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Human Molecular Genetics|January 3, 2018
Familial paroxysmal kinesigenic dyskinesia is associated with mutations in the KCNA1 geneXiao-Meng Yin, Jing-Han Lin, Li Cao, et al.
Brain : a Journal of Neurology|December 11, 2019
Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremorQi-Ying Sun, Qian Xu, Yun Tian, et al.
Cancer Cell|September 5, 2017
LMO1 Synergizes with MYCN to Promote Neuroblastoma Initiation and MetastasisShizhen Zhu, Xiaoling Zhang, Nina Weichert-Leahey, et al.
Translational Neurodegeneration|August 5, 2020
GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control studyHong-Xu Pan, Yu-Wen Zhao, Jun-Pu Mei, et al.
Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz|February 9, 2020
[Persons with migration background in the German National Cohort (NAKO)-sociodemographic characteristics and comparisons with the German autochthonous population]Christian Wiessner, Thomas Keil, Lilian Krist, et al.
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