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Journal Abstract Search

122 related items for PubMed ID: 2989834

  • 1. The human phenylalanine hydroxylase gene.
    Woo SL, Güttler F, Ledley FD, Lidsky AS, Kwok SC, DiLella AG, Robson KJ.
    Prog Clin Biol Res; 1985; 177():123-35. PubMed ID: 2989834
    [No Abstract] [Full Text] [Related]

  • 2. [Genetic diagnosis in classical phenylketonuria].
    Wulff K, Herrmann FH, Wehnert M, Seidlitz G, Schütz M.
    Z Arztl Fortbild (Jena); 1988; 82(22):1127-31. PubMed ID: 2907835
    [No Abstract] [Full Text] [Related]

  • 3. Molecular genetic analysis of phenylketonuria and mental retardation.
    Woo SL.
    Res Publ Assoc Res Nerv Ment Dis; 1991; 69():193-203. PubMed ID: 1672237
    [No Abstract] [Full Text] [Related]

  • 4. [A simple and reliable method for detection of the R408W mutation in exon 12 of the phenylalanine hydroxylase gene in the molecular diagnosis of phenylketonuria].
    Ivashchenko TE, Belova EG, Baranov VS.
    Genetika; 1993 May; 29(5):862-5. PubMed ID: 8335244
    [Abstract] [Full Text] [Related]

  • 5. [Genetic heterogeneity and approaches to the prenatal diagnosis of phenylketonuria (review)].
    Chestkov VV, Shishkin SS.
    Vopr Med Khim; 1986 May; 32(4):7-12. PubMed ID: 3020793
    [Abstract] [Full Text] [Related]

  • 6. Detection of point mutations of the phenylalanine hydroxylase gene and prenatal diagnosis of phenylketonuria.
    Fang B, Yuan L, Wang M, Huang S, Wang T, Miao S, Ye J, Sun N, Lo H, Savio LC.
    Chin Med Sci J; 1992 Dec; 7(4):205-8. PubMed ID: 1307495
    [Abstract] [Full Text] [Related]

  • 7. [Phenylketonuria].
    Oura T.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):487-92. PubMed ID: 2908394
    [No Abstract] [Full Text] [Related]

  • 8. The PKU locus in man is on chromosome 12.
    Lidksy AS, Robson KJ, Thirumalachary C, Barker PE, Ruddle FH, Woo SL.
    Am J Hum Genet; 1984 May; 36(3):527-33. PubMed ID: 6547271
    [Abstract] [Full Text] [Related]

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  • 10. Five novel missense mutations of the phenylalanine hydroxylase gene in phenylketonuria.
    Bénit P, Rey F, Melle D, Munnich A, Rey J.
    Hum Mutat; 1994 May; 4(3):229-31. PubMed ID: 7833954
    [No Abstract] [Full Text] [Related]

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  • 12. Recombinant DNA probes used to detect genetic disorders of the liver.
    Kidd VJ, Woo SL.
    Hepatology; 1984 May; 4(4):731-6. PubMed ID: 6086486
    [No Abstract] [Full Text] [Related]

  • 13. A 22-bp deletion in the phenylalanine hydroxylase gene causing phenylketonuria in an Arab family.
    Kleiman S, Schwartz G, Woo SL, Shiloh Y.
    Hum Mutat; 1992 May; 1(4):344-6. PubMed ID: 1301943
    [No Abstract] [Full Text] [Related]

  • 14. Identification and characterization of a novel liver-specific enhancer of the human phenylalanine hydroxylase gene.
    Chen KJ, Chao HK, Hsiao KJ, Su TS.
    Hum Genet; 2002 Mar; 110(3):235-43. PubMed ID: 11935335
    [Abstract] [Full Text] [Related]

  • 15. Prenatal diagnosis and carrier detection of classic phenylketonuria by gene analysis.
    Woo SL.
    Pediatrics; 1984 Sep; 74(3):412-23. PubMed ID: 6472974
    [No Abstract] [Full Text] [Related]

  • 16. DNA analysis as clinical investigation: when and how?
    Jeanpierre M, Junien C.
    Ann Genet; 1984 Sep; 27(3):134-47. PubMed ID: 6095729
    [No Abstract] [Full Text] [Related]

  • 17. [Antenatal gene diagnosis of phenylketonuria].
    Zeng YT.
    Zhonghua Yi Xue Za Zhi; 1986 Aug; 66(8):493-4. PubMed ID: 3096539
    [No Abstract] [Full Text] [Related]

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  • 20. Typing of families with classical phenylketonuria using three alleles of the Hindiii linked restriction fragment polymorphism, detectable with a phenylalanine hydroxylase cDNA probe. Family typing for PKU by linked HindIII RFLP.
    Speer A, Dahl HH, Riess O, Cobet G, Hanke R, Cotton RG, Coutelle C.
    Clin Genet; 1986 Jun; 29(6):491-5. PubMed ID: 3017615
    [Abstract] [Full Text] [Related]

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