The factor analytic, logarithmic and optimum solutions in separating heterozygous carriers and normal control subjects in phenylketonuria
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics,General Medicine
Reference11 articles.
1. Åmfisk program. Computing Center Univ. Jyväskylä.
2. Discriminant analysis for detection of phenylketonuric heterozygotes;Christian;Social Biol.,1971
3. Suppressor variables, prediction, and the interpretation of psychological relationships;Conger;Educ. Psychol. Meas.,1972
4. Hylps programs. Computing Center Univ. Helsinki.
5. Heterozygous carriers in the relatives of one known case of phenylketonuria;Kääriäinen;Hereditas,1973
Cited by 3 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. The role of noncoding RNAs in beta cell biology and tissue engineering;Life Sciences;2024-07
2. A method for analysing fertility of heterozygotes for autosomal recessive disorders, with special reference to cystic fibrosis, Tay-Sachs disease and phenylketonuria;Annals of Human Genetics;1977-01
3. Detection of heterozygotes for phenylketonuria and hyperphenylalaninemia by gas-chromatographic analysis of aromatic acid excretion in urine;Clinica Chimica Acta;1975-01
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