全基因组学关联研究所产生的数据结果是巨大的，但是很少能直接鉴别出突变和病症之间的功能关系。
The output of genome-wide association studies is vast, yet it is rarely straightforward to identify the functional connection between a variant and a disorder.
目前报道的生物素酶基因突变超过80余种，全羧化酶合成酶基因突变20多种。
Thus far more than 80 mutations in the gene of biotinidase and more than 20 mutations in the holocarboxylase synthetase gene have been reported.
摘要目的探讨y染色体微缺失和突变时，两男性个体间的全同胞关系鉴定。
Abstract: Objective To explore the identification method of full sibling between two males with microdeletion and mutation of Y chromosome.
对水稻脂质氧化酶（LOX）同工酶缺失的单体及聚合体人工老化实验研究表明：不同LOX的缺失突变体之间，以LOX-1，LOX-2、LOX-3全缺的D1308、D1311的发芽率始终最高，老化指数最低；
It is shown through accelerated aging tests that among all materials D1308, D1311 with null- LOX-1, LOX-2 and LOX-3 have the highest germination ratio and the lowest aging index ;
对水稻脂质氧化酶（LOX）同工酶缺失的单体及聚合体人工老化实验研究表明：不同LOX的缺失突变体之间，以LOX-1，LOX-2、LOX-3全缺的D1308、D1311的发芽率始终最高，老化指数最低；
It is shown through accelerated aging tests that among all materials D1308, D1311 with null- LOX-1, LOX-2 and LOX-3 have the highest germination ratio and the lowest aging index ;
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