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Journal Abstract Search

145 related items for PubMed ID: 680701

  • 21. Lods and some phase-known information for chromosome 6 loci GLO, Ch, and HLA-A, -B, and -D.
    Lewis M, Kaita H, Philipps S, Giblett ER, Anderson JE, Schroeder ML, Pellett F.
    Cytogenet Cell Genet; 1978; 22(1-6):415-7. PubMed ID: 752515
    [No Abstract] [Full Text] [Related]

  • 22. Mapping of the linkage group GLO--Bf--HLA-B,C,A--PGM3. 2. Segregation analysis.
    Schunter F, Wernet P, Kömpf J, Bissbort S, Göhler F.
    Hum Genet; 1978 Nov 16; 44(3):321-31. PubMed ID: 730170
    [Abstract] [Full Text] [Related]

  • 23. On regional mapping of human chromosome 6. Review and own findings.
    Bender K, Bissbort S, Hiller C, Mayerova A, Wienker TF.
    Acta Anthropogenet; 1983 Nov 16; 7(2):85-105. PubMed ID: 6234899
    [Abstract] [Full Text] [Related]

  • 24. Analysis for linkage between F13A and three chromosome 6 marker loci: evidence for 6pter:F13A:HLA:GLO1:cen gene order.
    Wong P, Komarnicki L, Schroeder ML, Lewis M, Kaita H, Philipps S, Stranc L, McAlpine PJ.
    Hum Genet; 1988 Jul 16; 79(3):228-30. PubMed ID: 2900213
    [Abstract] [Full Text] [Related]

  • 25. The locus for glyoxalase I (GLO) is between HLA-A and PGM3 on chromosome 6 of man.
    Meera Khan P, Volkers WS, Doppert BA, Bijnen AB, Schreuder I, Van Rood JJ.
    Birth Defects Orig Artic Ser; 1976 Jul 16; 12(7):328-30. PubMed ID: 1024634
    [No Abstract] [Full Text] [Related]

  • 26. Properdin factor B (Bf) and glyoxalase in Graves' disease.
    Allannic H, Fauchet R, Lorcy Y, Phengsavath H, Gueguen M, Knoi TD, Genetet B, Le Gall JY.
    Acta Endocrinol (Copenh); 1983 Jan 16; 102(1):57-61. PubMed ID: 6572032
    [Abstract] [Full Text] [Related]

  • 27. A genetic linkage analysis of chromosome 6 markers Chido, HLA, and glyoxalase.
    Lewis M, Kaita H, Chown B, Bowen P, Lee CS, McDonald S, Giblett ER, Anderson J, Dossetor JB, Schlaut J, Pai KR, Singal DP, Steinberg AG.
    Birth Defects Orig Artic Ser; 1976 Jan 16; 12(7):317-21. PubMed ID: 1024632
    [No Abstract] [Full Text] [Related]

  • 28. Human red glyoxalase I polymorphism in the Swiss population: phenotype frequencies and a simplified technique.
    Pflugshaupt R, Scherz R, Bütler R.
    Hum Hered; 1978 Jan 16; 28(3):235-7. PubMed ID: 649180
    [No Abstract] [Full Text] [Related]

  • 29. A haplotype study of HLA complex with special reference to the HLA-DR series and to Bf. C2 and glyoxalase I polymorphisms.
    Dausset J, Legrand L, Lepage V, Contu L, Marcelli-Barge A, Wildloecher I, Benajam A, Meo T, Degos L.
    Tissue Antigens; 1978 Oct 16; 12(4):297-307. PubMed ID: 83027
    [Abstract] [Full Text] [Related]

  • 30. Possible assignment of the glyoxalase I (GLO) gene to chromosome 6 using man-mouse somatic cell hybrids.
    Bender K, Grzeschik KH.
    Hum Genet; 1976 Mar 12; 31(3):341-5. PubMed ID: 986362
    [Abstract] [Full Text] [Related]

  • 31. Glyoxalase 1: a possible 'null' allele.
    Rubinstein P, Suciu-Foca N.
    Hum Hered; 1979 Mar 12; 29(4):217-20. PubMed ID: 478555
    [Abstract] [Full Text] [Related]

  • 32. Gamma ray-induced loss of expression of HLA and glyoxalase I alleles in lymphoblastoid cells.
    Kavathas P, Bach FH, DeMars R.
    Proc Natl Acad Sci U S A; 1980 Jul 12; 77(7):4251-5. PubMed ID: 6933474
    [Abstract] [Full Text] [Related]

  • 33. Genetic susceptibility to diabetes mellitus: the distribution of properdin factor B (Bf) and glyoxalase (GLO) phenotypes.
    Kirk RL, Theophilus J, Whitehouse S, Court J, Zimmet P.
    Diabetes; 1979 Oct 12; 28(10):949-51. PubMed ID: 478186
    [Abstract] [Full Text] [Related]

  • 34. Family studies define a new histocompatibility locus, SB, between HLA-DR and GLO.
    Shaw S, Kavathas P, Pollack MS, Charmot D, Mawas C.
    Nature; 1981 Oct 29; 293(5835):745-7. PubMed ID: 6974826
    [No Abstract] [Full Text] [Related]

  • 35. Localization of the human GLO gene locus.
    Olaisen B, Gedde-Dahl T, Thorsby E.
    Hum Genet; 1976 Jun 29; 32(3):301-4. PubMed ID: 939550
    [Abstract] [Full Text] [Related]

  • 36. Joint phenotype distributions at the glyoxalase I and haptoglobin loci in Finland.
    Virtaranta-Knowles K, Nevanlinna HR.
    Hum Hered; 1987 Jun 29; 37(1):59-61. PubMed ID: 3557463
    [No Abstract] [Full Text] [Related]

  • 37. Possible linkage relationship between genetic markers and blood magnesium and zinc. A twin study.
    Darlu P, Defrise-Gussenhoven E, Michotte Y, Susanne C, Henrotte JG.
    Acta Genet Med Gemellol (Roma); 1985 Jun 29; 34(1-2):109-12. PubMed ID: 4050290
    [Abstract] [Full Text] [Related]

  • 38. HLA-A,B,C, Bf and glyoxalase I polymorphisms in a sample of the Kabyle population (Algeria).
    Bouali M, Dehay C, Benajam A, Poirier JC, Degos L, Marcelli-Barge A.
    Tissue Antigens; 1981 May 29; 17(5):501-6. PubMed ID: 7336415
    [Abstract] [Full Text] [Related]

  • 39. Gene linkage studies on glyoxalase I.
    Giblett ER, Lewis M.
    Cytogenet Cell Genet; 1976 May 29; 16(1-5):313. PubMed ID: 975897
    [No Abstract] [Full Text] [Related]

  • 40. GLO I and Bf phenotype distribution in a West German population sample.
    Mauff G, Wachauf P, Schaal KP, Pulverer G.
    Hum Hered; 1978 May 29; 28(6):431-4. PubMed ID: 680704
    [Abstract] [Full Text] [Related]

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