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Science Robotics|May 17, 2023
A hierarchical sensorimotor control framework for human-in-the-loop robotic handsLucia Seminara, Strahinja Dosen, Fulvio Mastrogiovanni, et al.Diagnostic and Interventional Radiology (Ankara, Turkey)|November 9, 2018
Abnormal subcortical activity in congenital mirror movement disorder with RAD51 mutationPınar Demirayak, Onur Emre Onat, Aslıhan Örs Gevrekci, et al.Neuroimage|April 8, 2018
Homozygous LAMC3 mutation links to structural and functional changes in visual attention networksBuse M Urgen, Yasemin Topac, F Seyhun Ustun, et al.Brain and Behavior|June 14, 2021
Cortical connectivity in the face of congenital structural changes-A case of homozygous LAMC3 mutationPinar Demirayak, Kader Karli Oguz, Fatma Seyhun Ustun, et al.Cognition|August 11, 2024
Representations of the relative proportions of body part widthLettie Wareing, Lisa P Y Lin, Megan Rose Readman, et al.Genome Research|September 3, 2011
Homozygosity mapping and targeted genomic sequencing reveal the gene responsible for cerebellar hypoplasia and quadrupedal locomotion in a consanguineous kindredSuleyman Gulsuner, Ayse Begum Tekinay, Katja Doerschner, et al.Nature Genetics|May 17, 2011
Recessive LAMC3 mutations cause malformations of occipital cortical developmentTanyeri Barak, Kenneth Y Kwan, Angeliki Louvi, et al.Pageof 11