BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

185 related articles for article (PubMed ID: 11073537)

  • 1. Characterisation and genetic mapping of a new X linked deafness syndrome.
    Martin DM; Probst FJ; Camper SA; Petty EM
    J Med Genet; 2000 Nov; 37(11):836-41. PubMed ID: 11073537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L; Schwartz C; Eriksen H; Andreasson S; Ponjavic V; Dahl A; Stevenson RE; May M; Arena F; Barker D
    J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.
    del Castillo I; Villamar M; Sarduy M; Romero L; Herraiz C; Hernández FJ; Rodríguez M; Borrás I; Montero A; Bellón J; Tapia MC; Moreno F
    Hum Mol Genet; 1996 Sep; 5(9):1383-7. PubMed ID: 8872482
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Refinement of the locus for non-syndromic sensorineural deafness (DFN2).
    Cui B; Zhang H; Lu Y; Zhong W; Pei G; Kong X; Hu L
    J Genet; 2004 Apr; 83(1):35-8. PubMed ID: 15240907
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Identification of a new locus for autosomal dominant non-syndromic hearing impairment (DFNA7) in a large Norwegian family.
    Fagerheim T; Nilssen O; Raeymaekers P; Brox V; Moum T; Elverland HH; Teig E; Omland HH; Fostad GK; Tranebjaerg L
    Hum Mol Genet; 1996 Aug; 5(8):1187-91. PubMed ID: 8842739
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Molecular characterization of a novel X-linked syndrome involving developmental delay and deafness.
    Hildebrand MS; de Silva MG; Tan TY; Rose E; Nishimura C; Tolmachova T; Hulett JM; White SM; Silver J; Bahlo M; Smith RJ; Dahl HH
    Am J Med Genet A; 2007 Nov; 143A(21):2564-75. PubMed ID: 17935254
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.
    Coyle B; Coffey R; Armour JA; Gausden E; Hochberg Z; Grossman A; Britton K; Pembrey M; Reardon W; Trembath R
    Nat Genet; 1996 Apr; 12(4):421-3. PubMed ID: 8630497
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mapping of DFN2 to Xq22.
    Tyson J; Bellman S; Newton V; Simpson P; Malcolm S; Pembrey ME; Bitner-Glindzicz M
    Hum Mol Genet; 1996 Dec; 5(12):2055-60. PubMed ID: 8968763
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
    Manolis EN; Eavey RD; Sangwatanaroj S; Halpin C; Rosenbaum S; Watkins H; Jarcho J; Seidman CE; Seidman JG
    Am J Otol; 1999 Sep; 20(5):621-6. PubMed ID: 10503584
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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]  

  • 14. Clinical and genetic heterogeneity in X-linked deafness.
    Reardon W; Middleton-Price HR; Malcolm S; Phelps P; Bellman S; Luxon L; Martin JA; Bumby A; Pembrey ME
    Br J Audiol; 1992 Apr; 26(2):109-14. PubMed ID: 1628115
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness.
    Mustapha M; Salem N; Weil D; el-Zir E; Loiselet J; Petit C
    Eur J Hum Genet; 1998; 6(6):548-51. PubMed ID: 9887371
    [TBL] [Abstract][Full Text] [Related]  

  • 16. A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.
    Lalwani AK; Brister JR; Fex J; Grundfast KM; Pikus AT; Ploplis B; San Agustin T; Skarka H; Wilcox ER
    Am J Hum Genet; 1994 Oct; 55(4):685-94. PubMed ID: 7942846
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Genetic aspects of deafness].
    Dallapiccola B; Mingarelli R; Gennarelli M; Novelli G
    Acta Otorhinolaryngol Ital; 1996 Apr; 16(2):79-90. PubMed ID: 8766069
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenotype and genotype analysis of a Chinese family with prelingual X-linked hereditary hearing impairment.
    Han B; Cheng J; Yang SZ; Cao JY; Shen WD; Ji F; Kang DY; Zhang X; Dai P; Yuan HJ
    Chin Med J (Engl); 2009 Apr; 122(7):830-3. PubMed ID: 19493398
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel locus for autosomal dominant non-syndromic hearing loss, DFNA31, maps to chromosome 6p21.3.
    Snoeckx RL; Kremer H; Ensink RJ; Flothmann K; de Brouwer A; Smith RJ; Cremers CW; Van Camp G
    J Med Genet; 2004 Jan; 41(1):11-3. PubMed ID: 14729819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
    Mustapha M; Chouery E; Torchard-Pagnez D; Nouaille S; Khrais A; Sayegh FN; Mégarbané A; Loiselet J; Lathrop M; Petit C; Weil D
    Hum Genet; 2002 Apr; 110(4):348-50. PubMed ID: 11941484
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.