A simplified test to detect PKU heterozygotes by discriminant analysis in mentally retarded children and their mothers
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb03444.x/fullpdf
Reference16 articles.
1. Phenylalanine loading and aromatic acid excretion in normal subjects and heterozygotes for phenylketonuria;Blau;Clin. Chim. Acta,1973
2. Carrier screening for phenylketonuria: comparison of two discriminant analysis procedures;Freehauf;Am. J. Hum. Genet.,1984
3. Relative inability of mother and child to convert phenylalanine to tyrosine. A possible cause of non-specific mental retardation;Fujmoto;Biochem. Med.,1979
4. Classic phenylketonuria: diagnosis through heterozygotes detection;Griffin;J. Pediatr.,1975
5. Heterozygote detection in phenylketonuria;Güttler;Clin. Genet.,1977
Cited by 4 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
1. Phenylalanine and Tyrosine Metabolism Analysis in Heterozygotes for Phenylketonuria and in Healthy Individuals;Journal of Inborn Errors of Metabolism and Screening;2015-02-18
2. Evaluation of an aspartame loading test for the detection of heterozygotes for classical phenylketonuria;Clinical Genetics;2008-06-28
3. Inherited metabolic diseases affecting the carrier;Journal of Inherited Metabolic Disease;1997-03
4. Heterozygous carriers of classical phenylketonuria in a sample of the turkish population: Detection by a spectrofluorimetric method;Journal of Inherited Metabolic Disease;1991-09
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