Investigating the impact of vulnerability datasets on deep learning-based vulnerability detectors

por Liu, Lili, Li, Zhen, Wen, Yu, Chen, Penglong
Publicado 2022

Case report: genetic analysis of a novel frameshift mutation in FMR1 gene in a Chinese family

por Jin, Chunlei, Zhang, Xiangdong, Lei, Qiang, Chen, Penglong, Hu, Hui, Shen, Shuangshuang, Liu, Jiao, Ye, Shixuanbao
Publicado 2023

Paternal Low-Level Mosaicism-Caused SATB2-Associated Syndrome

por Qian, Yeqing, Liu, Jiao, Yang, Yanmei, Chen, Min, Jin, Chunlei, Chen, Penglong, Lei, Yongliang, Pan, Hangyi, Dong, Minyue
Publicado 2019

Case Report: Prenatal Diagnosis of a Fetus With Harlequin Ichthyosis Identifies Novel Compound Heterozygous Variants: A Case Report

por Liu, Jiao, Zhang, Xingyu, Wang, Weilan, Lan, Xiaofang, Dong, Minyue, Yan, Kai, Lei, Yongliang, Chen, Penglong, Yang, Mufeng, Shan, Qunda, Jin, Chunlei
Publicado 2021