Showing results (31-40 of 42) with videos related to
Sort By:
Pageof 5
Frontiers in Pediatrics|October 4, 2024
Novel loss-of-function variants in <i>WDR26</i> cause Skraban-Deardorff syndrome in two Chinese patientsQi Yang, Xunzhao Zhou, Sheng Yi, et al.International Journal of Laboratory Hematology|September 5, 2022
Reference intervals for erythrocyte parameters and hemoglobin electrophoresis parameters for young children in GuangxiChaofan Zhou, Sheng He, Dun Liu, et al.Gene|February 26, 2018
Molecular characterization of α- and β-thalassemia in the Yulin region of Southern ChinaSheng He, Jihui Li, Dong Ming Li, et al.International Journal of General Medicine|November 25, 2024
Epidemiology of Congenital Heart Defects in Perinatal Infants in Guangxi, ChinaZhenren Peng, Jie Wei, Xiuning Huang, et al.Biochemical Genetics|January 24, 2026
Clinical and Molecular Characterization of Five Additional Individuals With SATB2-Associated Syndrome in GuangxiSheng Yi, Qinle Zhang, Fei Chen, et al.Journal of Molecular Neuroscience : MN|May 10, 2022
De Novo SMARCC2 Variant in a Chinese Woman with Coffin-Siris Syndrome 8: a Case Report with Mild Intellectual Disability and EndocrinopathySheng Yi, Mengting Li, Qi Yang, et al.Frontiers in Pediatrics|August 7, 2023
Epidemiology of birth defects based on a birth defects surveillance system in southwestern China and the associated risk factorsZhenren Peng, Jie Wei, Biyan Chen, et al.Scientific Reports|July 26, 2019
Etiology and Outcome of non-immune Hydrops Fetalis in Southern China: report of 1004 casesDahua Meng, Qifei Li, Xuehua Hu, et al.Human Mutation|July 10, 2019
LOVD-DASH: A comprehensive LOVD database coupled with diagnosis and an at-risk assessment system for hemoglobinopathiesLi Zhang, Qianqian Zhang, Yaohua Tang, et al.European Journal of Human Genetics : EJHG|September 5, 2020
NGS-based spinal muscular atrophy carrier screening of 10,585 diverse couples in China: a pan-ethnic studySumin Zhao, Wanyang Wang, Yaoshen Wang, et al.Pageof 5