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Journal Abstract Search

331 related items for PubMed ID: 2908534

  • 1. Restriction fragment length polymorphism (RFLP): applications in human chromosome mapping and genetic disease research.
    Watkins PC.
    Biotechniques; 1988 Apr; 6(4):310-9, 322. PubMed ID: 2908534
    [No Abstract] [Full Text] [Related]

  • 2.
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  • 3. One large kindred excludes a locus for multiple endocrine neoplasia type 2A from about 25% of the human autosomal genetic map.
    Pakstis AJ, Kidd JR, Castiglione CM, Pletcher BA, Murphy PD, Farrer LA, Genel M, Kidd KK.
    Henry Ford Hosp Med J; 1987 Apr; 35(2-3):164-7. PubMed ID: 2891651
    [No Abstract] [Full Text] [Related]

  • 4. DNA markers for the cystic fibrosis locus.
    O'Connell P, Leppert M, Nakamura Y, Dean M, Park M, Vande Woude G, Farrall M, Wainwright B, Williamson R, Lathrop GM.
    Prog Clin Biol Res; 1987 Apr; 254():127-37. PubMed ID: 2893384
    [No Abstract] [Full Text] [Related]

  • 5. A candidate for the cystic fibrosis locus isolated by selection for methylation-free islands.
    Estivill X, Farrall M, Scambler PJ, Bell GM, Hawley KM, Lench NJ, Bates GP, Kruyer HC, Frederick PA, Stanier P.
    Nature; 1987 Apr; 326(6116):840-5. PubMed ID: 2883581
    [Abstract] [Full Text] [Related]

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  • 7. Mapping human chromosomes.
    White RL.
    Harvey Lect; 1987 Apr; 80():67-87. PubMed ID: 6400657
    [No Abstract] [Full Text] [Related]

  • 8. Diagnosis of genetic disease by linkage analysis.
    Cann HM, Cohen D, Dausset J.
    Birth Defects Orig Artic Ser; 1987 Apr; 23(2):33-60. PubMed ID: 2885042
    [No Abstract] [Full Text] [Related]

  • 9. Attempts to identify the chromosomal localization of the Friedreich's ataxia locus.
    Chamberlain S, Worrall C, Williamson R.
    Adv Neurol; 1988 Apr; 48():257-60. PubMed ID: 2891256
    [No Abstract] [Full Text] [Related]

  • 10. The application of molecular genetics to the study of the basic defect causing cystic fibrosis.
    Estivill X, Bates G, Bell G, Farrall M, Frederick P, Hawley K, Kruyer H, Lench N, Scrambler P, Stanier P.
    Prog Clin Biol Res; 1987 Apr; 254():181-90. PubMed ID: 2893385
    [Abstract] [Full Text] [Related]

  • 11. The clinical applications of DNA polymorphisms.
    Thein SL, Wainscoat JS.
    Dis Markers; 1986 Oct; 4(3):203-18. PubMed ID: 2898316
    [No Abstract] [Full Text] [Related]

  • 12. Where is the locus for multiple endocrine neoplasia type 2A?
    Simpson NE, Kidd KK.
    Henry Ford Hosp Med J; 1987 Oct; 35(2-3):168-71. PubMed ID: 2891652
    [No Abstract] [Full Text] [Related]

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  • 14. Molecular genetic strategies to investigate Huntington's disease.
    Gilliam TC, Gusella JF, Lehrach H.
    Adv Neurol; 1988 Oct; 48():17-29. PubMed ID: 2891255
    [No Abstract] [Full Text] [Related]

  • 15. Multipoint mapping and linkage based upon affected pedigree members--Genetic Analysis Workshop 6. Proceedings of a workshop. Long Beach, Mississippi, October 10-12, 1988.
    Prog Clin Biol Res; 1989 Oct; 329():1-218. PubMed ID: 2622934
    [No Abstract] [Full Text] [Related]

  • 16. Critics denounce first genome map as premature.
    Barinaga M.
    Nature; 1989 Oct; 329(6140):571. PubMed ID: 2889146
    [No Abstract] [Full Text] [Related]

  • 17. Applications of restriction fragment length polymorphism.
    Narayanan S.
    Ann Clin Lab Sci; 1991 Oct; 21(4):291-6. PubMed ID: 1677556
    [Abstract] [Full Text] [Related]

  • 18. A variance component approach to dichotomous trait linkage analysis using a threshold model.
    Duggirala R, Williams JT, Williams-Blangero S, Blangero J.
    Genet Epidemiol; 1997 Oct; 14(6):987-92. PubMed ID: 9433612
    [Abstract] [Full Text] [Related]

  • 19. Cartilage-hair hypoplasia gene assigned to chromosome 9 by linkage analysis.
    Sulisalo T, Sistonen P, Hästbacka J, Wadelius C, Mäkitie O, de la Chapelle A, Kaitila I.
    Nat Genet; 1993 Apr; 3(4):338-41. PubMed ID: 7981754
    [Abstract] [Full Text] [Related]

  • 20. The Diego blood group locus is located on chromosome 17q.
    Zelinski T, Coghlan G, White L, Philipps S.
    Genomics; 1993 Sep; 17(3):665-6. PubMed ID: 7902326
    [Abstract] [Full Text] [Related]

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