A study of the cause of the high incidence of phenylketonuria in Ireland and west Scotland.
作者信息
Woolf L I
出版信息
Ir Med J. 1976 Sep 30;69(15):398-401.
PMID:1010729
Abstract
摘要
相似文献
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A study of the cause of the high incidence of phenylketonuria in Ireland and west Scotland.
Ir Med J. 1976 Sep 30;69(15):398-401.
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Why are some genetic diseases common? Distinguishing selection from other processes by molecular analysis of globin gene variants.为什么有些遗传疾病很常见？通过对珠蛋白基因变异进行分子分析来区分选择与其他过程。
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3
The heterozygote advantage in phenylketonuria.苯丙酮尿症的杂合子优势
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Polymorphic DNA haplotypes at the human phenylalanine hydroxylase locus and their relationship with phenylketonuria.人类苯丙氨酸羟化酶基因座的多态性DNA单倍型及其与苯丙酮尿症的关系。
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Molecular genetics of phenylketonuria and its implications.苯丙酮尿症的分子遗传学及其影响
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The phenylketonuria locus: current knowledge about alleles and mutations of the phenylalanine hydroxylase gene in various populations.苯丙酮尿症基因座：不同人群中苯丙氨酸羟化酶基因的等位基因和突变的现有知识。
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The high frequency of phenylketonuria in Ireland and Western Scotland.
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