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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

98 related items for PubMed ID: 8809899

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  • 6. Prenatal exclusion testing for Huntington disease using the polymerase chain reaction.
    McIntosh I, Curtis A, Millan FA, Brock DJ.
    Am J Med Genet; 1989 Feb; 32(2):274-6. PubMed ID: 2564738
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  • 7. Accurate prenatal diagnosis of Hb Bart's hydrops fetalis in daily practice with a double-check PCR system.
    Karnpean R, Fucharoen G, Fucharoen S, Sae-ung N, Sanchaisuriya K, Ratanasiri T.
    Acta Haematol; 2009 Feb; 121(4):227-33. PubMed ID: 19546525
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  • 8. DNA-based prenatal diagnosis of heritable skin diseases.
    Christiano AM, Uitto J.
    Arch Dermatol; 1993 Nov; 129(11):1455-9. PubMed ID: 7902070
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  • 13. Molecular exclusion of haemoglobin SD disease by prenatal diagnosis.
    Fodor FH, Eng CM.
    Prenat Diagn; 1999 Jan; 19(1):58-60. PubMed ID: 10073909
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  • 15. Use of polymerase chain reaction single-strand conformation polymorphism (PCR-SSCP) analysis to detect a point mutation in the catalase-peroxidase gene (katG) of Mycobacterium tuberculosis.
    Temesgen Z, Satoh K, Uhl JR, Kline BC, Cockerill FR.
    Mol Cell Probes; 1997 Feb; 11(1):59-63. PubMed ID: 9076716
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  • 18. Infantile hypophosphatasia: successful prenatal assessment by testing for tissue-non-specific alkaline phosphatase isoenzyme gene mutations.
    Henthorn PS, Whyte MP.
    Prenat Diagn; 1995 Nov; 15(11):1001-6. PubMed ID: 8606878
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