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 *

114 related articles for article (PubMed ID: 19266817)

  • 41. The H723R mutation in the PDS/SLC26A4 gene is associated with typical Pendred syndrome in Korean patients.
    Cho MA; Jeong SJ; Eom SM; Park HY; Lee YJ; Park SE; Park SY; Rhee Y; Kang ES; Ahn CW; Cha BS; Lee EJ; Kim KR; Lee HC; Lim SK
    Endocrine; 2006 Oct; 30(2):237-43. PubMed ID: 17322586
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Genotyping and audiological characteristics of infants with a single-allele SLC26A4 mutation.
    Zhao X; Huang L; Wang X; Wang X; Zhao L; Cheng X; Ruan Y
    Int J Pediatr Otorhinolaryngol; 2019 Jan; 116():153-158. PubMed ID: 30554688
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or Pendred syndrome.
    Wu CC; Lu YC; Chen PJ; Yeh PL; Su YN; Hwu WL; Hsu CJ
    Audiol Neurootol; 2010; 15(1):57-66. PubMed ID: 19648736
    [TBL] [Abstract][Full Text] [Related]  

  • 44. [Frequency of SLC26A4 IVS7-2A > G mutation in patients with severe to profound hearing loss from different area and ethnic group in China].
    Li Q; Dai P; Huang DL; Yuan YY; Zhu QW; Han B; Liu X; Yu F; Kang DY; Zhang X; Xue DD; Jin ZC
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Dec; 42(12):893-7. PubMed ID: 18335745
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Selection of Diagnostically Significant Regions of the
    Danilchenko VY; Zytsar MV; Maslova EA; Posukh OL
    Int J Mol Sci; 2022 Nov; 23(21):. PubMed ID: 36362242
    [TBL] [Abstract][Full Text] [Related]  

  • 46. A systematic review and meta-analysis of common mutations of SLC26A4 gene in Asian populations.
    Du W; Guo Y; Wang C; Wang Y; Liu X
    Int J Pediatr Otorhinolaryngol; 2013 Oct; 77(10):1670-6. PubMed ID: 23958391
    [TBL] [Abstract][Full Text] [Related]  

  • 47. [Molecular and functional testing in case of hereditary hearing loss associated with the SLC26A4 gene].
    Roesch S; Bernardinelli E; Wortmann S; Mayr JA; Bader I; Schweighofer-Zwink G; Rasp G; Dossena S
    Laryngorhinootologie; 2020 Dec; 99(12):853-862. PubMed ID: 33307573
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.
    Cengiz FB; Yilmazer R; Olgun L; Sennaroglu L; Kirazli T; Alper H; Olgun Y; Incesulu A; Atik T; Huesca-Hernandez F; Domínguez-Aburto J; González-Rosado G; Hernandez-Zamora E; Arenas-Sordo ML; Menendez I; Orhan KS; Avci H; Mahdieh N; Bonyadi M; Foster J; Duman D; Ozkinay F; Blanton SH; Bademci G; Tekin M
    Int J Pediatr Otorhinolaryngol; 2017 Oct; 101():167-171. PubMed ID: 28964290
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Port-wine stains associated with large vestibular aqueduct syndrome caused by mutations in GNAQ and SLC26A4 genes: A case report.
    Cong T; Liu L; Zhang H; Wang L; Jiang X
    J Dermatol; 2020 Jan; 47(1):78-81. PubMed ID: 31692010
    [TBL] [Abstract][Full Text] [Related]  

  • 50. [The molecular epidemiology analysis of heavy-profound hearing loss in Nangtong].
    Wang Q; You Y; Zhang Q
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2013 Apr; 27(7):366-70. PubMed ID: 23833990
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Novel splice-site mutation c.1615-2A>G (IVS14-2A>G) in the SLC26A4 gene causing Pendred syndrome in a consanguineous Portuguese family.
    Simões-Teixeira H; Matos TD; Marques MC; Dias O; Andrea M; Barreiros E; Barreiros L; Moreno F; Fialho G; Caria H; Del Castillo I
    Am J Med Genet A; 2011 Apr; 155A(4):924-7. PubMed ID: 21416585
    [No Abstract]   [Full Text] [Related]  

  • 52. Screening of SLC26A4 Gene Hotspots in 2673 Patients Associated with Sensorineural Hearing Loss in Northwestern China.
    Wang Y; Li Y; Xu B; Zhu Y; Chen X; Guo Y
    J Int Adv Otol; 2022 Mar; 18(2):92-95. PubMed ID: 35418354
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Novel CRISPR/Cas12a-based genetic diagnostic approach for SLC26A4 mutation-related hereditary hearing loss.
    Jin X; Zhang L; Wang X; An L; Huang S; Dai P; Gao H; Ma X
    Eur J Med Genet; 2022 Feb; 65(2):104406. PubMed ID: 34968750
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A Family of H723R Mutation for SLC26A4 Associated with Enlarged Vestibular Aqueduct Syndrome.
    Kim S; Song DG; Bae JW; Choi SY; Kim UK; Choi YJ; Lee KY; Lee SH; Lee JR
    Clin Exp Otorhinolaryngol; 2009 Jun; 2(2):100-2. PubMed ID: 19565036
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Heterogeneity of Hereditary Hearing Loss in Iran: a Comprehensive Review.
    Beheshtian M; Babanejad M; Azaiez H; Bazazzadegan N; Kolbe D; Sloan-Heggen C; Arzhangi S; Booth K; Mohseni M; Frees K; Azizi MH; Daneshi A; Farhadi M; Kahrizi K; Smith RJ; Najmabadi H
    Arch Iran Med; 2016 Oct; 19(10):720-728. PubMed ID: 27743438
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Complex Phenotypic Presentation of Syndromic Hearing Loss Deciphered as Three Separate Clinical Entities: How Genetic Testing Guides Final Diagnosis.
    Bałdyga N; Sarosiak A; Oziębło D; Furmanek M; Szulborski K; Szaflik JP; Skarżyński H; Ołdak M
    Audiol Neurootol; 2021; 26(4):226-235. PubMed ID: 33352548
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Etiologic diagnosis of sensorineural hearing loss in adults.
    Angeli SI; Yan D; Telischi F; Balkany TJ; Ouyang XM; Du LL; Eshraghi A; Goodwin L; Liu XZ
    Otolaryngol Head Neck Surg; 2005 Jun; 132(6):890-5. PubMed ID: 15944560
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey.
    Tekin M; Akçayöz D; Comak E; Boğoçlu G; Duman T; Fitoz S; Ilhan I; Akar N
    Clin Genet; 2003 Oct; 64(4):371-4. PubMed ID: 12974744
    [No Abstract]   [Full Text] [Related]  

  • 59. [Genotypic analysis of familial dilated vestibular aqueduct syndrome].
    Dai P; Han D; Cao J; Zhai S; Kang D; Liu X; Yuan H; Zhang X; Li M; Liu L; Feng B; Yang W; Wu B
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2006 Feb; 20(4):147-50. PubMed ID: 16711435
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome.
    Tabatabaiefar MA; Alasti F; Peeters N; Wuyts W; Nooridaloii MR; Chaleshtori MH; Van Camp G
    Hum Genet; 2010 Apr; 127(4):468-9. PubMed ID: 21488234
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.