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 *

119 related articles for article (PubMed ID: 10868217)

  • 1. DFNA3.
    Denoyelle F; Weil D; Levilliers J; Petit C
    Adv Otorhinolaryngol; 2000; 56():78-83. PubMed ID: 10868217
    [No Abstract]   [Full Text] [Related]  

  • 2. Mapping of the DFNB1 locus.
    Mueller RF; Lench NJ
    Adv Otorhinolaryngol; 2000; 56():116-23. PubMed ID: 10868223
    [No Abstract]   [Full Text] [Related]  

  • 3. Connexin 26 gene linked to a dominant deafness.
    Denoyelle F; Lina-Granade G; Plauchu H; Bruzzone R; Chaïb H; Lévi-Acobas F; Weil D; Petit C
    Nature; 1998 May; 393(6683):319-20. PubMed ID: 9620796
    [No Abstract]   [Full Text] [Related]  

  • 4. 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]  

  • 5. Connexin 26 gene mutation and autosomal recessive deafness.
    Reardon W
    Lancet; 1998 Feb; 351(9100):383-4. PubMed ID: 9482285
    [No Abstract]   [Full Text] [Related]  

  • 6. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss.
    Kelley PM; Harris DJ; Comer BC; Askew JW; Fowler T; Smith SD; Kimberling WJ
    Am J Hum Genet; 1998 Apr; 62(4):792-9. PubMed ID: 9529365
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families.
    Maestrini E; Korge BP; Ocaña-Sierra J; Calzolari E; Cambiaghi S; Scudder PM; Hovnanian A; Monaco AP; Munro CS
    Hum Mol Genet; 1999 Jul; 8(7):1237-43. PubMed ID: 10369869
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation.
    Antoniadi T; Pampanos A; Petersen MB
    Prenat Diagn; 2001 Jan; 21(1):10-3. PubMed ID: 11180233
    [TBL] [Abstract][Full Text] [Related]  

  • 10. High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim.
    Sobe T; Erlich P; Berry A; Korostichevsky M; Vreugde S; Avraham KB; Bonné-Tamir B; Shohat M
    Am J Med Genet; 1999 Oct; 86(5):499-500. PubMed ID: 10508996
    [No Abstract]   [Full Text] [Related]  

  • 11. Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East.
    Shahin H; Walsh T; Sobe T; Lynch E; King MC; Avraham KB; Kanaan M
    Hum Genet; 2002 Mar; 110(3):284-9. PubMed ID: 11935342
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations.
    Carrasquillo MM; Zlotogora J; Barges S; Chakravarti A
    Hum Mol Genet; 1997 Nov; 6(12):2163-72. PubMed ID: 9328482
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rapid detection of the 35delG mutation in the GJB2 gene in childhood deafness.
    Tessa A; Patrono C; Santorelli FM; Giannotti A; Digilio MC; Pacifico C; Presuttari F; Tieri L
    J Med Screen; 2000; 7(3):167. PubMed ID: 11126168
    [No Abstract]   [Full Text] [Related]  

  • 14. Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11-->q12 and mouse chromosome 14D1-E1 by in situ hybridization.
    Mignon C; Fromaget C; Mattei MG; Gros D; Yamasaki H; Mesnil M
    Cytogenet Cell Genet; 1996; 72(2-3):185-6. PubMed ID: 8978770
    [No Abstract]   [Full Text] [Related]  

  • 15. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness.
    Kelsell DP; Dunlop J; Stevens HP; Lench NJ; Liang JN; Parry G; Mueller RF; Leigh IM
    Nature; 1997 May; 387(6628):80-3. PubMed ID: 9139825
    [TBL] [Abstract][Full Text] [Related]  

  • 16. W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness.
    Tekin M; Arnos KS; Xia XJ; Oelrich MK; Liu XZ; Nance WE; Pandya A
    Clin Genet; 2001 Apr; 59(4):269-73. PubMed ID: 11298683
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Maternal origin of a de novo mutation of the connexin 26 gene resulting in recessive nonsyndromic deafness.
    Shalev SA; Hujirat Y
    Am J Med Genet A; 2004 Feb; 124A(4):411-2. PubMed ID: 14735592
    [No Abstract]   [Full Text] [Related]  

  • 19. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2).
    Lench NJ; Markham AF; Mueller RF; Kelsell DP; Smith RJ; Willems PJ; Schatteman I; Capon H; Van De Heyning PJ; Van Camp G
    J Med Genet; 1998 Feb; 35(2):151-2. PubMed ID: 9507396
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.