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Studies in Health Technology and Informatics|June 30, 2021
Effect of PSSE on postural sway in AIS using center of pressureM Selthafner, X C Liu, F Ellis, et al.Genes|December 23, 2022
Fragile X-Associated Neuropsychiatric Disorders (FXAND) in Young Fragile X Premutation CarriersRamkumar Aishworiya, Dragana Protic, Si Jie Tang, et al.Clinical Medicine Insights. Case Reports|February 23, 2019
A Case of Critical Calcified Innominate Artery Stenosis Successfully Treated With the Shockwave LithoplastyCesare Tripolino, Placido Grillo, Eliezer Joseph Tassone, et al.EURASIP Journal on Bioinformatics & Systems Biology|February 15, 2017
Analysis of miRNA, mRNA, and TF interactions through network-based methodsPietro H Guzzi, Maria Teresa Di Martino, Pierosandro Tagliaferri, et al.Spine Deformity|February 25, 2024
Correlation of transverse rotation of the spine using surface topography and 3D reconstructive radiography in children with idiopathic scoliosisMilan Patel, Xue-Cheng Liu, Channing Tassone, et al.Otolaryngology--Head and Neck Surgery : Official Journal of American Academy of Otolaryngology-Head and Neck Surgery|May 26, 2023
Trends in Positive Surgical Margins in cT3-T4 Oral Cavity Squamous Cell CarcinomaKavita Prasad, Michael C Topf, Stephanie Clookey, et al.Frontiers in Genetics|November 23, 2017
Prenatal Diagnosis of Fragile X: Can a Full Mutation Allele in the FMR1 Gene Contract to a Normal Size?Esther Manor, Azhar Jabareen, Nurit Magal, et al.Molecules (Basel, Switzerland)|April 3, 2019
Structural Comparison of Enterococcus faecalis and Human Thymidylate Synthase Complexes with the Substrate dUMP and Its Analogue FdUMP Provides Hints about Enzyme Conformational VariabilitiesCecilia Pozzi, Stefania Ferrari, Rosaria Luciani, et al.Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|December 30, 2006
Tremor/ataxia syndrome and fragile X premutation: diagnostic caveatsD Z Loesch, L Litewka, A Churchyard, et al.American Journal of Medical Genetics. Supplement|January 1, 1990
Molecular study of parental origin of extra chromosome 21 in regular and de novo translocation trisomiesC Brahe, F Tassone, A Moscetti, et al.Pageof 139