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Clinical Specialties & Practice › GENETICS / HEREDITY › HEREDITARY / CONGENITAL DISEASES OR DISORDERS › Inherited Metabolic Disorders › Phenylketonuria
Phenylketonuria
Exhibiting 1 entries found in the GMN corpus.
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1963 CE
A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants.
Pediatrics
Genetics & Heredity
Women & Gender
GUTHRIE, Robert (1916 – 1995)
SUSI, Ada J. (1918 – 2002)
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