These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

156 related articles for article (PubMed ID: 2563988)

  • 1. Study of restriction fragment length polymorphisms at the human phenylalanine hydroxylase locus and evaluation of its potential application in prenatal diagnosis of phenylketonuria in Chinese.
    Chen SH; Hsiao KJ; Lin LH; Liu TT; Tang RB; Su TS
    Hum Genet; 1989 Feb; 81(3):226-30. PubMed ID: 2563988
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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; 1(8475):229-32. PubMed ID: 2868252
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuria.
    Lidsky AS; Ledley FD; DiLella AG; Kwok SC; Daiger SP; Robson KJ; Woo SL
    Am J Hum Genet; 1985 Jul; 37(4):619-34. PubMed ID: 9556654
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Analysis of short tandem repeats polymorphism in the phenylalanine hydroxylase gene and its application to prenatal gene diagnosis of phenylketonuria].
    Huang S; Fang B; Chu H
    Zhonghua Yi Xue Za Zhi; 1995 Jan; 75(1):22-4, 61. PubMed ID: 7600314
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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; 45(2):319-24. PubMed ID: 2569272
    [TBL] [Abstract][Full Text] [Related]  

  • 6. RFLPs of the phenylalanine hydroxylase gene in the Italian population.
    Dianzani I; Farinasso L; Fortina P; Camaschella C; Ponzone R; Dahl HH; Cotton RG; Ponzone A
    J Inherit Metab Dis; 1989; 12(2):162-5. PubMed ID: 2569049
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A study on Chinese phenylalanine hydroxylase gene restriction site polymorphism.
    Zeng YT; Huang SZ; Chen MJ; Zhang ML; Ren ZR; Xu YH; Peng SF; Woo SL
    Sci Sin B; 1988 Dec; 31(12):1447-53. PubMed ID: 2908213
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A single polymorphic STR system in the human phenylalanine hydroxylase gene permits rapid prenatal diagnosis and carrier screening for phenylketonuria.
    Goltsov AA; Eisensmith RC; Naughton ER; Jin L; Chakraborty R; Woo SL
    Hum Mol Genet; 1993 May; 2(5):577-81. PubMed ID: 8100164
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus and their relation to phenotype in Swedish phenylketonuria families.
    Svensson E; von Döbeln U; Hagenfeldt L
    Hum Genet; 1991 May; 87(1):11-7. PubMed ID: 1674714
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 110(1):68-71. PubMed ID: 2878985
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Cloned human phenylalanine hydroxylase gene allows prenatal diagnosis and carrier detection of classical phenylketonuria.
    Woo SL; Lidsky AS; Güttler F; Chandra T; Robson KJ
    Nature; 1983 Nov 10-16; 306(5939):151-5. PubMed ID: 6316140
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Modern techniques of differentiating the various phenotypes of phenylketonuria.
    Guttler F
    Postgrad Med J; 1989; 65 Suppl 2():S2-6. PubMed ID: 2576129
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A simple, rapid, and highly informative PCR-based procedure for prenatal diagnosis and carrier screening of phenylketonuria.
    Eisensmith RC; Goltsov AA; Woo SL
    Prenat Diagn; 1994 Dec; 14(12):1113-8. PubMed ID: 7899279
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of RFLP haplotypes and point mutations at the phenylalanine hydroxylase (PAH) locus in PKU families from north China].
    Fang B
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1992 Feb; 14(1):46-50. PubMed ID: 1350519
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 16(2):451-6. PubMed ID: 8105144
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Haplotype analysis of the phenylalanine hydroxylase gene in Turkish phenylketonuria families.
    Stuhrmann M; Riess O; Mönch E; Kurdoglu G
    Clin Genet; 1989 Aug; 36(2):117-21. PubMed ID: 2569949
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.
    Chakraborty R; Lidsky AS; Daiger SP; Güttler F; Sullivan S; Dilella AG; Woo SL
    Hum Genet; 1987 May; 76(1):40-6. PubMed ID: 2883110
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.