Dawson E, Powell J F, Sham P, Shaikh S, Taylor C, Clements A, Asherson P, Sargeant M, Collier D, Nanko S
Department of Neuroscience, Institute of Psychiatry, De Crespigny Park, London.
Am J Med Genet. 1995 Oct 9;60(5):424-33. doi: 10.1002/ajmg.1320600513.
We describe a method of systematically searching for major genes in disorders of unknown mode of inheritance, using linkage analysis. Our method is designed to minimize the probability of missing linkage due to inadequate exploration of data. We illustrate this method with the results of a search for a locus for schizophrenia on chromosome 12 using 22 highly polymorphic markers in 23 high density pedigrees. The markers span approximately 85-90% of the chromosome and are on average 9.35 cM apart. We have analysed the data using the most plausible current genetic models and allowing for the presence of genetic heterogeneity. None of the markers was supportive of linkage and the distribution of the heterogeneity statistics was in accordance with the null hypothesis.
我们描述了一种使用连锁分析系统搜索未知遗传模式疾病中主要基因的方法。我们的方法旨在将因数据探索不足而遗漏连锁的可能性降至最低。我们用在23个高密度家系中使用22个高度多态性标记对12号染色体上精神分裂症位点进行搜索的结果来说明这种方法。这些标记覆盖了该染色体约85 - 90%的区域,平均间距为9.35厘摩。我们使用当前最合理的遗传模型分析了数据,并考虑了遗传异质性的存在。没有一个标记支持连锁,异质性统计量的分布符合无效假设。