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Journal Abstract Search

276 related items for PubMed ID: 1674714

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  • 3. Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria.
    Daiger SP, Lidsky AS, Chakraborty R, Koch R, Güttler F, Woo SL.
    Lancet; 1986 Feb 01; 1(8475):229-32. PubMed ID: 2868252
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  • 4. Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in Asian families with phenylketonuria (PKU).
    Daiger SP, Reed L, Huang SS, Zeng YT, Wang T, Lo WH, Okano Y, Hase Y, Fukuda Y, Oura T.
    Am J Hum Genet; 1989 Aug 01; 45(2):319-24. PubMed ID: 2569272
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  • 5. Correlation between polymorphic DNA haplotypes at phenylalanine hydroxylase locus and clinical phenotypes of phenylketonuria.
    Güttler F, Ledley FD, Lidsky AS, DiLella AG, Sullivan SE, Woo SL.
    J Pediatr; 1987 Jan 01; 110(1):68-71. PubMed ID: 2878985
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  • 6. Relation between genotype and phenotype in Swedish phenylketonuria and hyperphenylalaninemia patients.
    Svensson E, von Döbeln U, Eisensmith RC, Hagenfeldt L, Woo SL.
    Eur J Pediatr; 1993 Feb 01; 152(2):132-9. PubMed ID: 8444221
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  • 7. An amino-acid substitution involved in phenylketonuria is in linkage disequilibrium with DNA haplotype 2.
    DiLella AG, Marvit J, Brayton K, Woo SL.
    Nature; 1993 Feb 01; 327(6120):333-6. PubMed ID: 2884570
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  • 9. Modern techniques of differentiating the various phenotypes of phenylketonuria.
    Guttler F.
    Postgrad Med J; 1989 Feb 01; 65 Suppl 2():S2-6. PubMed ID: 2576129
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  • 12. Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus.
    Berthelon M, Caillaud C, Rey F, Labrune P, Melle D, Feingold J, Frézal J, Briard ML, Farriaux JP, Guibaud P.
    Hum Genet; 1991 Feb 01; 86(4):355-8. PubMed ID: 1671847
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  • 13. Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU).
    Daiger SP, Chakraborty R, Reed L, Fekete G, Schuler D, Berenssi G, Nasz I, Brdicka R, Kamarýt J, Pijácková A.
    Am J Hum Genet; 1989 Aug 01; 45(2):310-8. PubMed ID: 2569271
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  • 15. Haplotype distribution at the phenylalanine hydroxylase locus in PKU families from the Moravian area of Czechoslovakia.
    Kozák L, Dvoráková D, Pijácková A, Kamarýt J.
    J Inherit Metab Dis; 1993 Aug 01; 16(2):451-6. PubMed ID: 8105144
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  • 17. Haplotype distribution of the human phenylalanine hydroxylase locus in Scotland and Switzerland.
    Sullivan SE, Moore SD, Connor JM, King M, Cockburn F, Steinmann B, Gitzelmann R, Daiger SP, Woo SL.
    Am J Hum Genet; 1989 May 01; 44(5):652-9. PubMed ID: 2565077
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  • 19. RFLP haplotyping and mutation analysis of the phenylalanine hydroxylase gene in Dutch phenylketonuria families.
    Meijer H, Jongbloed RJ, Hekking M, Spaapen LJ, Geraedts JP.
    Hum Genet; 1993 Dec 01; 92(6):588-92. PubMed ID: 7903270
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