Author:
Lichter-Konecki Uta,Schlotter Magdalena,Konecki David S.,Labeit Sigfried,Woo Savio L. C.,Trefz Friedrich K.
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Reference27 articles.
1. Bartholomé K, Lutz P, Bickel H (1975) Determination of phenylalanine hydroxylase activity in patients with phenylketonuria and hyperphenylalaninemia. Pediatr Res 9:899?903
2. Blaskovics M, Schaeffer G, Hack S (1974) Phenylalaninemia: differetial diagnosis. Arch Dis Child 49:835?843
3. Chakraborty R, Lidsky AS, Daiger SP, Güttler F, Sullivan S, DiLella AG, Woo SLC (1987) Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria. Hum Genet 76:40?46
4. Chakravarti A, Phillips III JA, Mellits KH, Buetow KH, Seeburg PH (1984) Patterns of polymorphism and linkage disequilibrium suggest independent origins of the human growth hormone gene cluster. Proc Natl Acad Sci USA 81:6085?6089
5. Daiger SP, Lidsky AS, Chakraborty R, Koch R, Güttler F, Woo SLC (1986) Polymorphic DNA haplotypes at the phenylalanine hydroxylase locus in prenatal diagnosis of phenylketonuria. Lancet I:299?232
Cited by
28 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