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Journal Abstract Search

145 related items for PubMed ID: 2437795

  • 21. Regional assignment of the erythropoietin gene to human chromosome region 7pter----q22.
    Watkins PC, Eddy R, Hoffman N, Stanislovitis P, Beck AK, Galli J, Vellucci V, Gusella JF, Shows TB.
    Cytogenet Cell Genet; 1986; 42(4):214-8. PubMed ID: 2875851
    [Abstract] [Full Text] [Related]

  • 22. A highly polymorphic locus on chromosome 16q revealed by a probe from a chromosome-specific cosmid library.
    Bufton L, Mohandas TK, Magenis RE, Sheehy R, Bestwick RK, Litt M.
    Hum Genet; 1986 Dec; 74(4):425-31. PubMed ID: 2878870
    [Abstract] [Full Text] [Related]

  • 23. D10S20, a previously unmapped RFLP (OS-3), is located on 10q near D10S4.
    Miki T, Nishisho I, Tateishi H, Chen Y, Kidd JR, Wu J, Pravtcheva D, Pakstis AJ, Takai S, Ruddle FH.
    Genomics; 1988 Jul; 3(1):78-81. PubMed ID: 2906046
    [Abstract] [Full Text] [Related]

  • 24. Repetitive DNA (TGGA)n 5' to the human myelin basic protein gene: a new form of oligonucleotide repetitive sequence showing length polymorphism.
    Boylan KB, Ayres TM, Popko B, Takahashi N, Hood LE, Prusiner SB.
    Genomics; 1990 Jan; 6(1):16-22. PubMed ID: 1689270
    [Abstract] [Full Text] [Related]

  • 25. Four restriction fragment length polymorphisms revealed by probes from a single cosmid map to chromosome 19.
    Bufton L, Bruns GA, Magenis RE, Tomar D, Shaw D, Brook D, Litt M.
    Am J Hum Genet; 1986 Apr; 38(4):447-60. PubMed ID: 3010711
    [Abstract] [Full Text] [Related]

  • 26. Highly polymorphic DNA sequences in the distal region of the long arm of human chromosome 18.
    Müller U, Donlon TA, Harris P, Rose E, Hoffman E, Bruns GP, Latt SA.
    Cytogenet Cell Genet; 1987 Apr; 45(1):16-20. PubMed ID: 2885151
    [Abstract] [Full Text] [Related]

  • 27. Heparin cofactor II: cDNA sequence, chromosome localization, restriction fragment length polymorphism, and expression in Escherichia coli.
    Blinder MA, Marasa JC, Reynolds CH, Deaven LL, Tollefsen DM.
    Biochemistry; 1988 Jan 26; 27(2):752-9. PubMed ID: 2894851
    [Abstract] [Full Text] [Related]

  • 28. A new biallelic DNA polymorphism of the human COL5A1 gene.
    Cappa F, Caridi G, Gimelli G, Ghiggeri GM.
    Hum Genet; 1995 May 26; 95(5):599-600. PubMed ID: 7759090
    [Abstract] [Full Text] [Related]

  • 29. A DNA polymorphism in close physical linkage with the proopiomelanocortin gene.
    Feder J, Migone N, Chang AC, Cochet M, Cohen SN, Cann H, Cavalli-Sforza LL.
    Am J Hum Genet; 1983 Nov 26; 35(6):1090-6. PubMed ID: 6316780
    [Abstract] [Full Text] [Related]

  • 30. Isolation and regional localization of DNA segments revealing polymorphic loci from human chromosome 13.
    Cavenee W, Leach R, Mohandas T, Pearson P, White R.
    Am J Hum Genet; 1984 Jan 26; 36(1):10-24. PubMed ID: 6320640
    [Abstract] [Full Text] [Related]

  • 31. Three genes for enzymes of the pyruvate dehydrogenase complex map to human chromosomes 3, 7, and X.
    Olson S, Song BJ, Huh TL, Chi YT, Veech RL, McBride OW.
    Am J Hum Genet; 1990 Feb 26; 46(2):340-9. PubMed ID: 1967901
    [Abstract] [Full Text] [Related]

  • 32. Ferritin H gene polymorphism in idiopathic hemochromatosis.
    David V, Papadopoulos P, Yaouanq J, Blayau M, Abel L, Zappone E, Perichon M, Drysdale J, Le Gall JY, Simon M.
    Hum Genet; 1989 Jan 26; 81(2):123-6. PubMed ID: 2563249
    [Abstract] [Full Text] [Related]

  • 33. Localization of the coagulation factor XIII B subunit gene (F13B) to chromosome bands 1q31-32.1 and restriction fragment length polymorphism at the locus.
    Webb GC, Coggan M, Ichinose A, Board PG.
    Hum Genet; 1989 Jan 26; 81(2):157-60. PubMed ID: 2563250
    [Abstract] [Full Text] [Related]

  • 34. The X chromosome shows less genetic variation at restriction sites than the autosomes.
    Hofker MH, Skraastad MI, Bergen AA, Wapenaar MC, Bakker E, Millington-Ward A, van Ommen GJ, Pearson PL.
    Am J Hum Genet; 1986 Oct 26; 39(4):438-51. PubMed ID: 2876629
    [Abstract] [Full Text] [Related]

  • 35. Molecular genetic analysis of myelin-deficient mice: shiverer mutant mice show deletion in gene(s) coding for myelin basic protein.
    Kimura M, Inoko H, Katsuki M, Ando A, Sato T, Hirose T, Takashima H, Inayama S, Okano H, Takamatsu K.
    J Neurochem; 1985 Mar 26; 44(3):692-6. PubMed ID: 2579195
    [Abstract] [Full Text] [Related]

  • 36. Isolation and analysis of DNA markers specific to human chromosome 15.
    Tasset DM, Hartz JA, Kao FT.
    Am J Hum Genet; 1988 Jun 26; 42(6):854-66. PubMed ID: 2897161
    [Abstract] [Full Text] [Related]

  • 37. Mapping of a restriction fragment length polymorphism within the human aldolase B gene.
    Paolella G, Santamaria R, Buono P, Salvatore F.
    Hum Genet; 1987 Oct 26; 77(2):115-7. PubMed ID: 2888717
    [Abstract] [Full Text] [Related]

  • 38. Isolation and analysis of DNA marker revealing restriction fragment length polymorphism from X chromosome specific DNA library.
    Sadakane Y.
    Fukuoka Igaku Zasshi; 1989 Aug 26; 80(8):404-15. PubMed ID: 2573569
    [Abstract] [Full Text] [Related]

  • 39. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy.
    Johnson KJ, Jones PJ, Spurr N, Nimmo E, Davies J, Creed H, Weiss M, Williamson R.
    Cytogenet Cell Genet; 1988 Aug 26; 48(1):13-5. PubMed ID: 2460293
    [Abstract] [Full Text] [Related]

  • 40. Relationship of restriction fragment length polymorphisms (RFLP) at the bovine calpastatin locus to calpastatin activity and meat tenderness.
    Lonergan SM, Ernst CW, Bishop MD, Calkins CR, Koohmaraie M.
    J Anim Sci; 1995 Dec 26; 73(12):3608-12. PubMed ID: 8655434
    [Abstract] [Full Text] [Related]

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