Newborn Screening for Genetic Disorders
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
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2. Über Ausscheidung von Phenylbrenztraubensäure in den Harn als Stoffwecheselanomalie in Verbidung mit Imbezillitat;Fölling;Z PhysiolChem,1934
3. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963
4. Newborn screening: toward a uniform panel and system. Executive summary;Watson;Genet Med,2006
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