Linkage analysis using heterozygote detection in phenylketonuria
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1979.tb00994.x/fullpdf
Reference25 articles.
1. A linkage study of phenylketonuria;Berg;Clin. Genet.,1974
2. Effects of oral contraceptives and obesity on carrier tests for phenylketonuria;Brown;Clin. chim. Acta,1973
3. A general model for the analysis of pedigree data;Elston;Hum. Hered.,1971
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1. Cystathionine-β-synthase deficiency: Detection of heterozygotes by the ratios of homocystein to cysteine and folate;Metabolism;1998-02
2. 6 Molecular Genetics of Phenylketonuria: From Molecular Anthropology to Gene Therapy;Advances in Genetics;1995
3. A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria;The Journal of Pediatrics;1986-10
4. Phenylketonuria (PKU) and the single gene: An old story retold;Behavior Genetics;1983-03
5. The genetic linkage between the PKU locus and the loci for Amylase1, Amylase2, Fy, PGM1, and Rh and the question of assignment of the PKU locus to chromosome No. 1;Human Genetics;1982
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