These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

82 related items for PubMed ID: 8325642

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Dinucleotide repeat loci contribute highly informative genetic markers to the human chromosome 2 linkage map.
    Todd S, Sherman SL, Naylor SL.
    Genomics; 1993 Jun; 16(3):612-8. PubMed ID: 8100800
    [Abstract] [Full Text] [Related]

  • 6. Carrier detection of Werner's syndrome using a microsatellite that exhibits linkage disequilibrium with the Werner's syndrome locus.
    Kihara K, Nakura J, Ye L, Mitsuda N, Kamino K, Zhao Y, Fujioka Y, Miki T, Ogihara T.
    Jpn J Hum Genet; 1994 Dec; 39(4):403-9. PubMed ID: 7873752
    [Abstract] [Full Text] [Related]

  • 7. Close linkage of the gene for Werner's syndrome to ANK1 and D8S87 on the short arm of chromosome 8.
    Nakura J, Miki T, Nagano K, Kihara K, Ye L, Kamino K, Fujiwara Y, Yoshida S, Murano S, Fukuchi K.
    Gerontology; 1993 Dec; 39 Suppl 1():11-5. PubMed ID: 8365666
    [Abstract] [Full Text] [Related]

  • 8. Homozygosity mapping of the Werner syndrome locus (WRN).
    Nakura J, Wijsman EM, Miki T, Kamino K, Yu CE, Oshima J, Fukuchi K, Weber JL, Piussan C, Melaragno MI.
    Genomics; 1994 Oct; 23(3):600-8. PubMed ID: 7851888
    [Abstract] [Full Text] [Related]

  • 9. Genetic linkage of Werner's syndrome to five markers on chromosome 8.
    Goto M, Rubenstein M, Weber J, Woods K, Drayna D.
    Nature; 1992 Feb 20; 355(6362):735-8. PubMed ID: 1741060
    [Abstract] [Full Text] [Related]

  • 10. A new betaA1-crystallin splice junction mutation in autosomal dominant cataract.
    Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA.
    Invest Ophthalmol Vis Sci; 2000 Oct 20; 41(11):3278-85. PubMed ID: 11006214
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4.
    Murray JC, Bennett SR, Kwitek AE, Small KW, Schinzel A, Alward WL, Weber JL, Bell GI, Buetow KH.
    Nat Genet; 1992 Sep 20; 2(1):46-9. PubMed ID: 1303248
    [Abstract] [Full Text] [Related]

  • 13. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug 20; 43(8):2540-5. PubMed ID: 12147582
    [Abstract] [Full Text] [Related]

  • 14. A complex bilateral polysyndactyly disease locus maps to chromosome 7q36.
    Tsukurov O, Boehmer A, Flynn J, Nicolai JP, Hamel BC, Traill S, Zaleske D, Mankin HJ, Yeon H, Ho C.
    Nat Genet; 1994 Mar 20; 6(3):282-6. PubMed ID: 8012391
    [Abstract] [Full Text] [Related]

  • 15. A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
    Bateman JB, Richter L, Flodman P, Burch D, Brown S, Penrose P, Paul O, Geyer DD, Brooks DG, Spence MA.
    Invest Ophthalmol Vis Sci; 2006 Aug 20; 47(8):3441-9. PubMed ID: 16877414
    [Abstract] [Full Text] [Related]

  • 16. Excess of rare cancers in Werner syndrome (adult progeria).
    Goto M, Miller RW, Ishikawa Y, Sugano H.
    Cancer Epidemiol Biomarkers Prev; 1996 Apr 20; 5(4):239-46. PubMed ID: 8722214
    [Abstract] [Full Text] [Related]

  • 17. A 2.8 megabase YAC contig spanning D8S339, which is tightly linked to the Werner syndrome locus.
    Bruskiewich R, Schertzer M, Wood S.
    Genome; 1997 Feb 20; 40(1):77-83. PubMed ID: 9061915
    [Abstract] [Full Text] [Related]

  • 18. A 37-marker PCR-based genetic linkage map of human chromosome 9: observations on mutations and positive interference.
    Zahn LM, Kwiatkowski DJ.
    Genomics; 1995 Jul 20; 28(2):140-6. PubMed ID: 8530019
    [Abstract] [Full Text] [Related]

  • 19. Polymorphic SSR (simple-sequence-repeat) markers for chromosome 20.
    Melis R, Bradley P, Elsner T, Robertson M, Lawrence E, Gerken S, Albertsen H, White R.
    Genomics; 1993 Apr 20; 16(1):56-62. PubMed ID: 8486385
    [Abstract] [Full Text] [Related]

  • 20. A high-resolution linkage map of human 9q34.1.
    Henske EP, Ozelius L, Gusella JF, Haines JL, Kwiatkowski DJ.
    Genomics; 1993 Sep 20; 17(3):587-91. PubMed ID: 8244374
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.