Showing 1 - 1 results of 1 for search 'Guangxian Yang', query time: 0.01s Refine Results
  1. 1
    Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

    Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss by Guangxian Yang, Yi Yin, Zhiping Tan, Jian Liu, Xicheng Deng, Yifeng Yang

    Published 2021
    Connect to this object online.
    Book
    Save to List
    Saved in:

Search Tools: