Showing results (211-220 of 218) with videos related to
Sort By:
Pageof 22
You have reached the last page of results.This site can display upto 218 results.
Human Molecular Genetics|June 28, 2020
C1orf194 deficiency leads to incomplete early embryonic lethality and dominant intermediate Charcot-Marie-Tooth disease in a knockout mouse modelCheng Huang, Zong Rui Shen, Jin Huang, et al.Journal of Medical Genetics|June 2, 2016
A splicing mutation in VPS4B causes dentin dysplasia IQi Yang, Dong Chen, Fu Xiong, et al.NPJ Breast Cancer|August 22, 2020
Long-term anti-inflammatory diet in relation to improved breast cancer prognosis: a prospective cohort studyKang Wang, Jia-Zheng Sun, Qian-Xue Wu, et al.Human Mutation|September 30, 2016
Mutation in SSUH2 Causes Autosomal-Dominant Dentin Dysplasia Type IFu Xiong, Zhisong Ji, Yanhui Liu, et al.BMC Medicine|May 28, 2025
Transarterial chemoembolization plus apatinib for unresectable hepatocellular carcinoma: a multicenter, randomized, open-label, phase III trialXue-Feng Kan, Bin Liang, Xiao-Lin Zhang, et al.Brain : a Journal of Neurology|June 15, 2019
Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth diseaseShun-Chang Sun, Di Ma, Mei-Yi Li, et al.BMJ Paediatrics Open|June 29, 2023
Parental detection of neonatal jaundice using a low-cost colour card: a multicentre prospective studyGuochang Xue, Huali Zhang, Xuexing Ding, et al.Ebiomedicine|September 4, 2017
Rapid Targeted Next-Generation Sequencing Platform for Molecular Screening and Clinical Genotyping in Subjects with HemoglobinopathiesXuan Shang, Zhiyu Peng, Yuhua Ye, et al.Pageof 22