BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

414 related articles for article (PubMed ID: 12162522)

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

  • 22. Hereditary non-syndromic sensorineural hearing loss: transforming silence to sound.
    Schrijver I
    J Mol Diagn; 2004 Nov; 6(4):275-84. PubMed ID: 15507665
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Molecular analysis of the heterogeneity of hereditary monosymptomatic sensorineural hearing loss].
    Fiegert P; Lamprecht-Dinnesen A; Preisler-Adams S; Deufel T
    Laryngorhinootologie; 1996 Mar; 75(3):141-7. PubMed ID: 8652029
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Novel missense mutations in MYO7A underlying postlingual high- or low-frequency non-syndromic hearing impairment in two large families from China.
    Sun Y; Chen J; Sun H; Cheng J; Li J; Lu Y; Lu Y; Jin Z; Zhu Y; Ouyang X; Yan D; Dai P; Han D; Yang W; Wang R; Liu X; Yuan H
    J Hum Genet; 2011 Jan; 56(1):64-70. PubMed ID: 21150918
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Molecular analysis of the TMPRSS3 gene in Moroccan families with non-syndromic hearing loss.
    Charif M; Abidi O; Boulouiz R; Nahili H; Rouba H; Kandil M; Delprat B; Lenaers G; Barakat A
    Biochem Biophys Res Commun; 2012 Mar; 419(4):643-7. PubMed ID: 22382023
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [A family with nonsyndromic hearing impairment caused by intermarry].
    Shu AL; Nie YZ
    Yi Chuan; 2005 Jul; 27(4):553-6. PubMed ID: 16120576
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Deletion of the entire POU4F3 gene in a familial case of autosomal dominant non-syndromic hearing loss.
    Freitas ÉL; Oiticica J; Silva AG; Bittar RS; Rosenberg C; Mingroni-Netto RC
    Eur J Med Genet; 2014 Mar; 57(4):125-8. PubMed ID: 24556497
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A novel missense mutation in ACTG1 causes dominant deafness in a Norwegian DFNA20/26 family, but ACTG1 mutations are not frequent among families with hereditary hearing impairment.
    Rendtorff ND; Zhu M; Fagerheim T; Antal TL; Jones M; Teslovich TM; Gillanders EM; Barmada M; Teig E; Trent JM; Friderici KH; Stephan DA; Tranebjaerg L
    Eur J Hum Genet; 2006 Oct; 14(10):1097-105. PubMed ID: 16773128
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Mapping of gene underlying autosomal dominant non-syndromic hearing loss(DFNA)].
    Sun HJ; Tao R; Cheng J; Yang SZ; Cao JY; Yu LM; Hong MD; Feng GY; Dai P; Yuan HJ; Han DY; He L
    Yi Chuan; 2006 Dec; 28(12):1489-94. PubMed ID: 17138532
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Mapping of a new autosomal dominant non-syndromic hearing loss locus (DFNA43) to chromosome 2p12.
    Flex E; Mangino M; Mazzoli M; Martini A; Migliosi V; Colosimo A; Mingarelli R; Pizzuti A; Dallapiccola B
    J Med Genet; 2003 Apr; 40(4):278-81. PubMed ID: 12676899
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Molecular and hereditary mechanisms of sensorineural hearing loss with focus on selected endocrinopathies.
    Masindova I; Varga L; Stanik J; Valentinova L; Profant M; Klimes I; Gasperikova D
    Endocr Regul; 2012 Jul; 46(3):167-86. PubMed ID: 22808909
    [TBL] [Abstract][Full Text] [Related]  

  • 32. A gene for a dominant form of non-syndromic sensorineural deafness (DFNA11) maps within the region containing the DFNB2 recessive deafness gene.
    Tamagawa Y; Kitamura K; Ishida T; Ishikawa K; Tanaka H; Tsuji S; Nishizawa M
    Hum Mol Genet; 1996 Jun; 5(6):849-52. PubMed ID: 8776602
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Pattern of connexin 26 (GJB2) mutations causing sensorineural hearing impairment in Ghana.
    Hamelmann C; Amedofu GK; Albrecht K; Muntau B; Gelhaus A; Brobby GW; Horstmann RD
    Hum Mutat; 2001; 18(1):84-5. PubMed ID: 11439000
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Non-syndromic, autosomal-recessive deafness.
    Petersen MB; Willems PJ
    Clin Genet; 2006 May; 69(5):371-92. PubMed ID: 16650073
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment.
    Qu R; Sang Q; Xu Y; Feng R; Jin L; He L; Wang L
    Int J Pediatr Otorhinolaryngol; 2016 May; 84():43-7. PubMed ID: 27063751
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Analysis of a cohort of children with sensory hearing loss using the SCALE systematic nomenclature.
    Sculerati N
    Laryngoscope; 2000 May; 110(5 Pt 1):787-98. PubMed ID: 10807358
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genetics of non-syndromic hearing loss in the Middle East.
    Najmabadi H; Kahrizi K
    Int J Pediatr Otorhinolaryngol; 2014 Dec; 78(12):2026-36. PubMed ID: 25281338
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Congenital cochlear deafness in mitochondrial diseases related to RRM2B and SERAC1 gene defects. A study of the mitochondrial patients of the CMHI hospital in Warsaw, Poland.
    Iwanicka-Pronicka K; Ciara E; Piekutowska-Abramczuk D; Halat P; Pajdowska M; Pronicki M
    Int J Pediatr Otorhinolaryngol; 2019 Jun; 121():143-149. PubMed ID: 30909120
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Genetic aspects of congenital sensorineural hearing loss].
    Blanchard M; Thierry B; Marlin S; Denoyelle F
    Arch Pediatr; 2012 Aug; 19(8):886-9. PubMed ID: 22770557
    [TBL] [Abstract][Full Text] [Related]  

  • 40. ATP6B1 gene mutations associated with distal renal tubular acidosis and deafness in a child.
    Hahn H; Kang HG; Ha IS; Cheong HI; Choi Y
    Am J Kidney Dis; 2003 Jan; 41(1):238-43. PubMed ID: 12500243
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 21.