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 *

158 related articles for article (PubMed ID: 22510577)

  • 41. 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]  

  • 42. Concurrent Genetic and Standard Screening for Hearing Impairment in 9317 Southern Chinese Newborns.
    Peng Q; Huang S; Liang Y; Ma K; Li S; Yang L; Li W; Ma Q; Liu Q; Zhong B; Lu X
    Genet Test Mol Biomarkers; 2016 Oct; 20(10):603-608. PubMed ID: 27541434
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Multi-Center in-Depth Screening of Neonatal Deafness Genes: Zhejiang, China.
    Cai L; Liu Y; Xu Y; Yang H; Lv L; Li Y; Chen Q; Lin X; Yang Y; Hu G; Zheng G; Zhou J; Qian Q; Xu MA; Fang J; Ding J; Chen W; Gao J
    Front Genet; 2021; 12():637096. PubMed ID: 34276761
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
    Norris VW; Arnos KS; Hanks WD; Xia X; Nance WE; Pandya A
    Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
    [TBL] [Abstract][Full Text] [Related]  

  • 45. [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]  

  • 46. Pregestational screening of hereditary deafness genes carriers in 10,684 normal pregnant women in Zhuzhou, China.
    Qi M; Lai H; Xu L; Zeng F; Zhang J; Xie K
    Birth Defects Res; 2021 May; 113(8):605-612. PubMed ID: 33470562
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Progressive hearing impairment with deletion in GJB2 gene despite normal newborn hearing screening].
    Prera N; Löhle E; Birkenhäger R
    Laryngorhinootologie; 2014 Apr; 93(4):244-8. PubMed ID: 24022696
    [TBL] [Abstract][Full Text] [Related]  

  • 48. The Frequency of Common Deafness-Associated Variants Among 3,555,336 Newborns in China and 141,456 Individuals Across Seven Populations Worldwide.
    Zhang J; Wang H; Yan C; Guan J; Yin L; Lan L; Li J; Zhao L; Wang Q
    Ear Hear; 2023 Jan-Feb 01; 44(1):232-241. PubMed ID: 36149380
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Prospective mutation screening of three common deafness genes in a large Taiwanese Cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities.
    Wu CC; Chen PJ; Chiu YH; Lu YC; Wu MC; Hsu CJ
    Audiol Neurootol; 2008; 13(3):172-81. PubMed ID: 18075246
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [Evaluation of deaf-mute patients with sensitive deafness gene screening in Shandong province].
    Ji YB; Han DY; Wang DY; Zhou Y; Zhao C; Wang H; Lan L; Wang QJ
    Zhonghua Yi Xue Za Zhi; 2009 Sep; 89(36):2531-5. PubMed ID: 20137612
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Hearing assessment and follow-up study of aeonatal deafness gene screening homozygous mutation infants].
    Liu QM; Tian Y; Yu JJ; He QQ; Peng L; Guo XQ; Li DY; Chen T; Wang F
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2019 Nov; 33(11):1089-1092. PubMed ID: 31914302
    [No Abstract]   [Full Text] [Related]  

  • 52. [Analysis of prenatal phenotype and pathogenetic variant in a fetus with Papillorenal syndrome].
    Zhao X; Yang D; Jia Y; Shou Y; Wang L; Wang X; Fu J; Guo H; Zhao J; Yin H; Zhang X; Zhu X; Gao L; Ma C; Xie Z; Shi M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Sep; 37(9):958-961. PubMed ID: 32820507
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [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]  

  • 54. [A new method for simultaneous multi-gene mutation screening in 355 patients with nonsyndromic hearing loss of Inner Mongolia Autonomous region].
    Zhang D; Duan H; Yuan H; Han D
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2015 Nov; 29(22):1941-6. PubMed ID: 26911054
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Early detection of neonatal hearing loss by otoacoustic emissions and auditory brainstem response over 10 years of experience.
    Escobar-Ipuz FA; Soria-Bretones C; García-Jiménez MA; Cueto EM; Torres Aranda AM; Sotos JM
    Int J Pediatr Otorhinolaryngol; 2019 Dec; 127():109647. PubMed ID: 31470205
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Incidence of the 35delG/GJB2 mutation in low-risk newborns.
    Zaputovic S; Stanojevic M; Medica I; Peterlin B; Petrovic O
    J Matern Fetal Neonatal Med; 2008 Jul; 21(7):463-8. PubMed ID: 18570126
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Analysis of deafness susceptibility gene of neonates in northern Guangdong, China.
    Ma Z; Huang W; Xu J; Qiu J; Liu Y; Ye M; Fan S
    Sci Rep; 2024 Jan; 14(1):362. PubMed ID: 38172182
    [TBL] [Abstract][Full Text] [Related]  

  • 58. GJB2 and mitochondrial 12S rRNA susceptibility mutations in sudden deafness.
    Chen K; Sun L; Zong L; Wu X; Zhan Y; Dong C; Cao H; Tang H; Jiang H
    Eur Arch Otorhinolaryngol; 2016 Jun; 273(6):1393-8. PubMed ID: 26119842
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Application of deafness diagnostic screening panel based on deafness mutation/gene database using invader assay.
    Abe S; Yamaguchi T; Usami S
    Genet Test; 2007; 11(3):333-40. PubMed ID: 17949297
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Neonatal detection of the 35delG mutation of the GJB2 gene in families at risk for deafness.
    Bathelier C; François M; Lucotte G
    Genet Couns; 2004; 15(1):61-6. PubMed ID: 15083701
    [TBL] [Abstract][Full Text] [Related]  

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