日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

The pathogenic mechanism of syndactyly type V identified in a Hoxd13Q50R knock-in mice

Hoxd13Q50R 基因敲入小鼠鉴定出 V 型并指畸形的致病机制

Han Wang #, Xiumin Chen #, Xiaolu Meng, Yixuan Cao, Shirui Han, Keqiang Liu, Ximeng Zhao, Xiuli Zhao, Xue Zhang

Panoramic variation analysis of a family with neurodevelopmental disorders caused by biallelic loss-of-function variants in TMEM141, DDHD2, and LHFPL5

因 TMEM141、DDHD2 和 LHFPL5 双等位基因功能丧失变异导致的神经发育障碍家族的全景变异分析

Liwei Sun #, Xueting Yang #, Amjad Khan #, Xue Yu, Han Zhang, Shirui Han, Xiaerbati Habulieti, Yang Sun, Rongrong Wang, Xue Zhang

Novel Compound Heterozygous Mutations in TTI2 Cause Syndromic Intellectual Disability in a Chinese Family

TTI2 新型复合杂合突变导致中国家庭出现综合征性智力障碍

Rongrong Wang, Shirui Han, Hongyan Liu, Amjad Khan, Habulieti Xiaerbati, Xue Yu, Jia Huang, Xue Zhang