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Journal Abstract Search

186 related items for PubMed ID: 2787825

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  • 5. Rapid and sensitive nonradioactive detection of mutant K-ras genes via 'enriched' PCR amplification.
    Kahn SM, Jiang W, Culbertson TA, Weinstein IB, Williams GM, Tomita N, Ronai Z.
    Oncogene; 1991 Jun; 6(6):1079-83. PubMed ID: 1676837
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  • 7. Genetic diversity from a limited repertoire of mutations on different common allelic backgrounds: alpha 1-antitrypsin deficiency variant Pduarte.
    Hildesheim J, Kinsley G, Bissell M, Pierce J, Brantly M.
    Hum Mutat; 1993 Jun; 2(3):221-8. PubMed ID: 8364590
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  • 8. Polymerase chain reaction detection of S and Z alpha-1-antitrypsin variants by duplex PCR assay.
    Lucotte G, Sesboüé R.
    Mol Cell Probes; 1999 Oct; 13(5):389-91. PubMed ID: 10508561
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  • 12. Rapid DNA analysis of alpha 1-antitrypsin deficiency: application of an improved method for amplifying mutated gene sequences.
    Dermer SJ, Johnson EM.
    Lab Invest; 1988 Sep; 59(3):403-8. PubMed ID: 3261817
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  • 15. An improved method for prenatal diagnosis of genetic diseases by analysis of amplified DNA sequences. Application to hemophilia A.
    Kogan SC, Doherty M, Gitschier J.
    N Engl J Med; 1987 Oct 15; 317(16):985-90. PubMed ID: 3657865
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  • 16. Characterization of the sequence of the normal alpha-1-antitrypsin M3 allele and function of the M3 protein.
    Curiel D, Laubach V, Vogelmeier C, Wurts L, Crystal RG.
    Am J Respir Cell Mol Biol; 1989 Dec 15; 1(6):471-7. PubMed ID: 2637759
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  • 17. Denaturing gradient gel electrophoresis of the alpha 1-antitrypsin gene: application to prenatal diagnosis.
    Dubel JR, Finwick R, Hejtmancik JF.
    Am J Med Genet; 1991 Oct 01; 41(1):39-43. PubMed ID: 1951462
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  • 18. Prenatal diagnosis of alpha-1-antitrypsin deficiency using polymerase chain reaction (PCR). Comparison of conventional RFLP methods with PCR used in combination with allele specific oligonucleotides or RFLP analysis.
    Schwartz M, Petersen KB, Gregersen N, Hinkel K, Newton CR.
    Clin Genet; 1989 Dec 01; 36(6):419-26. PubMed ID: 2574085
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  • 19. [Analysis of alpha 1-antitrypsin deficiency using DNA methods].
    Wick U, Kühnl P, Engel W.
    Monatsschr Kinderheilkd; 1990 Aug 01; 138(8):438-42. PubMed ID: 2215506
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  • 20. PAP: detection of ultra rare mutations depends on P* oligonucleotides: "sleeping beauties" awakened by the kiss of pyrophosphorolysis.
    Liu Q, Sommer SS.
    Hum Mutat; 2004 May 01; 23(5):426-36. PubMed ID: 15108273
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