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Journal of Medical Genetics|December 16, 2020
Phenotype and genotype spectra of a Chinese cohort with nephronophthisis-related ciliopathyXiaoshan Tang, Cuihua Liu, Xiaorong Liu, et al.
European Journal of Medical Genetics|September 6, 2020
Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohortShuzhen Sun, Linan Xu, Yunli Bi, et al.
BMC Medical Genomics|October 26, 2021
Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohortXue Yang, Yaqi Li, Ye Fang, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 22, 2022
Genetic spectrum of CAKUT and risk factors for kidney failure: a pediatric multicenter cohort studyJia-Lu Liu, Xiao-Wen Wang, Cui-Hua Liu, et al.
World Journal of Pediatrics : WJP|June 1, 2021
Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease DatabaseJia-Lu Liu, Qian Shen, Ming-Yan Wu, et al.
Clinical Genetics|July 23, 2019
Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration systemJia Rao, Xiaorong Liu, Jianhua Mao, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 9, 2018
[Discussion on the standard of clinical genetic testing report and the consensus of gene testing industry]Hui Huang, Yiping Shen, Weihong Gu, et al.
Phenomics (Cham, Switzerland)|March 20, 2023
Genetic Architecture of Childhood Kidney and Urological Diseases in ChinaYe Fang, Hua Shi, Tianchao Xiang, et al.
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