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）。
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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