Galactosaemia detection as a bonus from screening for phenylketonuria

  • R. J. Pollitt
  • E. Worthy
  • A. Green
Short Communication

Keywords

Public Health Internal Medicine Metabolic Disease Phenylketonuria 

References

  1. Levy, H. L. Screening for galactosaemia (and discussion). In Burman, D., Holton, J. B. and Pennock, C. A. (eds.)Inherited Disorders of Carbohydrate Metabolism. S.S.I.E.M. Symposium 16. MTP Press, Lancaster, 1980, pp. 133–139, 157–159Google Scholar
  2. McCaman, M. W. and Robins, E. Fluorometric method for the determination of phenylalanine in serum.J. Lab. Clin. Med. 59 (1962) 885–890Google Scholar
  3. Smith, I. and Seakins, J. W. T. (eds.)Chromatographic and Electrophoretic Techniques, 4th edn, Vol. 1. Paper and Thinlayer Chromatography. Heinemann Medical, London, 1976, p. 205Google Scholar

Copyright information

© MTP Press Limited 1982

Authors and Affiliations

  • R. J. Pollitt
    • 1
  • E. Worthy
    • 2
  • A. Green
    • 2
  1. 1.Middlewood HospitalUniversity Department of Psychiatry and Trent Region Neonatal Screening LaboratorySheffield
  2. 2.Department of Chemical PathologySheffield Children's HospitalSheffield

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