《中国科技论文在线》网络电子期刊—论文页面 关 键 词： 医学遗传学；Apert综合征；FGFR2基因；突变 [gap=1494]Key words: medical genetics; Apert syndrome; FGFR2 gene; mutation
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One3, looking at about 2,000 postmenopausal women and a similar number of controls, also identified genetic variants in the FGFR2 gene associated with increased cancer risk2.
其中一项，大约2，000个绝经期妇女和相同数量的对照组，也确定了FGFR2的基因变异与癌症危险性增加有关。
The only gene with pathogenic variants in more than one case was FGFR2, seen in two fetuses with features suggestive of skeletal dysplasia.
FGFR2基因是唯一一个在不止一个病例中具有致病性变异的基因（两个胎儿具有骨骼发育异常的特点）。
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