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

263 related items for PubMed ID: 11149487

  • 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. Linkage of Paget disease of bone to a novel region on human chromosome 18q23.
    Good DA, Busfield F, Fletcher BH, Duffy DL, Kesting JB, Andersen J, Shaw JT.
    Am J Hum Genet; 2002 Feb; 70(2):517-25. PubMed ID: 11742440
    [Abstract] [Full Text] [Related]

  • 6. Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity study.
    McNairn JD, Damron TA, Landas SK, Ambrose JL, Shrimpton AE.
    J Mol Diagn; 2001 Nov; 3(4):171-7. PubMed ID: 11687601
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8. Genome-wide scan of exfoliation syndrome.
    Lemmelä S, Forsman E, Sistonen P, Eriksson A, Forsius H, Järvelä I.
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4136-42. PubMed ID: 17724198
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
    Wilson SG, Adam G, Langdown M, Reneland R, Braun A, Andrew T, Surdulescu GL, Norberg M, Dudbridge F, Reed PW, Sambrook PN, Kleyn PW, Spector TD.
    Eur J Hum Genet; 2006 Mar; 14(3):340-8. PubMed ID: 16391564
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome.
    Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B.
    Mov Disord; 2006 Jan; 21(1):28-33. PubMed ID: 16124010
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Analysis of environmental factors in familial versus sporadic Paget's disease of bone--the New England Registry for Paget's Disease of Bone.
    Seton M, Choi HK, Hansen MF, Sebaldt RJ, Cooper C.
    J Bone Miner Res; 2003 Aug; 18(8):1519-24. PubMed ID: 12929942
    [Abstract] [Full Text] [Related]

  • 20. Genetic linkage of familial expansile osteolysis to chromosome 18q.
    Hughes AE, Shearman AM, Weber JL, Barr RJ, Wallace RG, Osterberg PH, Nevin NC, Mollan RA.
    Hum Mol Genet; 1994 Feb; 3(2):359-61. PubMed ID: 7911698
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 14.