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Dive into the research topics of 'Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature'. Together they form a unique fingerprint.- Sort by
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Zilong Qiu, Wan Ting Chang, Yu Ching Chou, Kuo Chang Wen, Yang Ziying, Kayiu Yuen, Xiongying Cai, Tung yao Chang, Hung Cheng Lai, Pi Lin Sung
Research output: Contribution to journal › Article › peer-review