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 *

75 related articles for article (PubMed ID: 568666)

  • 1. Heterozygote advantage for the phenylketonuria allele.
    Saugstad LF
    J Med Genet; 1978 Aug; 15(4):317-9. PubMed ID: 568666
    [No Abstract]   [Full Text] [Related]  

  • 2. Heterozygote advantage for the phenylketonuria allele.
    Smith I; Carter CO; Wolff OH
    J Med Genet; 1978 Jun; 15(3):246-8. PubMed ID: 671494
    [No Abstract]   [Full Text] [Related]  

  • 3. Anthropological significance of phenylketonuria and the importance of heterozygote advantage.
    Saugstad LF
    Ir Med J; 1976 Sep; 69(15):405-10. PubMed ID: 1010731
    [No Abstract]   [Full Text] [Related]  

  • 4. Phenylketonuria as a balanced polymorphism: the nature of the heterozygote advantage.
    Woolf LI; McBean MS; Woolf FM; Cahalane SF
    Ann Hum Genet; 1975 May; 38(4):461-9. PubMed ID: 1190737
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Anthropological significance of phenylketonuria.
    Saugstad LF
    Clin Genet; 1975 Jan; 7(1):52-61. PubMed ID: 803884
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Heterozygote advantage for the phenylketonuria allele.
    Saugstad LF
    J Med Genet; 1977 Feb; 14(1):20-4. PubMed ID: 839495
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria.
    KNOX WE; MESSINGER EC
    Am J Hum Genet; 1958 Mar; 10(1):53-60. PubMed ID: 13520699
    [No Abstract]   [Full Text] [Related]  

  • 8. Factors determining the birth frequency of recessive conditions-a high frequency of classical phenylketonuria in Ireland.
    Carter CO
    Ir Med J; 1976 Sep; 69(15):386-9. PubMed ID: 1010724
    [No Abstract]   [Full Text] [Related]  

  • 9. Birthweight of infants with phenylketonuria and their unaffected siblings.
    Smith I; Carter CO; Wolfe OH
    J Inherit Metab Dis; 1978; 1(3):99-100. PubMed ID: 116086
    [No Abstract]   [Full Text] [Related]  

  • 10. A study of the cause of the high incidence of phenylketonuria in Ireland and west Scotland.
    Woolf LI
    Ir Med J; 1976 Sep; 69(15):398-401. PubMed ID: 1010729
    [No Abstract]   [Full Text] [Related]  

  • 11. [Intravenous loading of L-phenylalanine: detection of heterozygotes in phenylketonuria].
    Lambert J; Viailhet M; Monot C; Lepoire E; Baradel J; Nabet P; Martin J; Pierson M
    C R Seances Soc Biol Fil; 1973; 167(3):502-8. PubMed ID: 4785089
    [No Abstract]   [Full Text] [Related]  

  • 12. The high frequency of phenylketonuria in Ireland and Western Scotland.
    Woolf LI
    J Inherit Metab Dis; 1978; 1(3):101-3. PubMed ID: 116076
    [No Abstract]   [Full Text] [Related]  

  • 13. The occurrence of phenylketonuria and galactosemia within the same family.
    Fisch RO; Goosens KA; Tsai MY; Seelig S; Schwichtenberg K
    Clin Pediatr (Phila); 1985 Aug; 24(8):456-8. PubMed ID: 4006356
    [No Abstract]   [Full Text] [Related]  

  • 14. Increased "reproductive casualty" in heterozygotes for phenylketonuria.
    Saugstad LF
    Clin Genet; 1973; 4(2):105-14. PubMed ID: 4730939
    [No Abstract]   [Full Text] [Related]  

  • 15. Birth weight and pathogenesis in phenylketonuria.
    Crockett DJ; Woolf LI; McBean MS; Woolf FM; Cahalane SF
    Int J Neurosci; 1990 Oct; 54(3-4):259-66. PubMed ID: 2265974
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The heterozygote advantage in phenylketonuria.
    Woolf LI
    Am J Hum Genet; 1986 May; 38(5):773-5. PubMed ID: 3717163
    [No Abstract]   [Full Text] [Related]  

  • 17. Inbreeding and PKU allele frequency: Estimating by microsatellite approaches.
    Santos LL; da Fonseca CG; Vaintraub MT; Vaintraub P; Januário JN; de Aguiar MJ; Raquel Santos Carvalho M
    Am J Hum Biol; 2010; 22(5):716-9. PubMed ID: 20737622
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Phenylketonuria: mental illness in heterozygotes.
    Larson CA; Nyman GE
    Psychiatr Clin (Basel); 1968; 1(6):367-74. PubMed ID: 5715864
    [No Abstract]   [Full Text] [Related]  

  • 19. Phenylketonuria (PKU) and the single gene: an old story retold.
    Murphey RM
    Behav Genet; 1983 Mar; 13(2):141-57. PubMed ID: 6860251
    [No Abstract]   [Full Text] [Related]  

  • 20. Phenylketonuria mutations in Europe.
    Zschocke J
    Hum Mutat; 2003 Apr; 21(4):345-56. PubMed ID: 12655544
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.