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Genetic analysis of cystic fibrosis: linkage of DNA and classical markers in multiplex families.

机译:囊性纤维化的遗传分析:DNA和多重家族经典标记的联系。

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摘要

Linkage of cystic fibrosis (CF) to DNA and classical markers was studied in 36 families of two or three generations with at least two living affected children. Among the 79 affected children, no recombinants were detected between the disease and the markers MET and pJ3.11, previously shown to be linked to CF. No linkage between the human trypsin gene family (which appears to include at least 10 members) and CF was found, although not all genes of the trypsin family have been screened yet. In one of the CF families, recombination between MET and pJ3.11 was detected in an unaffected sib. Data from our families suggest that the gene order of markers among chromosome 7q is: (7cen;p8.33)collagen(COL1A2);DOCR1-917;paraoxonase+ ++(PON);(MET-cf-J3.11);T-cell receptor beta chain (TCRB);qter. There was no evidence for (or against) either postzygotic selection or meiotic drive to explain the high frequency of CF in Caucasian populations.
机译:在两个或三个世代的36个家庭中,至少有两个活着的患儿研究了囊性纤维化(CF)与DNA和经典标记的联系。在这79名患病儿童中,未在疾病与之前显示与CF相关的标记MET和pJ3.11之间检测到重组体。尽管尚未筛选出胰蛋白酶家族的所有基因,但并未发现人胰蛋白酶基因家族(似乎包含至少10个成员)与CF之间没有联系。在一个CF家族中,在未受影响的同胞中检测到MET和pJ3.11之间的重组。来自我们家庭的数据表明,7q染色体之间标记的基因顺序为:(7cen; p8.33)胶原(COL1A2); DOCR1-917;对氧磷酶+ ++(PON);(MET-cf-J3.11); T -细胞受体β链(TCRB); qter。没有证据支持(或反对)合子后选择或减数分裂驱动来解释高加索人群中CF的高发生率。

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