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189 related items for PubMed ID: 8808282

  • 1. Narrowing the genetic interval and yeast artificial chromosome map in the branchio-oto-renal region on chromosome 8q.
    Kumar S, Kimberling WJ, Lanyi A, Sumegi J, Pinnt J, Ing P, Tinley S, Marres HA, Cremers CW.
    Genomics; 1996 Jan 01; 31(1):71-9. PubMed ID: 8808282
    [Abstract] [Full Text] [Related]

  • 2. Detection of a megabase deletion in a patient with branchio-oto-renal syndrome (BOR) and tricho-rhino-phalangeal syndrome (TRPS): implications for mapping and cloning the BOR gene.
    Gu JZ, Wagner MJ, Haan EA, Wells DE.
    Genomics; 1996 Jan 15; 31(2):201-6. PubMed ID: 8824802
    [Abstract] [Full Text] [Related]

  • 3. Localization of branchio-oto-renal (BOR) syndrome to a 3 Mb region of chromosome 8q.
    Wang Y, Treat K, Schroer RJ, O'Brien JE, Stevenson RE, Schwartz CE.
    Am J Med Genet; 1994 Jun 01; 51(2):169-75. PubMed ID: 8092198
    [Abstract] [Full Text] [Related]

  • 4. Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).
    Stratakis CA, Lin JP, Rennert OM.
    Am J Med Genet; 1998 Sep 23; 79(3):209-14. PubMed ID: 9788564
    [Abstract] [Full Text] [Related]

  • 5. Characterization of a translocation-associated deletion defines the candidate region for the gene responsible for branchio-oto-renal syndrome.
    Kalatzis V, Abdelhak S, Compain S, Vincent C, Petit C.
    Genomics; 1996 Jun 15; 34(3):422-5. PubMed ID: 8786145
    [Abstract] [Full Text] [Related]

  • 6. Refining the region of branchio-oto-renal syndrome and defining the flanking markers on chromosome 8q by genetic mapping.
    Kumar S, Kimberling WJ, Connolly CJ, Tinley S, Marres HA, Cremers CW.
    Am J Hum Genet; 1994 Dec 15; 55(6):1188-94. PubMed ID: 7977379
    [Abstract] [Full Text] [Related]

  • 7. Refined localization of the branchiootorenal syndrome gene by linkage and haplotype analysis.
    Ni L, Wagner MJ, Kimberling WJ, Pembrey ME, Grundfast KM, Kumar S, Daiger SP, Wells DE, Johnson K, Smith RJ.
    Am J Med Genet; 1994 Jun 01; 51(2):176-84. PubMed ID: 8092199
    [Abstract] [Full Text] [Related]

  • 8. Autosomal-dominant branchio-otic (BO) syndrome is not allelic to the branchio-oto-renal (BOR) gene at 8q13.
    Kumar S, Marres HA, Cremers CW, Kimberling WJ.
    Am J Med Genet; 1998 Apr 13; 76(5):395-401. PubMed ID: 9556298
    [Abstract] [Full Text] [Related]

  • 9. A 2-Mb YAC contig and physical map covering the chromosome 8q12 breakpoint cluster region in pleomorphic adenomas of the salivary glands.
    Kas K, Röijer E, Voz M, Meyen E, Stenman G, Van de Ven WJ.
    Genomics; 1997 Aug 01; 43(3):349-58. PubMed ID: 9268638
    [Abstract] [Full Text] [Related]

  • 10. A physical and transcript map based upon refinement of the critical interval for PPH1, a gene for familial primary pulmonary hypertension. The International PPH Consortium.
    Machado RD, Pauciulo MW, Fretwell N, Veal C, Thomson JR, Vilariño Güell C, Aldred M, Brannon CA, Trembath RC, Nichols WC.
    Genomics; 2000 Sep 01; 68(2):220-8. PubMed ID: 10964520
    [Abstract] [Full Text] [Related]

  • 11. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
    Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, Seemayer TA, Klein G, Purtilo DT, Sumegi J.
    Genomics; 1997 Jan 01; 39(1):55-65. PubMed ID: 9027486
    [Abstract] [Full Text] [Related]

  • 12. The human B22 subunit of the NADH-ubiquinone oxidoreductase maps to the region of chromosome 8 involved in branchio-oto-renal syndrome.
    Gu JZ, Lin X, Wells DE.
    Genomics; 1996 Jul 01; 35(1):6-10. PubMed ID: 8661098
    [Abstract] [Full Text] [Related]

  • 13. Genetic aspects of the BOR syndrome--branchial fistulas, ear pits, hearing loss, and renal anomalies.
    Fraser FC, Ling D, Clogg D, Nogrady B.
    Am J Med Genet; 1978 Jul 01; 2(3):241-52. PubMed ID: 263442
    [Abstract] [Full Text] [Related]

  • 14. A high-density STS map based on a single contig of YAC and P1 clones in the chromosome 8p12-p21 region.
    Mitsuda N, Nakura J, Ye L, Zhao Y, Fujioka Y, Takahashi-Fujii A, Ishino Y, Kato I, Hashimoto K, Ogihara T, Miki T.
    Genomics; 1997 Apr 01; 41(1):49-55. PubMed ID: 9126481
    [Abstract] [Full Text] [Related]

  • 15. Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q.
    Haan EA, Hull YJ, White S, Cockington R, Charlton P, Callen DF.
    Am J Med Genet; 1989 Apr 01; 32(4):490-4. PubMed ID: 2773990
    [Abstract] [Full Text] [Related]

  • 16. An EST and STS-based YAC contig map of human chromosome 9q22.3.
    Lench NJ, Telford EA, Andersen SE, Moynihan TP, Robinson PA, Markham AF.
    Genomics; 1996 Dec 01; 38(2):199-205. PubMed ID: 8954802
    [Abstract] [Full Text] [Related]

  • 17. Phenotypic manifestations of branchio-oto-renal syndrome.
    Chen A, Francis M, Ni L, Cremers CW, Kimberling WJ, Sato Y, Phelps PD, Bellman SC, Wagner MJ, Pembrey M.
    Am J Med Genet; 1995 Sep 25; 58(4):365-70. PubMed ID: 8533848
    [Abstract] [Full Text] [Related]

  • 18. Mapping of the locus for autosomal dominant amelogenesis imperfecta (AIH2) to a 4-Mb YAC contig on chromosome 4q11-q21.
    Kärrman C, Bäckman B, Dixon M, Holmgren G, Forsman K.
    Genomics; 1997 Jan 15; 39(2):164-70. PubMed ID: 9027503
    [Abstract] [Full Text] [Related]

  • 19. Physical mapping of the rippling muscle disease locus.
    Stephan DA, Hoffman EP.
    Genomics; 1999 Feb 01; 55(3):268-74. PubMed ID: 10049580
    [Abstract] [Full Text] [Related]

  • 20. Autosomal dominant branchio-oto-renal syndrome--localization of a disease gene to chromosome 8q by linkage in a Dutch family.
    Kumar S, Kimberling WJ, Kenyon JB, Smith RJ, Marres HA, Cremers CW.
    Hum Mol Genet; 1992 Oct 01; 1(7):491-5. PubMed ID: 1307249
    [Abstract] [Full Text] [Related]

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