نتائج البحث - Wang, Chengrong
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Whole-exome sequencing as a powerful tool for identifying genetic causes in a patient with POLG-related disorders and phenylketonuria حسب Li, Lin, Zhao, Jin-Qi, Wang, Chengrong, Yang, Nan, Gong, Li-Fei, Yang, Hai-He, Yin, Chenghong, Kong, Yuan-Yuan
منشور في 2019نص -
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Assessment of evidence on reported non-genetic risk factors of congenital heart defects: the updated umbrella review حسب Nie, Xiaolu, Liu, Xiaohang, Wang, Chen, Wu, Zehao, Sun, Zimo, Su, Jian, Yan, Ruohua, Peng, Yaguang, Yang, Yuxuan, Wang, Chengrong, Cai, Siyu, Liu, Yali, Yu, Huanling, Wu, Qingqing, Peng, Xiaoxia, Yin, Chenghong
منشور في 2022نص