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Logo of procrsmedFormerly medchtJournal of the Royal Society of MedicineProceedings of the Royal Society of Medicine
 
Proc R Soc Med. 1968 August; 61(8): 766–767.
PMCID: PMC1902463

Paediatric screening for genetically determined metabolic diseases.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • EFRON ML, YOUNG D, MOSER HW, MACCREADY RA. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER. N Engl J Med. 1964 Jun 25;270:1378–1383. [PubMed]
  • GIBBS NK, WOOLF LI. Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives. Br Med J. 1959 Sep 26;2(5151):532–535. [PMC free article] [PubMed]
  • HILL JB, SUMMER GK, PENDER MW, ROSZEL NO. AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE. Clin Chem. 1965 May;11:541–546. [PubMed]
  • SCRIVER CR, DAVIES E, CULLEN AM. APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIES. Lancet. 1964 Aug 1;2(7353):230–232. [PubMed]
  • Searle B, Mijuskovic MB, Widelock D, Davidow B. A manual fluorometric paper disc method for detecting phenylketonuria. Clin Chem. 1967 Aug;13(8):621–625. [PubMed]
  • Stephenson JB, McBean MS. Phenylketonuria: a reassessment of mass infant screening by napkin test. Br Med J. 1967 Sep 2;3(5565):582–582. [PMC free article] [PubMed]

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