Objective to identify the disease locus in X - linked retinitis pigmentosa (XLRP) families using genetic linkage analysis.
目的应用遗传连锁分析方法对X连锁型视网膜色素变性家系进行分析，确定其致病基因的所在位点。
Pedigree is one of the most general population structure in the genetic linkage analysis between human single genetic inheritance disease locus and genetic marker locus.
在人类单位点致病基因与遗传标记基因的遗传连锁分析中，家系是应用得最普遍的一种群体结构。
Genetic analysis of linkage used recombination to analyze the structure of chromosomes, to determine the locations of genes and their linear order along a chromosome.
遗传学的连锁分析是指通过遗传重组来研究染色体的结构，定位基因的位置，并确定基因在染色体上的排列顺序。
Conclusion: D12S1686 is such a valuable genetic marker that it can be used to gene linkage analysis and population genetics research.
结论D 12s1686位点具有较高的杂合度和多态信息含量，在基因连锁分析和群体遗传学研究中具有重要的应用价值。
United application of STR linkage analysis and multiplex allele specific PCR (MASPCR) in PKU genetic diagnosis was also analysed.
同时分析了STR多态性与多重等位基因特异pcr (MASPCR)在PKU基因诊断中的联合应用。
For families without inversions, it is easier and more cost-effective to undertake linkage analysis of genetic polymorphism based on PCR.
对于无倒位的家系，利用基因多态性进行遗传连锁分析较为有效可行。
For families without inversions, it is easier and more cost-effective to undertake linkage analysis of genetic polymorphism based on PCR.
对于无倒位的家系，利用基因多态性进行遗传连锁分析较为有效可行。
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