Yu Zheng
6PUBLICATIONS
14CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (6)
Sort by Publication Date:
|Jan 13, 2022
Case series of congenital pseudarthrosis of the tibia unfulfilling neurofibromatosis type 1 diagnosis: 21% with somatic NF1 haploinsufficiency in the periosteum.Yu Zheng, Guanghui Zhu, Yaoxi Liu
|Dec 25, 2021
A genotype and phenotype analysis of SMAD6 mutant patients with radioulnar synostosis.Fang Shen, Yongjia Yang, Pengcheng Li
|Jul 23, 2021
Expanding the genotypes and phenotypes for 19 rare diseases by exome sequencing performed in pediatric intensive care unit.Juan Liu, Yu Zheng, Jiaotian Huang
|Jun 11, 2019
Correction: SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.Yongjia Yang, Yu Zheng, Wangming Li
|May 30, 2019
SMAD6 is frequently mutated in nonsyndromic radioulnar synostosis.Yongjia Yang, Yu Zheng, Wangming Li
Pageof 1