Author:
Gertsman Ilya,Gangoiti Jon A.,Nyhan William L.,Barshop Bruce A.
Subject
Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism
Reference46 articles.
1. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963
2. A model of human phenylalanine metabolism in normal subjects and in phenylketonuric patients;Kaufman;Proc. Natl. Acad. Sci. U. S. A.,1999
3. On the enzymic defects in hereditary tyrosinemia;Lindblad;Proc. Natl. Acad. Sci. U. S. A.,1977
4. The inclusion of succinylacetone as marker for tyrosinemia type I in expanded newborn screening programs;la Marca;Rapid Commun. Mass Spectrom.,2008
5. Richner–Hanhart syndrome and tyrosinemia type II;Hunziker;Dermatologica,1980
Cited by
38 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献