The Medical Journal of Australia · 1972 · 40 citations · 9 references
MedicineChild HealthPediatricsDevelopmental PediatricsExcretionNeonatologyAmino Acid MetabolismAmino Acid Metabolism DisordersNeonatal Metabolic DisordersNewborn Metabolic ScreeningNewborn Screening For Amino Acid Disorders
One-dimensional amino acid chromatography of urine samples from 200,000 infants usually aged between six and 12 weeks has been performed. The findings are presented and the value of the test as a screening one for phenylketonuria and other inborn errors of metabolism is discussed.
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Amino Acid Metabolism and Genetic Variation.
Annals of Internal Medicine · 1968 · 267 citations
The excretion of amino acids by cystinuric patients and their relatives
J.C. Crawhall, P. Purkiss, R. W. E. Watts et al. · Annals of Human Genetics · 1969 · 52 citations
Cystinuria: Increased Prevalence in Patients with Mental Disease
Charles R. Scriver, Donald T. Whelan, Carol L. Clow et al. · New England Journal of Medicine · 1970 · 37 citations
Life Sciences, Genetics, Psychiatry +12