Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination
We are sorry, but NCBI web applications do not support your browser and may not function properly. More information

    Results: 8

    1.

    Longitudinal study shows increasing obesity and hyperglycemia in micronesia.

    Murdock D, Salit J, Stoffel M, Friedman JM, Pe'er I, Breslow JL, Bonnen PE.

    Obesity (Silver Spring). 2012 Sep 18. doi: 10.1002/oby.20041. [Epub ahead of print]

    PMID:
    23404778
    [PubMed - as supplied by publisher]
    2.

    WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype.

    Bacino CA, Dhar SU, Brunetti-Pierri N, Lee B, Bonnen PE.

    Am J Med Genet A. 2012 Nov;158A(11):2917-24. doi: 10.1002/ajmg.a.35608. Epub 2012 Sep 17.

    PMID:
    22987818
    [PubMed - in process]
    3.

    WDR62 missense mutation in a consanguineous family with primary microcephaly.

    Bacino CA, Arriola LA, Wiszniewska J, Bonnen PE.

    Am J Med Genet A. 2012 Mar;158A(3):622-5. doi: 10.1002/ajmg.a.34417. Epub 2012 Feb 3.

    PMID:
    22308068
    [PubMed - indexed for MEDLINE]
    4.

    European admixture on the Micronesian island of Kosrae: lessons from complete genetic information.

    Bonnen PE, Lowe JK, Altshuler DM, Breslow JL, Stoffel M, Friedman JM, Pe'er I.

    Eur J Hum Genet. 2010 Mar;18(3):309-16. doi: 10.1038/ejhg.2009.180. Epub 2009 Oct 21.

    PMID:
    19844264
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    5.

    Haplotype and linkage disequilibrium architecture for human cancer-associated genes.

    Bonnen PE, Wang PJ, Kimmel M, Chakraborty R, Nelson DL.

    Genome Res. 2002 Dec;12(12):1846-53.

    PMID:
    12466288
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    6.

    Physical and genetic characterization reveals a pseudogene, an evolutionary junction, and unstable loci in distal Xq28.

    Aradhya S, Woffendin H, Bonnen P, Heiss NS, Yamagata T, Esposito T, Bardaro T, Poustka A, D'Urso M, Kenwrick S, Nelson DL.

    Genomics. 2002 Jan;79(1):31-40.

    PMID:
    11827455
    [PubMed - indexed for MEDLINE]
    7.

    Haplotypes at ATM identify coding-sequence variation and indicate a region of extensive linkage disequilibrium.

    Bonnen PE, Story MD, Ashorn CL, Buchholz TA, Weil MM, Nelson DL.

    Am J Hum Genet. 2000 Dec;67(6):1437-51. Epub 2000 Nov 14.

    PMID:
    11078475
    [PubMed - indexed for MEDLINE]
    Free PMC Article
    8.

    Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.

    Zhuchenko O, Bailey J, Bonnen P, Ashizawa T, Stockton DW, Amos C, Dobyns WB, Subramony SH, Zoghbi HY, Lee CC.

    Nat Genet. 1997 Jan;15(1):62-9.

    PMID:
    8988170
    [PubMed - indexed for MEDLINE]

      Display Settings:

      Format
      Items per page
      Sort by

      Send to:

      Choose Destination

      Supplemental Content

      Find related data

      Search details

      See more...

      Recent activity

      Write to the Help Desk