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Journal Abstract Search

93 related items for PubMed ID: 8789447

  • 41. Screening for mutations in the GH-1 gene by dideoxy fingerprinting (ddF).
    Miyata I, Eto Y, Kamijo T, Ogawa M, Futrakul A, Phillips JA.
    Endocr J; 1999 Mar; 46 Suppl():S71-4. PubMed ID: 12054125
    [No Abstract] [Full Text] [Related]

  • 42. Screening the dopamine D1 receptor gene in 131 schizophrenics and eight alcoholics: identification of polymorphisms but lack of functionally significant sequence changes.
    Liu Q, Sobell JL, Heston LL, Sommer SS.
    Am J Med Genet; 1995 Apr 24; 60(2):165-71. PubMed ID: 7485254
    [Abstract] [Full Text] [Related]

  • 43. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug 24; 56(3):105-52. PubMed ID: 19728970
    [Abstract] [Full Text] [Related]

  • 44. The D5 dopamine receptor gene in schizophrenia: identification of a nonsense change and multiple missense changes but lack of association with disease.
    Sobell JL, Lind TJ, Sigurdson DC, Zald DH, Snitz BE, Grove WM, Heston LL, Sommer SS.
    Hum Mol Genet; 1995 Apr 24; 4(4):507-14. PubMed ID: 7633397
    [Abstract] [Full Text] [Related]

  • 45. Development of standard reference materials for diagnosis of p53 mutations: analysis by slab gel single strand conformation polymorphism.
    O'Connell CD, Tian J, Juhasz A, Wenz HM, Atha DH.
    Electrophoresis; 1998 Feb 24; 19(2):164-71. PubMed ID: 9548275
    [Abstract] [Full Text] [Related]

  • 46. Rapid identification of single nucleotide polymorphisms by fluorescence-based capillary electrophoresis.
    Bernat M, Titos E, Clària J.
    Genet Mol Res; 2002 Mar 31; 1(1):72-8. PubMed ID: 14963815
    [Abstract] [Full Text] [Related]

  • 47. Dideoxyfingerprinting (ddF) analysis of the type X collagen gene (COL10A1) and identification of a novel mutation (S671P) in a kindred with Schmid metaphyseal chondrodysplasia.
    Stratakis CA, Orban Z, Burns AL, Vottero A, Mitsiades CS, Marx SJ, Abbassi V, Chrousos GP.
    Biochem Mol Med; 1996 Dec 31; 59(2):112-7. PubMed ID: 8986632
    [Abstract] [Full Text] [Related]

  • 48. Direct genomic multiplex PCR for BRCA1 and application to mutation detection by single-strand conformation and heteroduplex analysis.
    Barker DF.
    Hum Mutat; 2000 Oct 31; 16(4):334-44. PubMed ID: 11013444
    [Abstract] [Full Text] [Related]

  • 49. A rapid fluorescence based multiplex polymerase chain reaction--single-strand conformation polymorphism method for p53 mutation detection.
    Berggren P, Steineck G, Hemminki K.
    Electrophoresis; 2000 Jul 31; 21(12):2335-42. PubMed ID: 10939443
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  • 52. [A rapid and simple detection of DNA fragment with point mutation by capillary electrophoresis].
    Jing H, Liu J, Ru Q, Deng Y, Luo G, Huang Q.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2001 Aug 31; 18(4):317-21. PubMed ID: 11484177
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  • 55. Screening of differentially amplified cDNA products from RNA arbitrarily primed PCR fingerprints using single strand conformation polymorphism (SSCP) gels.
    Mathieu-Daudé F, Cheng R, Welsh J, McClelland M.
    Nucleic Acids Res; 1996 Apr 15; 24(8):1504-7. PubMed ID: 8628684
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  • 56. NF1 mutation analysis using a combined heteroduplex/SSCP approach.
    Abernathy CR, Rasmussen SA, Stalker HJ, Zori R, Driscoll DJ, Williams CA, Kousseff BG, Wallace MR.
    Hum Mutat; 1997 Apr 15; 9(6):548-54. PubMed ID: 9195229
    [Abstract] [Full Text] [Related]

  • 57. 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 15; 23(5):426-36. PubMed ID: 15108273
    [Abstract] [Full Text] [Related]

  • 58. An efficient and reliable multiplex PCR-SSCP mutation analysis test applied to the human E-cadherin gene.
    Berx G, Nollet F, Strumane K, van Roy F.
    Hum Mutat; 1997 May 15; 9(6):567-74. PubMed ID: 9195232
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