huang S; Lu Y; Gao Z; Wang L; Kang D; Li L; Liu Y; Xu M; Cram DS; Dai P Genet Med; 2017 Dec; 19(12):1309-1316. PubMed ID: 28541280 [TBL] [Abstract][Full Text] [Related]
68. [SLC26A4 mutations in a Chinese deafness family discovered by next-generation sequencing technology]. Mao J; Wei XM; Li H; Wang SN; Chen Y Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Nov; 47(11):942-5. PubMed ID: 23302201 [TBL] [Abstract][Full Text] [Related]
69. 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]
70. Novel Mutations in the TMPRSS3 Gene may Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss. Wong SH; Yen YC; Li SY; Yang JJ Int J Mol Sci; 2020 Mar; 21(7):. PubMed ID: 32235586 [TBL] [Abstract][Full Text] [Related]
71. MT-RNR1 Genotype Should Not Affect Childhood Vaccination-Unintended Consequences of Guidelines. McDermott JH; Wolf J; Newman WG JAMA Pediatr; 2023 Nov; 177(11):1119-1120. PubMed ID: 37695579 [TBL] [Abstract][Full Text] [Related]
72. Polygenic Risk Score for Early Prediction of Sepsis Risk in the Polytrauma Screening Cohort. Lu H; Wen D; Sun J; Du J; Qiao L; Zhang H; Zeng L; Zhang L; Jiang J; Zhang A Front Genet; 2020; 11():545564. PubMed ID: 33281864 [TBL] [Abstract][Full Text] [Related]
73. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden. Adadey SM; Wonkam-Tingang E; Twumasi Aboagye E; Nayo-Gyan DW; Boatemaa Ansong M; Quaye O; Awandare GA; Wonkam A Life (Basel); 2020 Oct; 10(11):. PubMed ID: 33126609 [TBL] [Abstract][Full Text] [Related]
74. Association of Polymorphisms in Candidate Genes with the Litter Size in Two Sheep Breeds. Yuan Z; Zhang J; Li W; Wang W; Li F; Yue X Animals (Basel); 2019 Nov; 9(11):. PubMed ID: 31726757 [TBL] [Abstract][Full Text] [Related]
75. Identification of Pathogenic Genes of Nonsyndromic Hearing Loss in Uyghur Families Using Massively Parallel DNA Sequencing Technique. Chen Y; Lu Y; Kuyaxi P; Cheng J; Zhao J; Zhao Q; Musha P; Zhang H; Yuan H Dis Markers; 2018; 2018():5298057. PubMed ID: 29692870 [TBL] [Abstract][Full Text] [Related]
76. SNPscan as a high-performance screening tool for mutation hotspots of hearing loss-associated genes. Li H; Wang B; Liu D; Wang T; Li Q; Wang W; Li H Genomics; 2015 Aug; 106(2):83-7. PubMed ID: 26004784 [TBL] [Abstract][Full Text] [Related]
77. Efficiency of microarray and SNPscan for the detection of hearing loss gene in 71 cases with nonsyndromic hearing loss. Han R; Li L; Duan L; Xia Y; Kuyaxi P; Zhao J; Zhao Q; Zhang H; Chen Y Medicine (Baltimore); 2017 Jun; 96(25):e7149. PubMed ID: 28640090 [TBL] [Abstract][Full Text] [Related]
78. [A novel technique for simultaneous multi-gene mutation screening in 225 patients with nonsyndromic hearing loss]. Zhang D; Duan H; Lin P; Cheng J; Wang C; Ma Y; Cheng Y; Zhao H; Wang W; Xu K; Han D; Yuan H Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Mar; 51(3):203-8. PubMed ID: 27033575 [TBL] [Abstract][Full Text] [Related]
79. A rapid method for simultaneous multi-gene mutation screening in children with nonsyndromic hearing loss. Du W; Cheng J; Ding H; Jiang Z; Guo Y; Yuan H Genomics; 2014 Oct; 104(4):264-70. PubMed ID: 25149764 [TBL] [Abstract][Full Text] [Related]
80. Clinical application of genetic testing for deafness. Smith RJ Am J Med Genet A; 2004 Sep; 130A(1):8-12. PubMed ID: 15368487 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]