Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.-Reference-Cited by-同舟云学术

Screening for inherited metabolic disease in Wales using urine-impregnated filter paper.

Published:1975-04-01 Issue:4 Volume:50 Page:264-268
ISSN:0003-9888
Container-title:Archives of Disease in Childhood
language:en
Short-container-title:Archives of Disease in Childhood

Author:

Bradley D M

Publisher

BMJ

Subject

Pediatrics, Perinatology, and Child Health

Reference11 articles.

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2. A simple spot screening test for galactosemia;Beutler, E.; Baluda, M.C.;Journal of Laboratory and Clinical Medicine,1966

3. Influence of phenylalanine intake on phenylketonuria;Bickel, H.; Gerrard, J.; Hickmans, E.M.;Lancet,1953

4. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie, R.; Susi, A.;Pediatrics,1963

5. A thin layer chromatographic method for use in neonatal screening to detect excess amino acidaemia;Ireland, J.T.; Read, R.A.;Annals of Clinical Biochemistry,1972

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