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

75 related items for PubMed ID: 18972372

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

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Automating sequence-based detection and genotyping of SNPs from diploid samples.
    Stephens M, Sloan JS, Robertson PD, Scheet P, Nickerson DA.
    Nat Genet; 2006 Mar; 38(3):375-81. PubMed ID: 16493422
    [Abstract] [Full Text] [Related]

  • 10. Fluorescent sequencing for heterozygote mutation detection.
    Graham CA, Hill AJ.
    Methods Mol Biol; 2001 Mar; 167():193-213. PubMed ID: 11265316
    [No Abstract] [Full Text] [Related]

  • 11. Reliable identification of large numbers of candidate SNPs from public EST data.
    Buetow KH, Edmonson MN, Cassidy AB.
    Nat Genet; 1999 Mar; 21(3):323-5. PubMed ID: 10080189
    [Abstract] [Full Text] [Related]

  • 12. Base-calling of automated sequencer traces using phred. II. Error probabilities.
    Ewing B, Green P.
    Genome Res; 1998 Mar; 8(3):186-94. PubMed ID: 9521922
    [Abstract] [Full Text] [Related]

  • 13. Automating resequencing-based detection of insertion-deletion polymorphisms.
    Bhangale TR, Stephens M, Nickerson DA.
    Nat Genet; 2006 Dec; 38(12):1457-62. PubMed ID: 17115056
    [Abstract] [Full Text] [Related]

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

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Automated splicing mutation analysis by information theory.
    Nalla VK, Rogan PK.
    Hum Mutat; 2005 Apr; 25(4):334-42. PubMed ID: 15776446
    [Abstract] [Full Text] [Related]

  • 17. High throughput DNA sequence variant detection by conformation sensitive capillary electrophoresis and automated peak comparison.
    Davies H, Dicks E, Stephens P, Cox C, Teague J, Greenman C, Bignell G, O'meara S, Edkins S, Parker A, Stevens C, Menzies A, Blow M, Bottomley B, Dronsfield M, Futreal PA, Stratton MR, Wooster R.
    Genomics; 2006 Mar; 87(3):427-32. PubMed ID: 16406726
    [Abstract] [Full Text] [Related]

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

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 4.