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Scientific Reports|March 18, 2018
An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosisYoji Ogura, Kazuki Takeda, Ikuyo Kou, et al.Human Molecular Genetics|October 12, 2018
TBX6 compound inheritance leads to congenital vertebral malformations in humans and miceNan Yang, Nan Wu, Ling Zhang, et al.Clinical and Experimental Rheumatology|February 16, 2019
Efficacy of bisphosphonates in patients with synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome: a prospective open studyChen Li, Yanxue Zhao, Yuzhi Zuo, et al.Nature Communications|February 6, 2024
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spineSen Zhao, Hengqiang Zhao, Lina Zhao, et al.Scientific Reports|August 3, 2018
A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosisIkuyo Kou, Kota Watanabe, Yohei Takahashi, et al.Spine|February 11, 2017
Genetic Polymorphism of LBX1 Is Associated With Adolescent Idiopathic Scoliosis in Northern Chinese Han PopulationSen Liu, Nan Wu, Yuzhi Zuo, et al.Human Genetics|July 19, 2018
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to diseaseJiaqi Liu, Yangzhong Zhou, Sen Liu, et al.The Journal of Clinical Investigation|November 14, 2023
Impaired glycine neurotransmission causes adolescent idiopathic scoliosisXiaolu Wang, Ming Yue, Jason Pui Yin Cheung, et al.Journal of Genetics and Genomics = Yi Chuan Xue Bao|May 19, 2021
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short statureXin Fan, Sen Zhao, Chenxi Yu, et al.Journal of Human Genetics|December 13, 2019
Identification of novel FBN1 variations implicated in congenital scoliosisMao Lin, Sen Zhao, Gang Liu, et al.Pageof 24