Author:
Kozák L.,Dvořáková D.,Pijáčková A.,Kamarýt J.
Subject
Genetics (clinical),Genetics
Reference26 articles.
1. Apold J, Eiken HG, Odland, E et al (1990) A termination mutation prevalent in Norwegian haplotype 7 phenylketonuria genes.Am J Hum Genet 47: 1002–1007.
2. Aulehla-Scholz C, Vorgerd M, Sautter E et al (1988) Phenylketonuria: distribution of DNA diagnostic patterns in German families.Hum Genet 78: 353–355.
3. Berthelon M, Cailland C, Rey F et al (1991) Spectrum of phenylketonuria mutations in Western Europe and North Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locus.Hum Genet 86: 355–358.
4. Chakraborty R, Lidsky AS, Daiger SP et al (1987) Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.Hum Genet 76: 40–46.
5. Daiger SP, Chakraborty R, Reed L et al (1989) Polymorphic DNA haplotypes at the phenylalanine hydroxylase (PAH) locus in European families with phenylketonuria (PKU).Am J Hum Genet 45: 310–318.
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