Skip to main content
American Journal of Human Genetics logoLink to American Journal of Human Genetics
. 1961 Jun;13(2):255–261.

Increased Reliability for the Determination of the Carrier State in Phenylketonuria

Reviewed by: Hwa L Wang, N E Morton, Harry A Waisman
PMCID: PMC1932125  PMID: 13783038

Full text

PDF
259

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. DRISCOLL K. W., HSIA D. Y., KNOX W. E., TROLL W. Detection by phenylalanine tolerance tests of heterozygous carriers of phenylketonuria. Nature. 1956 Dec 1;178(4544):1239–1240. doi: 10.1038/1781239a0. [DOI] [PubMed] [Google Scholar]
  2. HSIA D. Y., STEINBERG A. G. Studies on linkage between phenylketonuria and the blood groups. Am J Hum Genet. 1960 Sep;12:277–286. [PMC free article] [PubMed] [Google Scholar]
  3. KNOX W. E., MESSINGER E. C. The detection in the heterozygote of the metabolic effect of the recessive gene for phenylketonuria. Am J Hum Genet. 1958 Mar;10(1):53–60. [PMC free article] [PubMed] [Google Scholar]
  4. PENROSE L. S. Measurement of pleiotropic effects in phenylketonuria. Ann Eugen. 1951 Sep;16(2):134–141. doi: 10.1111/j.1469-1809.1951.tb02467.x. [DOI] [PubMed] [Google Scholar]
  5. RENWICK J. H., LAWLER S. D., COWIE V. A. Phenylketonuria: a linkage study using phenylalanine tolerance tests. Am J Hum Genet. 1960 Sep;12:287–322. [PMC free article] [PubMed] [Google Scholar]
  6. UDENFRIEND S., COOPER J. R. Assay of L-phenylalanine as phenylethylamine after enzymatic decarboxylation; application to isotopic studies. J Biol Chem. 1953 Aug;203(2):953–960. [PubMed] [Google Scholar]
  7. UDENFRIEND S., COOPER J. R. The chemical estimation of tyrosine and tyramine. J Biol Chem. 1952 May;196(1):227–233. [PubMed] [Google Scholar]

Articles from American Journal of Human Genetics are provided here courtesy of American Society of Human Genetics

RESOURCES