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Journal Abstract Search

117 related items for PubMed ID: 2239966

  • 1. Rapid detection of the hemoglobin C mutation by allele-specific polymerase chain reaction.
    Fischel-Ghodsian N, Hirsch PC, Bohlman MC.
    Am J Hum Genet; 1990 Dec; 47(6):1023-4. PubMed ID: 2239966
    [No Abstract] [Full Text] [Related]

  • 2. Phenylketonuria: detection of a frequent haplotype 4 allele mutation.
    Dworniczak B, Aulehla-Scholz C, Horst J.
    Hum Genet; 1989 Dec; 84(1):95-6. PubMed ID: 2606484
    [Abstract] [Full Text] [Related]

  • 3. Molecular characterization of hemoglobin C in Thailand.
    Sanchaisuriya K, Fucharoen G, Sae-ung N, Siriratmanawong N, Surapot S, Fucharoen S.
    Am J Hematol; 2001 Jul; 67(3):189-93. PubMed ID: 11391717
    [Abstract] [Full Text] [Related]

  • 4. A novel transthyretin mutation associated with familial amyloidotic polyneuropathy.
    Murakami T, Maeda S, Yi S, Ikegawa S, Kawashima E, Onodera S, Shimada K, Araki S.
    Biochem Biophys Res Commun; 1992 Jan 31; 182(2):520-6. PubMed ID: 1734866
    [Abstract] [Full Text] [Related]

  • 5. Optimisation and properties of a UHG for genotyping of hemoglobins S and C.
    Wood N, Standen G, Old J, Bidwell J.
    Hum Mutat; 1995 Jan 31; 5(2):166-72. PubMed ID: 7749414
    [Abstract] [Full Text] [Related]

  • 6. Rapid detection of hemoglobin variants by mutagenically separated polymerase chain reaction (MS-PCR).
    Chang JG, Chang CP, Lu CM, Huang JM, Chen JT, Liu HJ.
    Ann Hematol; 1995 Aug 31; 71(2):97-100. PubMed ID: 7654858
    [Abstract] [Full Text] [Related]

  • 7. Incidence of Hb C trait in an area of southern Spain.
    de Pablos JM.
    Br J Haematol; 1985 Jul 31; 60(3):584-5. PubMed ID: 4015993
    [No Abstract] [Full Text] [Related]

  • 8. Non-enzymatic digoxigenin labeling of allele-specific oligonucleotides for the detection of the sickle cell mutation.
    Bürgi W, Keller E, Schmidheini T.
    Eur J Haematol; 1992 Nov 31; 49(5):275-6. PubMed ID: 1473589
    [No Abstract] [Full Text] [Related]

  • 9. Priapism associated with hemoglobin C trait.
    Gibson BR, Peterson AC, Costabile RA.
    J Urol; 2002 Nov 31; 168(5):2122. PubMed ID: 12394727
    [No Abstract] [Full Text] [Related]

  • 10. Detection of allele-specific transcripts by the polymerase chain reaction (AST-PCR).
    Top B, van den Boorn N, van der Zee A, Havekes LM, Frants RR.
    Biochem Biophys Res Commun; 1991 Aug 15; 178(3):1319-25. PubMed ID: 1714719
    [Abstract] [Full Text] [Related]

  • 11. Rapid detection of Chinese G gamma+(A gamma delta beta)zero-thalassemia by polymerase chain reaction.
    Ko TM, Tseng LH, Hsieh FJ, Chuang SM, Lee TY.
    Acta Haematol; 1993 Aug 15; 89(2):80-1. PubMed ID: 8503248
    [Abstract] [Full Text] [Related]

  • 12. ShiftDetector: detection of shift mutations.
    Seroussi E, Ron M, Kedra D.
    Bioinformatics; 2002 Aug 15; 18(8):1137-8. PubMed ID: 12176839
    [Abstract] [Full Text] [Related]

  • 13. Single nucleotide primer extension to detect genetic diseases: experimental application to hemophilia B (factor IX) and cystic fibrosis genes.
    Kuppuswamy MN, Hoffmann JW, Kasper CK, Spitzer SG, Groce SL, Bajaj SP.
    Proc Natl Acad Sci U S A; 1991 Feb 15; 88(4):1143-7. PubMed ID: 1671714
    [Abstract] [Full Text] [Related]

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  • 18. Rapid diagnostic test for hereditary nonpolyposis colon cancer kindred using polymerase chain reaction.
    Faragher IG, Whitehead RH.
    Dis Colon Rectum; 1998 Jul 15; 41(7):938-40. PubMed ID: 9678385
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  • 20. Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser-induced capillary fluorescence detection.
    Day NS, Tadin M, Christiano AM, Lanzano P, Piomelli S, Brown S.
    Prenat Diagn; 2002 Aug 15; 22(8):686-91. PubMed ID: 12210577
    [Abstract] [Full Text] [Related]

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