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Journal Abstract Search

143 related items for PubMed ID: 1980995

  • 1. Assignment of the polymorphic intestinal mucin gene (MUC2) to chromosome 11p15.
    Griffiths B, Matthews DJ, West L, Attwood J, Povey S, Swallow DM, Gum JR, Kim YS.
    Ann Hum Genet; 1990 Oct; 54(4):277-85. PubMed ID: 1980995
    [Abstract] [Full Text] [Related]

  • 2. Regional localization of the intestinal mucin gene MUC3 to chromosome 7q22.
    Fox MF, Lahbib F, Pratt W, Attwood J, Gum J, Kim Y, Swallow DM.
    Ann Hum Genet; 1992 Oct; 56(4):281-7. PubMed ID: 1362870
    [Abstract] [Full Text] [Related]

  • 3. Assignment of human tracheobronchial mucin gene(s) to 11p15 and a tracheobronchial mucin-related sequence to chromosome 13.
    Nguyen VC, Aubert JP, Gross MS, Porchet N, Degand P, Frézal J.
    Hum Genet; 1990 Dec; 86(2):167-72. PubMed ID: 2265829
    [Abstract] [Full Text] [Related]

  • 4. Human mucin genes assigned to 11p15.5: identification and organization of a cluster of genes.
    Pigny P, Guyonnet-Duperat V, Hill AS, Pratt WS, Galiegue-Zouitina S, d'Hooge MC, Laine A, Van-Seuningen I, Degand P, Gum JR, Kim YS, Swallow DM, Aubert JP, Porchet N.
    Genomics; 1996 Dec 15; 38(3):340-52. PubMed ID: 8975711
    [Abstract] [Full Text] [Related]

  • 5. Localization of the FGR protooncogene on the genetic linkage map of human chromosome 1p.
    Dracopoli NC, Stanger BZ, Lager M, Housman DE.
    Genomics; 1988 Aug 15; 3(2):124-8. PubMed ID: 2906322
    [Abstract] [Full Text] [Related]

  • 6. Allelic association and recombination hotspots in the mucin gene (MUC) complex on chromosome 11p15.5.
    Rousseau K, Byrne C, Griesinger G, Leung A, Chung A, Hill AS, Swallow DM.
    Ann Hum Genet; 2007 Sep 15; 71(Pt 5):561-9. PubMed ID: 17535267
    [Abstract] [Full Text] [Related]

  • 7. The ataxia-telangiectasia gene (ATA) on chromosome II is distinct from the ETS-1 gene.
    Concannon P, Malhotra U, Charmley P, Reynolds J, Lange K, Gatti RA.
    Am J Hum Genet; 1990 Apr 15; 46(4):789-94. PubMed ID: 1969227
    [Abstract] [Full Text] [Related]

  • 8. Variable number tandem repeat polymorphism of the mucin genes located in the complex on 11p15.5.
    Vinall LE, Hill AS, Pigny P, Pratt WS, Toribara N, Gum JR, Kim YS, Porchet N, Aubert JP, Swallow DM.
    Hum Genet; 1998 Mar 15; 102(3):357-66. PubMed ID: 9544852
    [Abstract] [Full Text] [Related]

  • 9. CEPH consortium map of chromosome 14.
    Cox DW, Billingsley GD, Bale AE, Donis-Keller H, Edwards JH, Litt M, Mcbride W, Persichetti F, Spurr NK, Weber JL.
    Cytogenet Cell Genet; 1995 Mar 15; 69(3-4):175-8. PubMed ID: 7698005
    [Abstract] [Full Text] [Related]

  • 10. A genetic linkage map of 32 loci on human chromosome 10.
    Bowden DW, Gravius TC, Green P, Falls K, Wurster-Hill D, Noll W, Müller-Kahle H, Donis-Keller H.
    Genomics; 1989 Nov 15; 5(4):718-26. PubMed ID: 2574142
    [Abstract] [Full Text] [Related]

  • 11. A primary genetic map of the pericentromeric region of the human X chromosome.
    Mahtani MM, Willard HF.
    Genomics; 1988 May 15; 2(4):294-301. PubMed ID: 2906040
    [Abstract] [Full Text] [Related]

  • 12. A genetic linkage map of 27 loci from PND to FY on the short arm of human chromosome I.
    Dracopoli NC, Stanger BZ, Ito CY, Call KM, Lincoln SE, Lander ES, Housman DE.
    Am J Hum Genet; 1988 Oct 15; 43(4):462-70. PubMed ID: 2902785
    [Abstract] [Full Text] [Related]

  • 13. Characterization of the human mucin gene MUC5AC: a consensus cysteine-rich domain for 11p15 mucin genes?
    Guyonnet Duperat V, Audie JP, Debailleul V, Laine A, Buisine MP, Galiegue-Zouitina S, Pigny P, Degand P, Aubert JP, Porchet N.
    Biochem J; 1995 Jan 01; 305 ( Pt 1)(Pt 1):211-9. PubMed ID: 7826332
    [Abstract] [Full Text] [Related]

  • 14. Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH database. Centre d'Etude de Polymorphisme Humain.
    Westbrook CA, Le Beau MM, Neuman WL, Keinanen M, Yamaoka LH, Speer MC, Espinosa R, Nakamura Y, Williamson R, Mullan M.
    Cytogenet Cell Genet; 1994 Jan 01; 67(2):86-93. PubMed ID: 7913678
    [Abstract] [Full Text] [Related]

  • 15. The human skeletal muscle adenine nucleotide translocator gene maps to chromosome 4q35 in the region of the facioscapulohumeral muscular dystrophy locus.
    Wijmenga C, Winokur ST, Padberg GW, Skraastad MI, Altherr MR, Wasmuth JJ, Murray JC, Hofker MH, Frants RR.
    Hum Genet; 1993 Sep 01; 92(2):198-203. PubMed ID: 8103757
    [Abstract] [Full Text] [Related]

  • 16. Regional assignment of the human acid sphingomyelinase gene (SMPD1) by PCR analysis of somatic cell hybrids and in situ hybridization to 11p15.1----p15.4.
    da Veiga Pereira L, Desnick RJ, Adler DA, Disteche CM, Schuchman EH.
    Genomics; 1991 Feb 01; 9(2):229-34. PubMed ID: 2004772
    [Abstract] [Full Text] [Related]

  • 17. Assignment of 112 microsatellite markers to 23 chromosome 11 subregions delineated by somatic hybrids: comparison with the genetic map.
    Couillin P, Le Guern E, Vignal A, Fizames C, Ravisé N, Delportes D, Reguigne I, Rosier MF, Junien C, van Heyningen V.
    Genomics; 1994 May 15; 21(2):379-87. PubMed ID: 8088833
    [Abstract] [Full Text] [Related]

  • 18. A microsatellite genetic linkage map of human chromosome 13.
    Petrukhin KE, Speer MC, Cayanis E, Bonaldo MF, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J.
    Genomics; 1993 Jan 15; 15(1):76-85. PubMed ID: 8432553
    [Abstract] [Full Text] [Related]

  • 19. Extensive DNA polymorphism at the factor XIIIa (F13A) locus and linkage to HLA.
    Zoghbi HY, Daiger SP, McCall A, O'Brien WE, Beaudet AL.
    Am J Hum Genet; 1988 Jun 15; 42(6):877-83. PubMed ID: 2897163
    [Abstract] [Full Text] [Related]

  • 20. The use of linkage analysis and the Centre d'Etude Polymorphisme Humain (CEPH) panel of DNA in the study of the arginine vasopressin, oxytocin and prodynorphin gene loci.
    Summar ML.
    Prog Brain Res; 1992 Jun 15; 93():309-17. PubMed ID: 1362280
    [No Abstract] [Full Text] [Related]

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