Search Results - Peiwei Zhao

  • Showing 1 - 2 results of 2
Refine Results
  1. 1
    Cover Image

    Severe congenital microcephaly with 16p13.11 microdeletion combined with NDE1 mutation, a case report and literature review by Li Tan, Bo Bi, Peiwei Zhao, Xiaonan Cai, Chunhui Wan, Jianbo Shao, Xuelian He

    Published 2017
    Connect to this object online.
    Book

    Save to List
    Saved in:
  2. 2
    Cover Image

    Activated phosphoinositide 3-kinase δ syndrome caused by PIK3CD mutations: expanding the phenotype by Peiwei Zhao, Juan Huang, Huicong Fu, Jiali Xu, Tianhong Li, Xiankai Zhang, Qingjie Meng, Lei Zhang, Li Tan, Wen Zhang, Hebin Chen, Xiaoxia Lu, Yan Ding, Xuelian He

    Published 2024
    Connect to this object online.
    Book

    Save to List
    Saved in:

Search Tools: