Author:
Stuhrmann M.,Riess O.,Mönch E.,Kurdoglu G.
Subject
Genetics (clinical),Genetics
Reference17 articles.
1. Apold , J. E. Odland 1988 Restriction fragmerit length polymorphisms at the phenylalan-ine hydroxylase locus in a Norwegian population Symposium on Neurogenetics, European Society of Human Genetics. Cardiff.
2. Phenylketonuria: distribution of DNA diagnostic patterns in German families;Aulehla-Scholz;Hum. Genet.,1988
3. A specific deletion within the phenylalanine hydroxylase gene is common to most Yemenite Jewish phenylketonuria patients;Avigad;Am. J. Hum. Genet.,1987
4. Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria;Chakraborty;Hum. Genet.,1987
5. Tight linkage between a splicing mutation and a specific DNA haplotype in phenylketonuria;DiLella;Nature,1986
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