Prenatal case of RIT1 mutation associated Noonan syndrome by whole exome sequencing (WES) and review of the literature by 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

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