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不完全显性疾病孤立病例的正常亲属的杂合概率及其后代复发风险的计算。I. 常染色体显性基因。

Heterozygosity probabilities for normal relatives of isolated cases affected by incompletely penetrant conditions and the calculation of recurrence risks for their offspring. I. Autosomal dominant genes.

作者信息

Otto P A, Maestrelli S R

机构信息

Departamento de Biologia, Instituto de Biociências, Universidade de São Paulo, São Paulo, Brazil.

出版信息

Am J Med Genet. 2000 Nov 6;95(1):43-8.

Abstract

Heterozygosity probabilities P(het) for relatives of isolated cases produced by incompletely penetrant autosomal dominant genes and recurrence risks for their offspring, R = P(het).K/2, where K is the penetrance value, have been calculated in the literature for some simple particular situations. Bayes theorem and elements from the theory of finite difference equations enabled us to derive the heterozygosity probability for any individual belonging to a pedigree containing an isolated case affected with an incompletely penetrant autosomal dominant disorder. The generalized formula here derived is valid for most particular cases thus far studied in the literature.

摘要

对于由不完全显性常染色体显性基因产生的散发病例亲属的杂合概率P(het)以及其后代的复发风险R = P(het).K/2(其中K是外显率值),在文献中已针对一些简单的特定情况进行了计算。贝叶斯定理和有限差分方程理论的要素使我们能够推导出属于包含患有不完全显性常染色体显性疾病散发病例的家系中任何个体的杂合概率。这里推导的广义公式对文献中迄今研究的大多数特定情况均有效。

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