Showing results (1-10 of 533) with videos related to

Sort By:
Pageof 54
Journal of Clinical Research in Pediatric Endocrinology|August 27, 2019
A Novel Missense Mutation in Human Receptor Roundabout-1 (ROBO1) Gene Associated with Pituitary Stalk Interruption SyndromeZiqin Liu, Xiaobo Chen
Translational Pediatrics|May 13, 2022
Whole-exome sequencing establishes a diagnosis of Alstrom syndrome: a case reportZiqin Liu, Xiaobo Chen
Translational Pediatrics|August 25, 2021
Progressive pseudorheumatoid dysplasia: a case series reportZiqin Liu, Xiaobo Chen
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|October 9, 2021
[Siblings Seckel's syndrome 1 caused by ATR gene variants in a sibpair]Mingfang Qiu, Ziqin Liu, Xiaobo Chen
Frontiers in Pediatrics|September 5, 2022
The etiology and clinical features of non-CAH primary adrenal insufficiency in childrenZiqin Liu, Yi Liu, Kang Gao, 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.
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.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 4, 2023
Diagnostic model based on multiple factors for girls with central precocious pubertyZiqin Liu, Qinwei Song
Pageof 54