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 *

133 related articles for article (PubMed ID: 20437760)

  • 61. Genetic mutations in non-syndromic deafness patients in Hainan Province have a different mutational spectrum compared to patients from Mainland China.
    Huang B; Han M; Wang G; Huang S; Zeng J; Yuan Y; Dai P
    Int J Pediatr Otorhinolaryngol; 2018 May; 108():49-54. PubMed ID: 29605365
    [TBL] [Abstract][Full Text] [Related]  

  • 62. 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]  

  • 63. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
    Muskett JA; Chattaraj P; Heneghan JF; Reimold FR; Shmukler BE; Brewer CC; King KA; Zalewski CK; Shawker TH; Butman JA; Kenna MA; Chien WW; Alper SL; Griffith AJ
    Laryngoscope; 2016 Jul; 126(7):E240-7. PubMed ID: 26485571
    [TBL] [Abstract][Full Text] [Related]  

  • 64. SIX1 mutation associated with enlargement of the vestibular aqueduct in a patient with branchio-oto syndrome.
    Ito T; Noguchi Y; Yashima T; Kitamura K
    Laryngoscope; 2006 May; 116(5):796-9. PubMed ID: 16652090
    [TBL] [Abstract][Full Text] [Related]  

  • 65. Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan.
    Morisada N; Nozu K; Iijima K
    Pediatr Int; 2014 Jun; 56(3):309-14. PubMed ID: 24730701
    [TBL] [Abstract][Full Text] [Related]  

  • 66. 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]  

  • 67. A novel mutation in the SLC26A4 gene in a Chinese family with non-syndromic hearing loss and enlarged vestibular aqueduct.
    Liang Y; Peng Q; Wang K; Zhu P; Wu C; Rao C; Chang J; Li S; Lu X
    Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():97-100. PubMed ID: 29501320
    [TBL] [Abstract][Full Text] [Related]  

  • 68. Pathogenic substitution of IVS15 + 5G > A in SLC26A4 in patients of Okinawa Islands with enlarged vestibular aqueduct syndrome or Pendred syndrome.
    Ganaha A; Kaname T; Yanagi K; Naritomi K; Tono T; Usami S; Suzuki M
    BMC Med Genet; 2013 May; 14():56. PubMed ID: 23705809
    [TBL] [Abstract][Full Text] [Related]  

  • 69. [An analysis of the mutation in GJB2,GJB3,SLC26A4 and mtDNA12SrRNA in new born].
    Chai F; Zhao HL; Qiu SQ
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2017 May; 31(9):664-666. PubMed ID: 29871341
    [No Abstract]   [Full Text] [Related]  

  • 70. [Prenatal genetic counseling and instruction for deaf families by genetic test].
    Han MY; Huang SS; Wang GJ; Yuan YY; Kang DY; Zhang X; Dai P
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2011 Nov; 46(11):909-13. PubMed ID: 22335977
    [TBL] [Abstract][Full Text] [Related]  

  • 71. Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review.
    Tsukada K; Nishio SY; Hattori M; Usami S
    Ann Otol Rhinol Laryngol; 2015 May; 124 Suppl 1():61S-76S. PubMed ID: 25999548
    [TBL] [Abstract][Full Text] [Related]  

  • 72. Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China.
    Chai Y; Huang Z; Tao Z; Li X; Li L; Li Y; Wu H; Yang T
    Am J Med Genet A; 2013 Sep; 161A(9):2226-33. PubMed ID: 23918157
    [TBL] [Abstract][Full Text] [Related]  

  • 73. [Study of newborn hearing and genetic screening in Jinan].
    Xiang L; Lin Q; Nie W; Hou Q; Li H; Li Y; Liu X
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 May; 50(5):401-5. PubMed ID: 26178053
    [TBL] [Abstract][Full Text] [Related]  

  • 74. Genetic architecture and phenotypic landscape of SLC26A4-related hearing loss.
    Honda K; Griffith AJ
    Hum Genet; 2022 Apr; 141(3-4):455-464. PubMed ID: 34345941
    [TBL] [Abstract][Full Text] [Related]  

  • 75. Intrafamilial phenotypic variability in families with biallelic SLC26A4 mutations.
    Song MH; Shin JW; Park HJ; Lee KA; Kim Y; Kim UK; Jeon JH; Choi JY
    Laryngoscope; 2014 May; 124(5):E194-202. PubMed ID: 24338212
    [TBL] [Abstract][Full Text] [Related]  

  • 76. Genetics of Hearing Loss--Nonsyndromic.
    Chang KW
    Otolaryngol Clin North Am; 2015 Dec; 48(6):1063-72. PubMed ID: 26275501
    [TBL] [Abstract][Full Text] [Related]  

  • 77. [Molecular etiology analysis among students with profound hearing loss in a special education school in Yangzhou].
    Peng X; Li X; Xu L; Guan B; Zhang J; Yu A
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Jul; 26(13):577-80. PubMed ID: 23002639
    [TBL] [Abstract][Full Text] [Related]  

  • 78. Mutation Spectrum of Common Deafness-Causing Genes in Patients with Non-Syndromic Deafness in the Xiamen Area, China.
    Jiang Y; Huang S; Deng T; Wu L; Chen J; Kang D; Xu X; Li R; Han D; Dai P
    PLoS One; 2015; 10(8):e0135088. PubMed ID: 26252218
    [TBL] [Abstract][Full Text] [Related]  

  • 79. Compound heterozygous mutations of SLC26A4 in 4 Chinese families with enlarged vestibular aqueduct.
    Yao G; Li S; Chen D; Wang H; Zhang J; Feng Z; Guo L; Yang Z; Yang S; Sun C; Zhang X; Ma D
    Int J Pediatr Otorhinolaryngol; 2013 Apr; 77(4):544-9. PubMed ID: 23385134
    [TBL] [Abstract][Full Text] [Related]  

  • 80. Suspension array-based deafness genetic screening in 53,033 Chinese newborns identifies high prevalence of 109 G>A in GJB2.
    Zou Y; Dai QQ; Tao WJ; Wen XL; Feng DF; Deng H; Zhou WP; Li M; Zhang L
    Int J Pediatr Otorhinolaryngol; 2019 Nov; 126():109630. PubMed ID: 31442870
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.