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23. Problems in screening infants for defects of amino acid metabolism. Jackson SH. Clin Biochem; 1973 Mar; 6(1):15-21. PubMed ID: 4121648 [No Abstract] [Full Text] [Related]
24. [A screening test for phenylketonuria using a paper chromatography method]. Halvorsen S, Skjelkvåle L. Lakartidningen; 1974 Mar 20; 71(12):1166-7. PubMed ID: 4821497 [No Abstract] [Full Text] [Related]
25. [Clinical and biochemical study of a case of histidinemia]. Beauvais P, Klein F, Humbel R, Dreyfus J, Gast. Arch Fr Pediatr; 1971 Feb 20; 28(2):191-203. PubMed ID: 5574024 [No Abstract] [Full Text] [Related]
26. Screening for inherited metabolic disease in Wales using urine-impregnated filter paper. Bradley DM. Arch Dis Child; 1975 Apr 20; 50(4):264-8. PubMed ID: 1147666 [Abstract] [Full Text] [Related]
30. Diagnosis and mangement of inherited aminoacidopathies in the newborn and the unborn. Rosenberg LE. Clin Endocrinol Metab; 1974 Mar 20; 3(1):145-52. PubMed ID: 4609645 [No Abstract] [Full Text] [Related]
31. [Physiological and pathological aminoacidurias]. Brodehl J. Monatsschr Kinderheilkd (1902); 1973 May 20; 121(5):190-200. PubMed ID: 4713389 [No Abstract] [Full Text] [Related]
34. Screening tests and chromatography for the detection of inborn errors of metabolism. Stuber A. Clin Chim Acta; 1972 Feb 20; 36(2):309-13. PubMed ID: 5008795 [No Abstract] [Full Text] [Related]
39. [Paper samples in detection and confirmation of some anomalies of amino acid metabolism]. Charpentier C, Lemonnier A. Ann Biol Clin (Paris); 1969 Feb 20; 27(5):297-323. PubMed ID: 4897889 [No Abstract] [Full Text] [Related]