Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short Stature
Baoheng Gui(Cincinnati Children's Hospital Medical Center), Jianguo Zhang(Chinese Academy of Medical Sciences & Peking Union Medical College), Xi Cheng(Nantong University), Chunrong Gui(Guangxi Medical University), Lina Zhao(Tianjin Medical University General Hospital), Chenxi Yu(Universidade de São Paulo), Zihui Yan(Chinese Academy of Medical Sciences & Peking Union Medical College), Huizi Wang(Kunming University of Science and Technology), Yuchen Niu(Harbin Engineering University), Chunxiu Gong(Beijing Children’s Hospital), Hengqiang Zhao(Baylor College of Medicine), Yi Wang(ITRI International), Chuan Li(Guangxi Medical University), Xiaoxin Li(Chinese Academy of Medical Sciences & Peking Union Medical College), Sen Zhao(Hebei Medical University), Yanning Song(Capital Medical University), Jiashen Shao(Chinese Academy of Medical Sciences & Peking Union Medical College), Xianda Wei(Guangxi Medical University), Zhi Gang Zhao(Chinese Academy of Medical Sciences & Peking Union Medical College), Haiyang Zheng(Guangxi Medical University), Bobo Xie(Guangxi Maternal and Child Health Hospital), Shaoke Chen(Guangxi Maternal and Child Health Hospital), Zhengye Zhao(Chinese Academy of Medical Sciences & Peking Union Medical College), Jiachen Lin(Zhejiang University)
Cited by 5
Related Papers
Biparental Inheritance of Mitochondrial DNA in Humans
|Proceedings of the National Academy of Sciences|2018|451
Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective
|Hormone Research in Paediatrics|2019|345
Haplotype-resolved genome of diploid ginger (<i>Zingiber officinale</i>) and its unique gingerol biosynthetic pathway
|Horticulture Research|2021|132
TBX6-associated congenital scoliosis (TACS) as a clinically distinguishable subtype of congenital scoliosis: further evidence supporting the compound inheritance and TBX6 gene dosage model
|Genetics in Medicine|2019|94
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome
|The American Journal of Human Genetics|2021|90