Author:
Grimm U,Knapp A,Schlenzka K,Reddemann H
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Cited by
13 articles.
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1. Phenylketonuria and Its Variants;Advances in Human Genetics;1983
2. Diagnosis of Phenylalanine Hydroxylase Deficiency (Phenylketonuria);Archives of Pediatrics & Adolescent Medicine;1982-02-01
3. The Diagnosis of Phenylketonuria;American Journal of Diseases of Children;1981-03-01
4. PHENYLKETONURIA AND OTHER PHENYLALANINE HYDROXYLATION MUTANTS IN MAN;Annual Review of Genetics;1980-12
5. REFERENCES;Acta Paediatrica;1980-04