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

502 related items for PubMed ID: 21822880

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27. High-throughput identification, database storage and analysis of SNPs in EST sequences.
    Useche FJ, Gao G, Harafey M, Rafalski A.
    Genome Inform; 2001; 12():194-203. PubMed ID: 11791238
    [Abstract] [Full Text] [Related]

  • 28. Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis.
    Hehir-Kwa JY, Egmont-Petersen M, Janssen IM, Smeets D, van Kessel AG, Veltman JA.
    DNA Res; 2007 Feb 28; 14(1):1-11. PubMed ID: 17363414
    [Abstract] [Full Text] [Related]

  • 29. Array-Based Comparative Genomic Hybridization (aCGH).
    Zhang C, Cerveira E, Romanovitch M, Zhu Q.
    Methods Mol Biol; 2017 Feb 28; 1541():167-179. PubMed ID: 27910023
    [Abstract] [Full Text] [Related]

  • 30.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 31. COKGEN: a software for the identification of rare copy number variation from SNP microarrays.
    Yavaş G, Koyutürk M, Ozsoyoğlu M, Gould MP, Laframboise T.
    Pac Symp Biocomput; 2010 Feb 28; ():371-82. PubMed ID: 19908389
    [Abstract] [Full Text] [Related]

  • 32. [Genome-wide detection of loss of heterozygosity and copy number variation in a human lung large cell carcinoma cell line by affymetrix single-nucleotide polymorphism array 500K.].
    Hu B, Chen J, Liu H, Wu H, Wu Z, Wang Y, Bai Y, Li Y, Zhou Q.
    Zhongguo Fei Ai Za Zhi; 2008 Jun 20; 11(3):327-32. PubMed ID: 20731928
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 35. Characterization of copy number-stable regions in the human genome.
    Johansson AC, Feuk L.
    Hum Mutat; 2011 Aug 20; 32(8):947-55. PubMed ID: 21542059
    [Abstract] [Full Text] [Related]

  • 36. Detection and characterization of copy number variation in autism spectrum disorder.
    Marshall CR, Scherer SW.
    Methods Mol Biol; 2012 Aug 20; 838():115-35. PubMed ID: 22228009
    [Abstract] [Full Text] [Related]

  • 37. Genome-wide detection of copy number variations using high-density SNP genotyping platforms in Holsteins.
    Jiang L, Jiang J, Yang J, Liu X, Wang J, Wang H, Ding X, Liu J, Zhang Q.
    BMC Genomics; 2013 Feb 27; 14():131. PubMed ID: 23442346
    [Abstract] [Full Text] [Related]

  • 38. A genome-wide scan for copy number variations using high-density single nucleotide polymorphism array in Simmental cattle.
    Wu Y, Fan H, Jing S, Xia J, Chen Y, Zhang L, Gao X, Li J, Gao H, Ren H.
    Anim Genet; 2015 Jun 27; 46(3):289-98. PubMed ID: 25917301
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Genomic structural diversity in Criollo Argentino horses: Analysis of copy number variations.
    Corbi-Botto CM, Morales-Durand H, Zappa ME, Sadaba SA, Peral-García P, Giovambattista G, Díaz S.
    Gene; 2019 May 05; 695():26-31. PubMed ID: 30763671
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 26.