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137 related items for PubMed ID: 2659975

  • 1. [DNA diagnosis of monogene hereditary diseases exemplified by phenylketonuria and mucoviscidosis].
    Trefz FK, Lichter-Konecki U, Krawczak M, Schmidtke J, Dueck M, Nützenadel W, Konecki DS.
    Monatsschr Kinderheilkd; 1989 Apr; 137(4):201-7. PubMed ID: 2659975
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  • 3. [Frequencies of 6 known mutations in phenylalanine hydroxylase gene and their application in prenatal gene diagnosis].
    Wang M.
    Zhonghua Yi Xue Za Zhi; 1992 Nov; 72(11):670-3, 702-3. PubMed ID: 1338705
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  • 8. Prenatal diagnosis of cystic fibrosis by chorionic villus sampling using 12 polymorphic deoxyribonucleic acid markers.
    Nugent CE, Gravius T, Green P, Larsen JW, MacMillin MD, Donis-Keller H.
    Obstet Gynecol; 1988 Feb; 71(2):213-5. PubMed ID: 3422111
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  • 9. DNA analysis of cystic fibrosis genotypes in relatives with equivocal sweat test results.
    Amos JA, Janes SR, Erbe RW.
    Clin Invest Med; 1990 Feb; 13(1):1-5. PubMed ID: 2311311
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  • 17. Molecular studies and prenatal diagnosis of phenylketonuria in Chinese patients.
    Fan GX, Qing LX, Jun Y, Mei Z.
    Southeast Asian J Trop Med Public Health; 1999 Feb; 30 Suppl 2():63-5. PubMed ID: 11400788
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  • 19. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
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  • 20. First trimester diagnosis of cystic fibrosis with linked DNA probes.
    Németi M, Papp Z.
    Acta Univ Carol Med (Praha); 1990 Mar; 36(1-4):135-8. PubMed ID: 1983382
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