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1
The number of families required to detect or exclude linkage heterogeneity.检测或排除连锁异质性所需的家系数量。
Am J Hum Genet. 1986 Aug;39(2):159-65.
2
The detection of linkage and heterogeneity in nuclear families for complex disorders: one versus two marker loci.复杂疾病核心家系中连锁与遗传异质性的检测:单标记位点与双标记位点比较
Am J Hum Genet. 1989 Apr;44(4):552-9.
3
A combined test of linkage heterogeneity.连锁异质性的联合检验。
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4
Genetic linkage between a locus for 6-PGD and the Rh locus: evaluation of possible heterogeneity in the recombination fraction between sexes and among families.6 -磷酸葡萄糖脱氢酶(6 - PGD)基因座与Rh基因座之间的遗传连锁:两性间及家系间重组率可能存在的异质性评估。
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5
Power to detect linkage with heterogeneity in samples of small nuclear families.在小型核心家庭样本中检测连锁与异质性的效能。
Am J Med Genet. 1993 Jul 15;48(2):94-102. doi: 10.1002/ajmg.1320480208.
6
Estimating the power of a proposed linkage study for a complex genetic trait.估计针对复杂遗传性状的拟连锁研究的效能。
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Risk calculations under heterogeneity.异质性下的风险计算
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Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies.人类家系中重组率的估计:人类连锁研究似然性的高效计算。
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Comparison of sequential and fixed-structure sampling of pedigrees in complex segregation analysis of a quantitative trait.复杂数量性状分离分析中系谱的序贯抽样与固定结构抽样的比较
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Genetic heterogeneity of X-linked mental retardation with fragile X. Association of tight linkage to factor IX and incomplete penetrance in males.伴有脆性X的X连锁智力迟钝的遗传异质性。与凝血因子IX紧密连锁及男性不完全外显率的关联。
Ann Hum Genet. 1987 May;51(2):107-24. doi: 10.1111/j.1469-1809.1987.tb01052.x.

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Follow-up examination of linkage and association to chromosome 1q43 in multiple sclerosis.多发性硬化症中与1号染色体1q43的连锁和关联的随访检查。
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A second-generation genomic screen for multiple sclerosis.针对多发性硬化症的第二代基因组筛查。
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Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.骨佩吉特病:5q35 - qter和5q31两个基因座的定位
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6
The detection of linkage and heterogeneity in nuclear families for complex disorders: one versus two marker loci.复杂疾病核心家系中连锁与遗传异质性的检测:单标记位点与双标记位点比较
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Prenatal prediction of osteogenesis imperfecta (OI type IV): exclusion of inheritance using a collagen gene probe.成骨不全(IV型)的产前预测:使用胶原蛋白基因探针排除遗传因素
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8
Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci.X连锁无丙种球蛋白血症与九个限制性片段长度多态性(RFLP)位点图谱之间的图谱距离的异质性。
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9
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2.显性遗传的成骨不全症与I型胶原基因座COL1A1和COL1A2的一致连锁关系。
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10
Sampling strategies for linkage studies.
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本文引用的文献

1
Detection of inbreeding effects by the chi-square test on genotypic and phenotypic frequencies.通过对基因型和表型频率进行卡方检验来检测近亲繁殖效应。
Am J Hum Genet. 1980 Sep;32(5):754-60.
2
Detecting linkage for genetically heterogeneous diseases and detecting heterogeneity with linkage data.检测基因异质性疾病的连锁关系以及利用连锁数据检测异质性。
Am J Hum Genet. 1986 May;38(5):599-616.

检测或排除连锁异质性所需的家系数量。

The number of families required to detect or exclude linkage heterogeneity.

作者信息

Ott J

出版信息

Am J Hum Genet. 1986 Aug;39(2):159-65.

PMID:3752084
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1683933/
Abstract

Under the assumption of two family types, one with linkage and one without linkage, the number of phase-known double-backcross families required to detect heterogeneity is investigated. The case of testing for heterogeneity with two offspring per family is shown to be formally equivalent to testing for inbreeding effects in a sample of unrelated individuals.

摘要

在假设有两种家系类型(一种存在连锁,一种不存在连锁)的情况下,研究了检测异质性所需的已知相双回交家系的数量。结果表明,每个家系有两个后代时检测异质性的情况在形式上等同于在无关个体样本中检测近亲繁殖效应。