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Journal Abstract Search

172 related items for PubMed ID: 1969227

  • 21. 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; 42(6):877-83. PubMed ID: 2897163
    [Abstract] [Full Text] [Related]

  • 22. 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; 93():309-17. PubMed ID: 1362280
    [No Abstract] [Full Text] [Related]

  • 23. Genetic haplotyping of ataxia-telangiectasia families localizes the major gene to an approximately 850 kb region on chromosome 11q23.1.
    Gatti RA, Lange E, Rotman G, Chen X, Uhrhammer N, Liang T, Chiplunkar S, Yang L, Udar N, Dandekar S, Sheikhavandi S, Wang Z, Yang HM, Polikow J, Elashoff M, Teletar M, Sanal O, Chessa L, McConville C, Taylor M, Shiloh Y, Porras O, Borresen AL, Wegner RD, Curry C, Gerken S, Lange K, Concannon P.
    Int J Radiat Biol; 1994 Dec; 66(6 Suppl):S57-62. PubMed ID: 7836853
    [Abstract] [Full Text] [Related]

  • 24. A pulsed-field gel electrophoresis map in the ataxia-telangiectasia region of chromosome 11q22.3.
    Uhrhammer N, Concannon P, Huo Y, Nakamura Y, Gatti RA.
    Genomics; 1994 Mar 15; 20(2):278-80. PubMed ID: 8020976
    [Abstract] [Full Text] [Related]

  • 25. Ataxia-telangiectasia: linkage analysis in highly inbred Arab and Druze families and differentiation from an ataxia-microcephaly-cataract syndrome.
    Ziv Y, Frydman M, Lange E, Zelnik N, Rotman G, Julier C, Jaspers NG, Dagan Y, Abeliovicz D, Dar H, Borochowitz Z, Lathrop M, Gatti RA, Shiloh Y.
    Hum Genet; 1992 Mar 15; 88(6):619-26. PubMed ID: 1551665
    [Abstract] [Full Text] [Related]

  • 26. Physical and genetic mapping at the ATA/ATC locus on chromosome 11q22-23.
    Rotman G, Savitski K, Vanagaite L, Bar-Shira A, Ziv Y, Gilad S, Uchenik V, Smith S, Shiloh Y.
    Int J Radiat Biol; 1994 Dec 15; 66(6 Suppl):S63-6. PubMed ID: 7836854
    [Abstract] [Full Text] [Related]

  • 27. Genetic mapping of nine DNA markers in the q11----q22 region of the human X chromosome.
    Arveiler B, Oberlé I, Mandel JL.
    Genomics; 1987 Sep 15; 1(1):60-6. PubMed ID: 2889662
    [Abstract] [Full Text] [Related]

  • 28. 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]

  • 29. Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1.
    Hyland VJ, Suthers GK, Friend K, MacKinnon RN, Callen DF, Breuning MH, Keith T, Brown VA, Phipps P, Sutherland GR.
    Hum Genet; 1990 Feb 15; 84(3):286-8. PubMed ID: 1968038
    [Abstract] [Full Text] [Related]

  • 30. Absence of linkage to the ataxia telangiectasia locus in familial breast cancer.
    Wooster R, Ford D, Mangion J, Ponder BA, Peto J, Easton DF, Stratton MR.
    Hum Genet; 1993 Aug 15; 92(1):91-4. PubMed ID: 8365732
    [Abstract] [Full Text] [Related]

  • 31. Physical localization of microsatellite markers at the ataxia-telangiectasia locus at 11q22-q23.
    Vanagaite L, Savitsky K, Rotman G, Ziv Y, Gerken SC, White R, Weissenbach J, Gillett G, Benham FJ, Richard CW, James MR, Collins FS, Shiloh Y.
    Genomics; 1994 Jul 01; 22(1):231-3. PubMed ID: 7959777
    [Abstract] [Full Text] [Related]

  • 32. The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.
    Hanauer A, Chery M, Fujita R, Driesel AJ, Gilgenkrantz S, Mandel JL.
    Am J Hum Genet; 1990 Jan 01; 46(1):133-7. PubMed ID: 2294745
    [Abstract] [Full Text] [Related]

  • 33. Linkage analyses of five chromosome 4 markers localizes the facioscapulohumeral muscular dystrophy (FSHD) gene to distal 4q35.
    Weiffenbach B, Bagley R, Falls K, Hyser C, Storvick D, Jacobsen SJ, Schultz P, Mendell J, Willems van Dijk K, Milner EC.
    Am J Hum Genet; 1992 Aug 01; 51(2):416-23. PubMed ID: 1642240
    [Abstract] [Full Text] [Related]

  • 34. Genetic mapping of four DNA markers (DXS16, DXS43, DXS85, and DXS143) from the p22 region of the human X chromosome.
    Brown CJ, Mahtani MM, Willard HF.
    Hum Genet; 1988 Nov 01; 80(3):296-8. PubMed ID: 3192218
    [Abstract] [Full Text] [Related]

  • 35. 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 Nov 01; 67(2):86-93. PubMed ID: 7913678
    [Abstract] [Full Text] [Related]

  • 36. Paired STSs amplified from radiation hybrids, and from associated YACs, identify highly polymorphic loci flanking the ataxia telangiectasia locus on chromosome 11q22-23.
    McConville CM, Byrd PJ, Ambrose HJ, Stankovic T, Ziv Y, Bar-Shira A, Vanagaite L, Rotman G, Shiloh Y, Gillett GT.
    Hum Mol Genet; 1993 Jul 01; 2(7):969-74. PubMed ID: 8364579
    [Abstract] [Full Text] [Related]

  • 37. Refined mapping of the psoriasin gene S100A7 to chromosome 1cen-q21.
    Børglum AD, Flint T, Madsen P, Celis JE, Kruse TA.
    Hum Genet; 1995 Nov 01; 96(5):592-6. PubMed ID: 8530009
    [Abstract] [Full Text] [Related]

  • 38. The CEPH consortium linkage map of human chromosome 2.
    Spurr NK, Cox S, Bryant SP, Attwood J, Robson EB, Shields DC, Steinbrueck T, Jenkins T, Murray JC, Kidd KK.
    Genomics; 1992 Dec 01; 14(4):1055-63. PubMed ID: 1478647
    [Abstract] [Full Text] [Related]

  • 39. A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.
    Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S.
    Am J Hum Genet; 1990 Jun 01; 46(6):1073-81. PubMed ID: 1971149
    [Abstract] [Full Text] [Related]

  • 40. The CEPH consortium linkage map of human chromosome 16.
    Kozman HM, Keith TP, Donis-Keller H, White RL, Weissenbach J, Dean M, Vergnaud G, Kidd K, Gusella J, Royle NJ.
    Genomics; 1995 Jan 01; 25(1):44-58. PubMed ID: 7774955
    [Abstract] [Full Text] [Related]

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