Author:
Knapp A.,Tintschewa R.,Scheibe E.,J�ger B.,Biebler K. E.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference16 articles.
1. Berg K, Saugstad L (1974) A linkage study of phenylketonuria. Clin Genet 6:147?153
2. Grimm U, Knapp A, Schlenzka K, Herre R (1977) Phenylalaninhydroxylase-Aktivität bei heterozygoten Anlageträgern für das Phenylketonurie-Gen. Acta Biol Med Ger 36:1179?1182
3. Güttler F, Hansen G (1977) Different phenotypes for phenylalaninehydroxylase deficiency. Ann Clin Biochem 14:124?134
4. Kamaryt J, Laxova R (1966) Amylase heterogenety variants in man. Hum Genet 3:41?46
5. Kamaryt J, Mrskos A, Podhradska O, Kolcova V, Cabalska B, Duczynska N, Borzymowska J (1978) PKU locus: Genetic linkage with buman amylase (Amy) loci and assignment to linkage group I. Hum Genet 43:205?209