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Showing results (151-160 of 158) with videos related to

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Human Genetics|November 8, 2023
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes ProjectFeifan Xiao, Bingbing Wu, Chenbin Dong, et al.
Nature Medicine|May 20, 2026
Pathogenic germline variations and cancer risks in pediatric patients referred for genetic testingHuijun Wang, Xinran Dong, Feifan Xiao, et al.
Cellular and Molecular Gastroenterology and Hepatology|January 30, 2022
The miR-23b/27b/24-1 Cluster Inhibits Hepatic Fibrosis by Inactivating Hepatic Stellate CellsLin-Yan Wan, Hu Peng, Yi-Ran Ni, et al.
Kidney International Reports|November 29, 2023
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome ProjectZhelan Huang, Qian Shen, Bingbing Wu, et al.
Human Mutation|January 27, 2021
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes projectHuijun Wang, Feifan Xiao, Xinran Dong, et al.
Journal of Medical Genetics|May 20, 2022
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes ProjectHuijun Wang, Feifan Xiao, Yanyan Qian, et al.
Critical Care Medicine|May 3, 2021
Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes ProjectBingbing Wu, Wenqing Kang, Yingyuan Wang, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|July 19, 2022
Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome ProjectTiantian Xiao, Jin Wang, Huijun Wang, et al.
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Showing results (151-160 of 158) with videos related to

Sort By:
Pageof 16
You have reached the last page of results.This site can display upto 158 results.
Human Genetics|November 8, 2023
Genetic spectrums and clinical profiles of critically ill neonates with congenital auricular deformity in the China Neonatal Genomes ProjectFeifan Xiao, Bingbing Wu, Chenbin Dong, et al.
Nature Medicine|May 20, 2026
Pathogenic germline variations and cancer risks in pediatric patients referred for genetic testingHuijun Wang, Xinran Dong, Feifan Xiao, et al.
Cellular and Molecular Gastroenterology and Hepatology|January 30, 2022
The miR-23b/27b/24-1 Cluster Inhibits Hepatic Fibrosis by Inactivating Hepatic Stellate CellsLin-Yan Wan, Hu Peng, Yi-Ran Ni, et al.
Kidney International Reports|November 29, 2023
Genetic Spectrum of Congenital Anomalies of the Kidney and Urinary Tract in Chinese Newborn Genome ProjectZhelan Huang, Qian Shen, Bingbing Wu, et al.
Human Mutation|January 27, 2021
Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes projectHuijun Wang, Feifan Xiao, Xinran Dong, et al.
Journal of Medical Genetics|May 20, 2022
Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes ProjectHuijun Wang, Feifan Xiao, Yanyan Qian, et al.
Critical Care Medicine|May 3, 2021
Application of Full-Spectrum Rapid Clinical Genome Sequencing Improves Diagnostic Rate and Clinical Outcomes in Critically Ill Infants in the China Neonatal Genomes ProjectBingbing Wu, Wenqing Kang, Yingyuan Wang, et al.
Archives of Disease in Childhood. Fetal and Neonatal Edition|July 19, 2022
Aetiology and outcomes of prolonged neonatal jaundice in tertiary centres: data from the China Neonatal Genome ProjectTiantian Xiao, Jin Wang, Huijun Wang, et al.
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