以下为句子列表：
英文: Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: An ERP study
中文: Prader-Willi综合征亲源染色体缺失和母源单亲二体染色体之间行为表型的差异:一项事件相关脑活动(ERP)研究
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英文: Disomy frequency of sex chromosome (0.9%、0.%), chromosome (0.0%、0.09%), chromosome (0.8%、0.0%)and rates of dipoidy in severe oligozoospermic men (0. %、0.09%) were higher than that in control group (P<0.00).
中文: 在严重少精症组,精子性染色体二体率(0.9%、0.%)、 号染色体二体率(0.0%、0.09%)、号染色体二体率(0.8%、0.0%)、二倍体率(0. %、0.09%)明显高于对照组,有显著性差异(P<0.00);
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英文: Disomy frequency of sex chromosome(. %、0.%)and rates of dipoidy (0. % 、0.09%) in obstructive azoospermic men were higher that in control group (P<0.00).
中文: 在阻塞性无精症组,性染色体二体率(. %、0.%)、二倍体率(0. %、0.09%)明显高于对照组,有显著性差异(P<0.00)。
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英文: Results: Frequency of sex chromosome aneuploidy was clearly increasing in oligospermic men(0.8%, 0.% ,P<0.00) and general expressions were disomy XY, XX and YY.
中文: 果:少精症组精子性染色体非整倍体发生率明显升高(0.8%、0.%,P<0.00),常见的形式为精子XY二体、XX二体以及YY二体;
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英文: Results: In group B the frequencies of spermatozoon disomy for chromosomes including X,Y and 9 were 0. 0% and 0. 0% respectively. The percentages were not significantly different from those of group C (0.%,0%).
中文: 果 :B组精子 X、Y、和 8号染色体的二体频率分别为 0 . 0 %、0 . 0 % ,与 C组 ( 0 . %、0 % )相比差别无显著性 ;
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