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Journal Abstract Search

56 related items for PubMed ID: 3471677

  • 21. Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions.
    Vocero-Akbani A, Helms C, Wang JC, Sanjurjo FJ, Korte-Sarfaty J, Veile RA, Liu L, Jauch A, Burgess AK, Hing AV, Holt MS, Ramachandra S, Whelan AJ, Anker R, Ahrent L, Chen M, Gavin MR, Iannantuoni K, Morton SM, Pandit SD, Read CM, Steinbrueck T, Warlick C, Smoller DA, Donis-Keller H.
    Genomics; 1996 Sep 15; 36(3):492-506. PubMed ID: 8884273
    [Abstract] [Full Text] [Related]

  • 22. Linkage analyses of human peptidase C (PEPC), human factor H (HF), and coagulation factor XIIIB (F13B).
    Kömpf J, Luckenbach C, Kloor D, Krczal D, Amorim A, Ritter H.
    Hum Genet; 1989 Aug 15; 83(1):97-8. PubMed ID: 2527799
    [Abstract] [Full Text] [Related]

  • 23. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
    [Abstract] [Full Text] [Related]

  • 24. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C.
    Nat Genet; 1994 Jan 26; 6(1):24-8. PubMed ID: 8136828
    [Abstract] [Full Text] [Related]

  • 25. Linkage analysis for age-related macular degeneration supports a gene on chromosome 10q26.
    Kenealy SJ, Schmidt S, Agarwal A, Postel EA, De La Paz MA, Pericak-Vance MA, Haines JL.
    Mol Vis; 2004 Jan 26; 10():57-61. PubMed ID: 14758336
    [Abstract] [Full Text] [Related]

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  • 27. Cystic fibrosis; hint of linkage with F13B.
    Eiberg H, Schmiegelow K, Koch C, Mohr J, Schwartz M, Niebuhr E.
    Clin Genet; 1985 Feb 26; 27(2):206. PubMed ID: 3856494
    [No Abstract] [Full Text] [Related]

  • 28. Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees.
    Christensen GB, Camp NJ, Farnham JM, Cannon-Albright LA.
    Prostate; 2007 May 01; 67(6):605-13. PubMed ID: 17299800
    [Abstract] [Full Text] [Related]

  • 29. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ, Blair IP, Liu Z, Fullerton JM, Scimone A, Van Herten M, Evans MR, Kirkby KC, Donald JA, Mitchell PB, Schofield PR.
    Mol Psychiatry; 2009 May 01; 14(5):492-500. PubMed ID: 18227837
    [Abstract] [Full Text] [Related]

  • 30. First-stage autosomal genome screen in extended pedigrees suggests genes predisposing to low bone mineral density on chromosomes 1p, 2p and 4q.
    Devoto M, Shimoya K, Caminis J, Ott J, Tenenhouse A, Whyte MP, Sereda L, Hall S, Considine E, Williams CJ, Tromp G, Kuivaniemi H, Ala-Kokko L, Prockop DJ, Spotila LD.
    Eur J Hum Genet; 1998 May 01; 6(2):151-7. PubMed ID: 9781060
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  • 33. The gene for coagulation factor XIII a subunit (F13A) is distal to HLA on chromosome 6.
    Board PG, Reid M, Serjeantson S.
    Hum Genet; 1984 May 01; 67(4):406-8. PubMed ID: 6149187
    [Abstract] [Full Text] [Related]

  • 34. Lack of close linkage between human coagulation factor F13A and HLA class I molecules.
    Schweighofer B, Wank R.
    Immunogenetics; 1989 May 01; 30(1):58-9. PubMed ID: 2568337
    [No Abstract] [Full Text] [Related]

  • 35.
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  • 36. Linkage between the loci for mitochondrial malic enzyme (ME2) and coagulation factor XIIIA subunit (F13A).
    Kömpf J, Schunter F, Wernet P, Ritter H.
    Hum Genet; 1985 May 01; 70(1):43-4. PubMed ID: 2860058
    [Abstract] [Full Text] [Related]

  • 37. The human obesity gene map: the 1996 update.
    Pérusse L, Chagnon YC, Dionne FT, Bouchard C.
    Obes Res; 1997 Jan 01; 5(1):49-61. PubMed ID: 9061716
    [Abstract] [Full Text] [Related]

  • 38. An alternative modality for the immunodetection of the molecular phenotypes of coagulation factor XIIIB.
    Cameselle FD, Caeiro B, Riveiro A.
    Hum Hered; 1993 Jan 01; 43(4):257-60. PubMed ID: 8344671
    [Abstract] [Full Text] [Related]

  • 39. Physical linkage of the human genes coding for complement factor H and coagulation factor XIII B subunit.
    Rey-Campos J, Baeza-Sanz D, Rodriguez de Cordoba S.
    Genomics; 1990 Aug 01; 7(4):644-6. PubMed ID: 2143748
    [No Abstract] [Full Text] [Related]

  • 40. Genetic polymorphism of the B subunit of human coagulation factor XIII: another classification.
    Kera Y, Nishimukai H, Yamasawa K.
    Hum Genet; 1981 Aug 01; 59(4):360-4. PubMed ID: 6949857
    [No Abstract] [Full Text] [Related]

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