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Frontiers in Psychology|August 23, 2023
Parenting stress and Chinese preschoolers' approaches to learning: a moderated mediation model of authoritative parenting and household residencyJinghui Zhao, Yizhen Fan, Ziqin Liu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 14, 2020
[Identification of a novel AGPAT2 variant in a Chinese patient with congenital generalized lipodystrophy type 1]Yiping Wang, Yanli Zhu, Jinli Bai, et al.Small (Weinheim an Der Bergstrasse, Germany)|March 9, 2023
The Inducement and "Rejuvenation" of Li Dendrites by Space Confinement and Positive Fe/Co-SitesZiqin Liu, Xin Dong, Jing Wen, et al.Journal of Colloid and Interface Science|June 12, 2023
The inhibited Li dendrite growth via bulk/liquid dual-phase modulationXin Dong, Ziqin Liu, Kaiquan He, et al.Translational Pediatrics|June 30, 2021
A novel frameshift mutation in the FGD1 gene causing Aarskog-Scott syndrome patient with hypogonadism: a case reportHongshuai Jia, Tiantian Ma, Ziqin Liu, et al.Carbohydrate Polymers|April 23, 2014
Post-crosslinking modification of thermoplastic starch/PVA blend films by using sodium hexametaphosphateZiqin Liu, Yan Dong, Haitao Men, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|March 11, 2026
[Genetic analysis of a Chinese pedigree affected with Isolated growth hormone deficiency due to variant of CHRHR gene]Hui Yin, Bingyan Cao, Ziqin Liu, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|July 10, 2022
[Clinical and genetic analysis of a patient with isolated 17,20 lyase deficiency presenting with pubertal gynecomastia]Hui Yin, Xiaobo Chen, Ziqin Liu, et al.Molecular Medicine Reports|February 8, 2014
A correlation analysis of miRNA‑34a and its predicted target genes in leukemiaRuihong Tang, Juanjuan Li, Mei Yue, et al.Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 1, 2026
[Clinical and genetic analysis of a child with 46,XX male phenotype due to SOX3 gene duplication]Xiou Wang, Fuying Song, Ziqin Liu, et al.Pageof 5