Newborn Screening for Urea Cycle Disorders

Author:

Naylor E. W.

Publisher

Springer US

Reference15 articles.

1. R. Guthrie and A. Susi, A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants, Pediatrics 32: 338 (1963).

2. H. Bickel, R. Guthrie, and G. Hammersen, “Neonatal Screening for Inborn Errors of Metabolism”, Springer-Verlag, Heidelberg (1980).

3. W.H. Murphey, L. Patchen, and R. Guthrie, Screening tests for argininosuccinic aciduria, orotic aciduria, and other inherited enzyme deficiencies using dried blood specimens, Biochem. Genet. 6: 51 (1972).

4. E.W. Naylor, A.P. Orfanos, and R. Guthrie, A simple screening test for arginase deficiency (hyperargininemia), J. Lab. Clin. Med. 89: 987 (1977).

5. H. Levy, P.M. Madigan, and V.E. Shih, Massachusetts metabolic disorders screening program. 1. Technics and results of urine screening, Pediatrics 49: 825 (1972).

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