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 *

92 related articles for article (PubMed ID: 9482285)

  • 21. [Genetic deafness].
    Vincent C
    Rev Med Interne; 2011 Jun; 32 Suppl 1():S2-4. PubMed ID: 21549459
    [No Abstract]   [Full Text] [Related]  

  • 22. The architecture of hearing.
    Pennisi E
    Science; 1997 Nov; 278(5341):1223-4. PubMed ID: 9411747
    [No Abstract]   [Full Text] [Related]  

  • 23. Deafness. Sounds from the cochlea.
    Avraham KB
    Nature; 1997 Dec; 390(6660):559-60. PubMed ID: 9403680
    [No Abstract]   [Full Text] [Related]  

  • 24. Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus.
    Grifa A; Wagner CA; D'Ambrosio L; Melchionda S; Bernardi F; Lopez-Bigas N; Rabionet R; Arbones M; Monica MD; Estivill X; Zelante L; Lang F; Gasparini P
    Nat Genet; 1999 Sep; 23(1):16-8. PubMed ID: 10471490
    [No Abstract]   [Full Text] [Related]  

  • 25. Molecular diagnosis of genetic deafness.
    Jonard L; Marlin S; Louha M; Bonnet C; Couderc R; Garabedian N; Denoyelle F;
    Clin Biochem; 2011 May; 44(7):510-511. PubMed ID: 22036352
    [No Abstract]   [Full Text] [Related]  

  • 26. Possible modifier effects of keratin 17 gene mutation on keratitis-ichthyosis-deafness syndrome.
    Natsuga K; Shinkuma S; Kanda M; Suzuki Y; Chosa N; Narita Y; Setoyama M; Nishie W; Akiyama M; Shimizu H
    Br J Dermatol; 2012 Apr; 166(4):903-5. PubMed ID: 21999526
    [No Abstract]   [Full Text] [Related]  

  • 27. Selection for deafness?
    Meyer CG; Amedofu GK; Brandner JM; Pohland D; Timmann C; Horstmann RD
    Nat Med; 2002 Dec; 8(12):1332-3. PubMed ID: 12457154
    [No Abstract]   [Full Text] [Related]  

  • 28. Connexin mutations and hearing loss.
    Scott DA; Kraft ML; Stone EM; Sheffield VC; Smith RJ
    Nature; 1998 Jan; 391(6662):32. PubMed ID: 9422505
    [No Abstract]   [Full Text] [Related]  

  • 29. Deafness genes.
    Kitamura K; Takahashi K; Tamagawa Y; Noguchi Y; Kuroishikawa Y; Ishikawa K; Hagiwara H
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Connexin 26 mutations: the first practical genetic marker of inherited hearing loss.
    Perry CF
    Med J Aust; 2001 Aug; 175(4):182-3. PubMed ID: 11587274
    [No Abstract]   [Full Text] [Related]  

  • 31. Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.
    Meng M; Li X; Ge H; Chen F; Han M; Zhang Y; Kang D; Xie W; Gao Z; Pan X; Dai P; Chi F; Chen S; Liu P; Zhang C; Cao J; Jiang H; Xu X; Wang W; Duan T
    Genet Med; 2014 Dec; 16(12):972-6. PubMed ID: 24830326
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Gene symbol: GJB2.
    Matos T; Caria H; Teixeira H; Fialho G
    Hum Genet; 2007 Apr; 121(2):298. PubMed ID: 17598246
    [No Abstract]   [Full Text] [Related]  

  • 33. Genetic screening for deafness.
    Smith RJ; Hone S
    Pediatr Clin North Am; 2003 Apr; 50(2):315-29. PubMed ID: 12809325
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Deafness and mutations in the connexin 26 gene.
    Zlotogora J
    N Engl J Med; 1999 Apr; 340(16):1288. PubMed ID: 10215495
    [No Abstract]   [Full Text] [Related]  

  • 35. Screening for mutations in the GJB3 gene in Brazilian patients with nonsyndromic deafness.
    Alexandrino F; Oliveira CA; Reis FC; Maciel-Guerra AT; Sartorato EL
    J Appl Genet; 2004; 45(2):249-54. PubMed ID: 15131355
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Molecular mechanism of a frequent genetic form of deafness.
    Michel V; Hardelin JP; Petit C
    N Engl J Med; 2003 Aug; 349(7):716-7. PubMed ID: 12917317
    [No Abstract]   [Full Text] [Related]  

  • 37. Impact of genetic counseling and Connexin-26 and Connexin-30 testing on deaf identity and comprehension of genetic test results in a sample of deaf adults: a prospective, longitudinal study.
    Palmer CG; Boudreault P; Baldwin EE; Sinsheimer JS
    PLoS One; 2014; 9(11):e111512. PubMed ID: 25375116
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Re: Pediatric otolaryngologists' use of genetic testing.
    Welsh LW; Welsh JJ
    Ann Otol Rhinol Laryngol; 2007 Aug; 116(8):637-8. PubMed ID: 17847733
    [No Abstract]   [Full Text] [Related]  

  • 39. Genetic testing to identify deaf newborns.
    Green GE; Smith RJ; Bent JP; Cohn ES
    JAMA; 2000 Sep; 284(10):1245. PubMed ID: 10979110
    [No Abstract]   [Full Text] [Related]  

  • 40. Motors, channels and the sounds of silence.
    Avraham KB
    Nat Med; 1997 Jun; 3(6):608-9. PubMed ID: 9176483
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.