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PUBMED FOR HANDHELDS

Journal Abstract Search


121 related items for PubMed ID: 2754309

  • 1. Diagnosis by gene amplification.
    Kazazian HH.
    J Lab Clin Med; 1989 Aug; 114(2):95-6. PubMed ID: 2754309
    [No Abstract] [Full Text] [Related]

  • 2. [Molecular biology in medicine. X. DNA chips].
    Gamba G.
    Rev Invest Clin; 1997 Aug; 49(4):339-42. PubMed ID: 9708001
    [No Abstract] [Full Text] [Related]

  • 3. [Basics of DNA diagnosis].
    Hayashi K.
    Tanpakushitsu Kakusan Koso; 1996 Nov; 41(15 Suppl):2478-83. PubMed ID: 8952412
    [No Abstract] [Full Text] [Related]

  • 4. Molecular basis of genetic disease and molecular methods.
    McPherson RA.
    Clin Lab Med; 1995 Dec; 15(4):779-94. PubMed ID: 8838223
    [Abstract] [Full Text] [Related]

  • 5. [Molecular genetics in the research and diagnosis of human pathology].
    Estivill Z, Nunes V, Gallano P.
    Med Clin (Barc); 1990 Apr 14; 94(14):541-7. PubMed ID: 1972429
    [No Abstract] [Full Text] [Related]

  • 6. Rapid, nonradioactive detection of mutations in the human genome by allele-specific amplification.
    Okayama H, Curiel DT, Brantly ML, Holmes MD, Crystal RG.
    J Lab Clin Med; 1989 Aug 14; 114(2):105-13. PubMed ID: 2787825
    [Abstract] [Full Text] [Related]

  • 7. Amplification methods in the molecular diagnosis of genetic diseases.
    Ben-Ezra JM.
    Clin Lab Med; 1995 Dec 14; 15(4):795-815. PubMed ID: 8838224
    [Abstract] [Full Text] [Related]

  • 8. [Amplification of trinucleotide repeats--a new mutation mechanism causing common genetic diseases].
    Shem-Tov N, Shohat M.
    Harefuah; 1994 Oct 14; 127(7-8):268-73. PubMed ID: 7813958
    [No Abstract] [Full Text] [Related]

  • 9. [DNA amplification and its application in medicine].
    Estivill X, Nunes V.
    Med Clin (Barc); 1991 Mar 09; 96(9):341-9. PubMed ID: 2046445
    [No Abstract] [Full Text] [Related]

  • 10. Real-time assays with molecular beacons and other fluorescent nucleic acid hybridization probes.
    Marras SA, Tyagi S, Kramer FR.
    Clin Chim Acta; 2006 Jan 09; 363(1-2):48-60. PubMed ID: 16111667
    [Abstract] [Full Text] [Related]

  • 11. [Genetic engineering for diagnosis].
    Nojima H.
    Rinsho Byori; 1985 Nov 09; 33 Spec No 65():37-48. PubMed ID: 2419604
    [No Abstract] [Full Text] [Related]

  • 12. Long-range jumping of incompletely extended polymerase chain fragments generates unexpected products.
    Huang LM, Jeang KT.
    Biotechniques; 1994 Feb 09; 16(2):242-4, 246. PubMed ID: 8179886
    [No Abstract] [Full Text] [Related]

  • 13. [First attempts in preimplantation genetic diagnosis: genetic analysis].
    Bán Z, Fancsovits P, Nagy B, Kamaszné HM, Urbancsek J, Papp Z.
    Orv Hetil; 2001 Nov 11; 142(45):2487-92. PubMed ID: 11778356
    [Abstract] [Full Text] [Related]

  • 14. [Management of the CNVs in constitutional human genetics using array CGH].
    Nemos C, Bursztejn AC, Jonveaux P.
    Pathol Biol (Paris); 2008 Sep 11; 56(6):354-61. PubMed ID: 18515018
    [Abstract] [Full Text] [Related]

  • 15. Strategies for preimplantation genetic diagnosis of single gene disorders by DNA amplification.
    Wells D, Sherlock JK.
    Prenat Diagn; 1998 Dec 11; 18(13):1389-401. PubMed ID: 9949439
    [Abstract] [Full Text] [Related]

  • 16. MLPA and MAPH: new techniques for detection of gene deletions.
    Sellner LN, Taylor GR.
    Hum Mutat; 2004 May 11; 23(5):413-9. PubMed ID: 15108271
    [Abstract] [Full Text] [Related]

  • 17. [Molecular basis of diagnosis in genetics].
    Longy M.
    Gastroenterol Clin Biol; 2001 Apr 11; 25(4 Suppl):B14-7. PubMed ID: 11449139
    [No Abstract] [Full Text] [Related]

  • 18. The use of cloned gene probes to diagnose human genetic disease.
    Williamson R, Moore G, Johnson K.
    Rev Med Brux; 1987 Apr 11; 8(4):240-1. PubMed ID: 3589275
    [No Abstract] [Full Text] [Related]

  • 19. [Use of DNA polymorphism in the diagnosis of human genetic diseases].
    Cebrat S.
    Postepy Hig Med Dosw; 1988 Apr 11; 42(5):461-82. PubMed ID: 2908211
    [No Abstract] [Full Text] [Related]

  • 20. How to find a mutation behind an inherited disease.
    Peltonen L, Pulkkinen L.
    Ann Clin Res; 1986 Apr 11; 18(5-6):224-30. PubMed ID: 2882725
    [Abstract] [Full Text] [Related]


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