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苯丙酮尿症的携带者筛查:两种判别分析程序的比较。

Carrier screening for phenylketonuria: comparison of two discriminant analysis procedures.

作者信息

Freehauf C L, Lezotte D, Goodman S I, McCabe E R

出版信息

Am J Hum Genet. 1984 Nov;36(6):1180-9.

Abstract

Absence of a convenient, direct enzyme assay for detecting phenylketonuria (PKU) heterozygotes has resulted in continued effort to develop an accurate and reliable procedure to discriminate the heterozygous individual from the homozygous normal. Our study compares two statistical procedures that combine the semifasting plasma phenylalanine and tyrosine concentrations with the individuals' prior probability of being a heterozygous carrier in order to discriminate carriers from noncarriers. The results of this comparison indicate that the quadratic discriminant function is superior to the linear discriminant function as a method of carrier testing both in theory and in practice. An interactive computer system is described that facilitates the clinical utilization of the quadratic discriminant function.

摘要

由于缺乏一种方便、直接的酶检测方法来检测苯丙酮尿症(PKU)杂合子,人们一直在努力开发一种准确可靠的程序,以区分杂合子个体与纯合正常个体。我们的研究比较了两种统计程序,它们将半空腹血浆苯丙氨酸和酪氨酸浓度与个体作为杂合子携带者的先验概率相结合,以区分携带者和非携带者。比较结果表明,二次判别函数在理论和实践上作为一种携带者检测方法都优于线性判别函数。本文描述了一种交互式计算机系统,它有助于二次判别函数在临床上的应用。

相似文献

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A simple method for detection of heterozygous carriers of the gene for classic phenylketonuria.
J Pediatr. 1986 Oct;109(4):601-4. doi: 10.1016/s0022-3476(86)80220-7.
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Heterozygote detection in phenylketonuria.苯丙酮尿症杂合子检测
Clin Genet. 1977 Feb;11(2):137-46. doi: 10.1111/j.1399-0004.1977.tb01291.x.

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