Parental mosaicism in de novo neurodevelopmental diseases Li Shu 1 2 3, Qianjun Zhang 4 5 6, Qi Tian 1 2, Sai Yang 7, Xingwang Peng 8, Xiao Mao 1 2, Liming Yang 7, Juan Du 4 5 6, Hua Wang Am J Med Genet A. 2021 Jul;185(7):2119-2125. doi: 10.1002/ajmg.a.62174.Epub 2021 Apr 14.
Pre One:Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and miceChaofeng Tu 1, Jiangshan Cong 2, Qianjun Zhang 1, Xiaojin He 3, Rui Zheng 4, Xiaoxuan Yang 5, Yang Gao 3, Huan Wu 3, Mingrong Lv 3, Yayun Gu 6, Shuai Lu 6, Chunyu Liu 2, Shixiong Tian 2, Lanlan Meng 7, Weili Wang 5, Chen Tan 5, Hongchuan Nie 7, Dongyan Li 5, Huan Zhang 7, Fei Gong 1, Liang Hu 1, Guangxiu Lu 7, Wenming Xu 4, Ge Lin 1, Feng Zhang 2, Yunxia Cao 8, Yue-Qiu Tan 9 Am J Hum Gene
Next One:Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD. Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G, Zhang Q, Tan YQ.Hum Genet. 2020 Feb;139(2):257-271. doi: 10.1007/s00439-020-02110-0. Epub 2020 Jan 16.