Yongjia Yang
10PUBLICATIONS
11CO-AUTHORS
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Publications (10)
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|Dec 11, 2025
Recessive SMC5 Variants in a Family with Near-Tetraploidy/Mosaic Variegated Aneuploidy.Yongjia Yang, Nian Li, Cheng Liu
|Jul 16, 2025
AUTS2 disruption underlies radioulnar synostosis and skeletal dysmorphogenesis: evidence from four unrelated cases.Cheng Liu, Fang Shen, Mei Deng
|Dec 02, 2022
Novel Loss of Function (G15D) Mutation on RAC2 in a Family with Combined Immunodeficiency and Increased Levels of Immunoglobulin G, A, and E.Xiaojun Duan, Fang Shen, Yafei Deng
|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
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