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 *

90 related articles for article (PubMed ID: 1149276)

  • 1. Evaluation of chemical tests for heterozygosity by comparison of expected and observed numbers of heterozygotes among unaffected relatives of phenylketonurics.
    Brown ES
    Clin Chim Acta; 1975 Jul; 62(1):173-5. PubMed ID: 1149276
    [No Abstract]   [Full Text] [Related]  

  • 2. [Detection of heterozygotes in the pedigrees of phenylketonurics using variants of amylase polymorphism].
    Kamarýt J; Mrskos A; Podhradská O
    Cesk Pediatr; 1977 Aug; 32(8):449-51. PubMed ID: 597925
    [No Abstract]   [Full Text] [Related]  

  • 3. Heterozygous carriers in the relatives of a case of phenylketonuria.
    Kääriäinen R; Karlsson R
    Hereditas; 1973; 75(1):109-17. PubMed ID: 4778101
    [No Abstract]   [Full Text] [Related]  

  • 4. Unrecognized adult phenylketonuria. Implications for obstetrics and psychiatry.
    Perry TL; Hansen S; Tischler B; Richards FM; Sokol M
    N Engl J Med; 1973 Aug; 289(8):395-8. PubMed ID: 4719827
    [No Abstract]   [Full Text] [Related]  

  • 5. Phenylalanine tolerance test in parents of phenylketonurics.
    Subhash MN; Narayanan HS; Rao BS
    Acta Anthropogenet; 1980; 4(1-2):37-40. PubMed ID: 7271992
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Heterozygote detection in phenylketonuria by means of an oral load of phenylalanine].
    Dhondt JL; Farriaux JP
    J Genet Hum; 1979 Jun; 27(2):145-56. PubMed ID: 396362
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [Are heterozygotes in phenylketonuria always normal?].
    Brunecký Z; Kaláb Z; Mrskos A; Podhradská O; Veselá V
    Cesk Pediatr; 1971 Apr; 26(4):173-5. PubMed ID: 5553357
    [No Abstract]   [Full Text] [Related]  

  • 8. 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]  

  • 9. [Detection of heterozygotes of typical phenylketonuria].
    Farriaux JP; Delabre M
    Arch Fr Pediatr; 1972 Apr; 29(4):365-72. PubMed ID: 5053206
    [No Abstract]   [Full Text] [Related]  

  • 10. 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]  

  • 11. Clinical consequences of heterozygosity for autosomal-recessive diseases.
    Vogel F
    Clin Genet; 1984 May; 25(5):381-415. PubMed ID: 6373070
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 50 years ago in the Journal of Pediatrics: identification of heterozygotes with phenylketonuria on basis of blood tyrosine responses.
    Ross LF
    J Pediatr; 2012 Sep; 161(3):487. PubMed ID: 22916975
    [No Abstract]   [Full Text] [Related]  

  • 13. Genetic divergence in relatives of PKU's: low IQ correlation among normal siblings.
    Fuller RN; Shuman JB
    Dev Psychobiol; 1974 Jul; 7(4):323-30. PubMed ID: 4424629
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Contribution to the problems of determining heterozygotes in phenylketonuria by the biochemical and electroencephalographic method.
    Cechák P; Rákosníková M
    Acta Univ Carol Med Monogr; 1977; (79 Pt 3):57-64. PubMed ID: 615484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Heterozygote detection in phenylketonuria. Measurement of discriminatory ability and interpretation of the phenylalanine loading test by determination of the heterozygote likelihood ratio.
    Westwood A; Raine DN
    J Med Genet; 1975 Dec; 12(4):327-33. PubMed ID: 1219115
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. 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]  

  • 19. [Use of modified Ayling's method for detection of homozygotes and heterozygotes for phenylketonuria gene].
    Safronova EE; Rybakova NA; Annenkov GA
    Vopr Med Khim; 1982; 28(3):70-3. PubMed ID: 7101818
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Family size limitation: a method for demonstrating recessive inheritance.
    Brookfield JF; Pollitt RJ; Young ID
    J Med Genet; 1988 Mar; 25(3):181-5. PubMed ID: 3351905
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.