Progress in the identification of the heterozygote in phenylketonuria
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference47 articles.
1. Über Ausscheidung von Phenylbrenztraubensäure in den Harn als Stoffwechselanomalie in Verbindung mit Imbezillität;Fölling;Z Physiol Chem,1934
2. Studies on phenylpyruvic oligophrenia: the position of the metabolic error;Jervis;J Biol Chem,1947
3. The enzymatic conversion of phenylalanine to tyrosine;Udenfriend;J Biol Chem,1952
4. Phenylketonuria: epitome of human biochemical genetics. II. A review;Scriver;N Engl J Med,1980
5. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants;Guthrie;Pediatrics,1963
Cited by 14 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. Should genetic analysis in newborn screening and a heterozygote test for hyperphenylalaninaemia be recommended? An Italian study;Journal of Medical Screening;1999-12-01
4. Biochemical Phenotype and Its Relationship with Genotype in Hyperphenylalaninemia Heterozygotes;Molecular Genetics and Metabolism;1999-06
5. Discussion;Journal of Inherited Metabolic Disease;1998-08
1.学者识别学者识别
2.学术分析学术分析
3.人才评估人才评估
"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370
www.globalauthorid.com
TOP
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3