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The Journal of Molecular Diagnostics : JMD|June 1, 2020
Long-Molecule Sequencing: A New Approach for Identification of Clinically Significant DNA Variants in α-Thalassemia and β-Thalassemia CarriersLiangpu Xu, Aiping Mao, Hui Liu, et al.Proceedings of the National Academy of Sciences of the United States of America|November 28, 2018
Biparental Inheritance of Mitochondrial DNA in HumansShiyu Luo, C Alexander Valencia, Jinglan Zhang, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 27, 2019
Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosisHuilin Wang, Zirui Dong, Rui Zhang, et al.Frontiers in Cell and Developmental Biology|May 3, 2021
Heterozygous Recurrent Mutations Inducing Dysfunction of ROR2 Gene in Patients With Short StatureBaoheng Gui, Chenxi Yu, Xiaoxin Li, et al.Frontiers in Endocrinology|September 30, 2021
Whole Exome Sequencing Uncovered the Genetic Architecture of Growth Hormone Deficiency PatientsChenxi Yu, Bobo Xie, Zhengye Zhao, et al.Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureXin Fan, Sen Zhao, Chenxi Yu, et al.Human Molecular Genetics|October 18, 2017
Biallelic mutations in the ferredoxin reductase gene cause novel mitochondriopathy with optic atrophyYanyan Peng, Deepali N Shinde, C Alexander Valencia, et al.Pageof 4