However, FGFR2 were located uniformly in the cytoplasm of the oocytes and preimplantation embryos.
FGFR2阳性反应较均匀分布于卵母细胞和植入前胚的胞质。
Researchers identified four genes called FGFR2, TNRC9, MAP3K1 and LSP1 as increasing risk of breast cancer.
研究人员确认了四种基因能增加乳腺癌患病风险，分别称之为FGFR2、TNRC9、MAP3K1 和LSP1。
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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