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Human Mutation|February 10, 2022
Diagnosis and follow-up of glycogen storage disease (GSD) type VI from the largest GSD center in ChinaXiaomei Luo, Ying Duan, Di Fang, et al.
Journal of Affective Disorders|August 24, 2019
Altered biochemical metabolism and its lateralization in the cortico-striato-cerebellar circuit of unmedicated bipolar II depressionShunkai Lai, Shuming Zhong, Yanyan Shan, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 20, 2016
Targeted exome sequencing identifies novel compound heterozygous mutations in P3H1 in a fetus with osteogenesis imperfecta type VIIIYanru Huang, Libin Mei, Weigang Lv, et al.
Journal of Affective Disorders|July 13, 2019
Abnormal resting-state regional homogeneity in unmedicated bipolar II disorderShaojuan Qiu, Feng Chen, Guanmao Chen, et al.
The Journal of Molecular Diagnostics : JMD|February 27, 2023
Deep Intronic PAH Variants Explain Missing Heritability in HyperphenylalaninemiaXiaomei Luo, Ruifang Wang, Yu Sun, et al.
Journal of Magnetic Resonance Imaging : JMRI|March 17, 2023
A Multicenter Study on Preoperative Assessment of Lymphovascular Space Invasion in Early-Stage Cervical Cancer Based on Multimodal MR RadiomicsYu Wu, Shuxing Wang, Yiqing Chen, et al.
Taiwanese Journal of Obstetrics & Gynecology|March 8, 2021
Chromosomal microarray analysis in fetuses with high-risk prenatal indications: A retrospective study in ChinaXiaomei Luo, Hong Zhu, Lili Wang, et al.
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