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A strategy for using multiple linked markers for genetic counseling.一种使用多个连锁标记进行遗传咨询的策略。
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2
Nonrandom association of polymorphic restriction sites in the beta-globin gene cluster.β-珠蛋白基因簇中多态性限制性位点的非随机关联。
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3
Estimation of linkage disequilibrium from conditional haplotype data: application to beta-globin gene cluster in American blacks.基于条件单倍型数据的连锁不平衡估计:应用于美国黑人的β-珠蛋白基因簇
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Estimation of the marker gene frequency and linkage disequilibrium from conditional marker data.根据条件性标记数据估计标记基因频率和连锁不平衡。
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Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium.连锁标记基因在遗传咨询中的实用性和效率。III. 连锁不平衡下信息丰富家庭的比例。
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Polymorphic haplotypes and recombination rates at the LDL receptor gene locus in subjects with and without familial hypercholesterolemia who are from different populations.来自不同人群的有和没有家族性高胆固醇血症的受试者中低密度脂蛋白受体基因位点的多态性单倍型和重组率。
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5
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10
The polymorphic locus for glycogen storage disease VI (liver glycogen phosphorylase) maps to chromosome 14.
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本文引用的文献

1
The use of genetic linkage in counselling families with dystrophia myotonica.遗传连锁分析在强直性肌营养不良症家庭咨询中的应用
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Am J Hum Genet. 1982 Jul;34(4):531-51.
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Quantification of the close association between DNA haplotypes and specific beta-thalassaemia mutations in Mediterraneans.地中海人群中DNA单倍型与特定β地中海贫血突变之间紧密关联的定量分析。
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Molecular diagnostic medicine.
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Proc Natl Acad Sci U S A. 1984 Feb;81(3):853-6. doi: 10.1073/pnas.81.3.853.
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Utility and efficiency of linked marker genes for genetic counseling. III. Proportion of informative families under linkage disequilibrium.连锁标记基因在遗传咨询中的实用性和效率。III. 连锁不平衡下信息丰富家庭的比例。
Am J Hum Genet. 1983 Jul;35(4):592-610.
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Linkage disequilibrium and evolutionary relationships of DNA variants (restriction enzyme fragment length polymorphisms) at the serum albumin locus.血清白蛋白基因座处DNA变异(限制性酶切片段长度多态性)的连锁不平衡及进化关系。
Proc Natl Acad Sci U S A. 1984 Jun;81(11):3486-90. doi: 10.1073/pnas.81.11.3486.
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Am J Hum Genet. 1984 Jan;36(1):177-86.
9
Restriction fragment length polymorphisms associated with immunoglobulin C gamma genes reveal linkage disequilibrium and genomic organization.与免疫球蛋白Cγ基因相关的限制性片段长度多态性揭示了连锁不平衡和基因组组织。
Proc Natl Acad Sci U S A. 1983 Nov;80(22):6952-6. doi: 10.1073/pnas.80.22.6952.
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A polymorphic DNA marker genetically linked to Huntington's disease.一种与亨廷顿舞蹈症基因连锁的多态性DNA标记。
Nature. 1983;306(5940):234-8. doi: 10.1038/306234a0.

一种使用多个连锁标记进行遗传咨询的策略。

A strategy for using multiple linked markers for genetic counseling.

作者信息

Chakravarti A, Buetow K H

出版信息

Am J Hum Genet. 1985 Sep;37(5):984-97.

PMID:2996337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1684679/
Abstract

A strategy for using multiple linked markers for genetic counseling is to test sequentially individual markers until a diagnosis can be made. We show that in order to minimize the number of tests performed per case while diagnosing all informative cases the order in which the markers are to be tested is critical. We describe an algorithm to obtain this order using the parameter "I," the frequency of informative cases. The I value for a specific locus used depends on the marker frequency, association with the disease locus, and also on the informativeness of the marker loci already tested. Realizing that a direct assay for the beta S gene already exists, and that most cases of beta-thalassemia in Mediterraneans can be directly diagnosed using synthetic oligonucleotide probes, we illustrate the above technique by examining nine DNA polymorphisms in the human beta-globin cluster for their ability to diagnose sickle-cell anemia in American blacks and beta-thalassemia in Mediterraneans. This analysis shows that 95.39% of all sickle-cell pregnancies can be diagnosed by testing a subset of only six markers chosen by our algorithm. Furthermore, six markers can also diagnose 88.03% of beta-thalassemia in Greeks and 83.56% of beta-thalassemia in Italians. The test set is different from that suggested by the individual informative frequencies due to nonrandom associations between the restriction sites.

摘要

一种用于遗传咨询的使用多个连锁标记的策略是依次对各个标记进行检测,直到能够做出诊断。我们表明,为了在诊断所有信息性病例的同时使每个病例的检测次数最少,标记的检测顺序至关重要。我们描述了一种使用参数“I”(信息性病例的频率)来获得此顺序的算法。所使用的特定基因座的I值取决于标记频率、与疾病基因座的关联,还取决于已检测的标记基因座的信息性。鉴于已经存在针对βS基因的直接检测方法,并且地中海地区的大多数β地中海贫血病例可以使用合成寡核苷酸探针直接诊断,我们通过检查人类β珠蛋白基因簇中的九个DNA多态性来诊断美国黑人的镰状细胞贫血和地中海地区的β地中海贫血,来说明上述技术。该分析表明,通过检测我们的算法选择的仅六个标记的子集,可以诊断出所有镰状细胞妊娠的95.39%。此外,六个标记还可以诊断出希腊人β地中海贫血的88.03%和意大利人β地中海贫血的83.56%。由于限制性位点之间的非随机关联,测试集与各个信息性频率所建议的不同。