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PUBMED FOR HANDHELDS

Journal Abstract Search


189 related items for PubMed ID: 12271815

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2. DNA diagnosis by capillary electrophoresis and microfabricated electrophoretic devices.
    Qin J, Fung Y, Lin B.
    Expert Rev Mol Diagn; 2003 May; 3(3):387-94. PubMed ID: 12779012
    [Abstract] [Full Text] [Related]

  • 3. Miniaturization of molecular biological techniques for gene assay.
    Lien KY, Lee GB.
    Analyst; 2010 Jul; 135(7):1499-518. PubMed ID: 20390199
    [Abstract] [Full Text] [Related]

  • 4. DNA mutation detection and analysis using miniaturized microfluidic systems.
    Handal MI, Ugaz VM.
    Expert Rev Mol Diagn; 2006 Jan; 6(1):29-38. PubMed ID: 16359265
    [Abstract] [Full Text] [Related]

  • 5. DNA sequencing and genotyping in miniaturized electrophoresis systems.
    Kan CW, Fredlake CP, Doherty EA, Barron AE.
    Electrophoresis; 2004 Nov; 25(21-22):3564-88. PubMed ID: 15565709
    [Abstract] [Full Text] [Related]

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  • 7. Mutation detection using fluorescent hybridization probes and melting curve analysis.
    Lyon E.
    Expert Rev Mol Diagn; 2001 May; 1(1):92-101. PubMed ID: 11901805
    [Abstract] [Full Text] [Related]

  • 8. MEMS-based sample preparation for molecular diagnostics.
    Huang Y, Mather EL, Bell JL, Madou M.
    Anal Bioanal Chem; 2002 Jan; 372(1):49-65. PubMed ID: 11939213
    [Abstract] [Full Text] [Related]

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  • 10. Molecular testing for hereditary hemochromatosis.
    Liang Q, Lichy JH.
    Expert Rev Mol Diagn; 2002 Jan; 2(1):49-59. PubMed ID: 11963802
    [Abstract] [Full Text] [Related]

  • 11. A new technology for mutation detection.
    Shackelford W, Deng S, Murayama K, Wang J.
    Ann N Y Acad Sci; 2004 Jun; 1022():257-62. PubMed ID: 15251970
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  • 13. Parallel molecular genetic analysis.
    McKenzie SE, Mansfield E, Rappaport E, Surrey S, Fortina P.
    Eur J Hum Genet; 1998 Jun; 6(5):417-29. PubMed ID: 9801865
    [Abstract] [Full Text] [Related]

  • 14. [Detection of point mutation in p53 gene by capillary electrophoresis-PCR-SSCP analysis].
    Liu J, Jing H, Ru Q, Deng Y, Luo G, Huang Q.
    Sichuan Da Xue Xue Bao Yi Xue Ban; 2003 Jul; 34(3):476-9. PubMed ID: 12910694
    [Abstract] [Full Text] [Related]

  • 15. Cycling gradient capillary electrophoresis: a low-cost tool for high-throughput analysis of genetic variations.
    Minarik M, Minarikova L, Bjørheim J, Ekstrøm PO.
    Electrophoresis; 2003 Jun; 24(11):1716-22. PubMed ID: 12783447
    [Abstract] [Full Text] [Related]

  • 16. BRCA1 mutation screening using restriction endonuclease fingerprinting-single-strand conformation polymorphism in an automated capillary electrophoresis system.
    Kringen P, Egedal S, Pedersen JC, Harbitz TB, Tveit KM, Berg K, Børresen-Dale AL, Andersen TI.
    Electrophoresis; 2002 Dec; 23(24):4085-91. PubMed ID: 12481264
    [Abstract] [Full Text] [Related]

  • 17. Analysis of 65 tuberous sclerosis complex (TSC) patients by TSC2 DGGE, TSC1/TSC2 MLPA, and TSC1 long-range PCR sequencing, and report of 28 novel mutations.
    Rendtorff ND, Bjerregaard B, Frödin M, Kjaergaard S, Hove H, Skovby F, Brøndum-Nielsen K, Schwartz M, Danish Tuberous Sclerosis Group.
    Hum Mutat; 2005 Oct; 26(4):374-83. PubMed ID: 16114042
    [Abstract] [Full Text] [Related]

  • 18. Serial processing of biological reactions using flow-through microfluidic devices: coupled PCR/LDR for the detection of low-abundant DNA point mutations.
    Hashimoto M, Barany F, Xu F, Soper SA.
    Analyst; 2007 Sep; 132(9):913-21. PubMed ID: 17710267
    [Abstract] [Full Text] [Related]

  • 19. Miniaturised nucleic acid analysis.
    Auroux PA, Koc Y, deMello A, Manz A, Day PJ.
    Lab Chip; 2004 Dec; 4(6):534-46. PubMed ID: 15570362
    [Abstract] [Full Text] [Related]

  • 20. Evaluation of a multicapillary electrophoresis instrument for mitochondrial DNA typing.
    Stewart JE, Aagaard PJ, Pokorak EG, Polanskey D, Budowle B.
    J Forensic Sci; 2003 May; 48(3):571-80. PubMed ID: 12762527
    [Abstract] [Full Text] [Related]


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