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Showing results (991-1000 of 1,008) with videos related to

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Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Medicina|August 12, 2025
[Prevention and treatment of infections in phlebology and lymphology]Fanny Rodríguez Santos, Oscar Bottini, Yanina Nuccetelli, et al.
Epilepsia|January 21, 2021
The severe epilepsy syndromes of infancy: A population-based studyKatherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.
Annals of Clinical and Translational Neurology|March 28, 2024
Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing aloneRhett G Marchant, Samantha J Bryen, Melanie Bahlo, et al.
Nature Communications|March 16, 2026
Mining antibody functionality via AI-guided structural landscape profilingStanislav S Terekhov, Nikita V Ivanisenko, Nan Zhang, et al.
Scientific Reports|June 22, 2017
Corrigendum: Double-flow focused liquid injector for efficient serial femtosecond crystallographyDominik Oberthuer, Juraj Knoška, Max O Wiedorn, et al.
Nature|April 29, 2021
A molecular single-cell lung atlas of lethal COVID-19Johannes C Melms, Jana Biermann, Huachao Huang, et al.
Scientific Reports|March 17, 2017
Double-flow focused liquid injector for efficient serial femtosecond crystallographyDominik Oberthuer, Juraj Knoška, Max O Wiedorn, et al.
Human Mutation|March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported PatientsBobby G Ng, Sergey A Shiryaev, Daisy Rymen, et al.
Pageof 101

Showing results (991-1000 of 1,008) with videos related to

Sort By:
Pageof 101
Nature Genetics|May 1, 2012
Mutations in the RNA exosome component gene EXOSC3 cause pontocerebellar hypoplasia and spinal motor neuron degenerationJijun Wan, Michael Yourshaw, Hafsa Mamsa, et al.
European Journal of Medical Genetics|July 8, 2022
Unclassified white matter disorders: A diagnostic journey requiring close collaboration between clinical and laboratory servicesC A Stutterd, A Vanderver, P J Lockhart, et al.
Medicina|August 12, 2025
[Prevention and treatment of infections in phlebology and lymphology]Fanny Rodríguez Santos, Oscar Bottini, Yanina Nuccetelli, et al.
Epilepsia|January 21, 2021
The severe epilepsy syndromes of infancy: A population-based studyKatherine B Howell, Jeremy L Freeman, Mark T Mackay, et al.
Annals of Clinical and Translational Neurology|March 28, 2024
Genome and RNA sequencing boost neuromuscular diagnoses to 62% from 34% with exome sequencing aloneRhett G Marchant, Samantha J Bryen, Melanie Bahlo, et al.
Nature Communications|March 16, 2026
Mining antibody functionality via AI-guided structural landscape profilingStanislav S Terekhov, Nikita V Ivanisenko, Nan Zhang, et al.
Scientific Reports|June 22, 2017
Corrigendum: Double-flow focused liquid injector for efficient serial femtosecond crystallographyDominik Oberthuer, Juraj Knoška, Max O Wiedorn, et al.
Nature|April 29, 2021
A molecular single-cell lung atlas of lethal COVID-19Johannes C Melms, Jana Biermann, Huachao Huang, et al.
Scientific Reports|March 17, 2017
Double-flow focused liquid injector for efficient serial femtosecond crystallographyDominik Oberthuer, Juraj Knoška, Max O Wiedorn, et al.
Human Mutation|March 3, 2016
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported PatientsBobby G Ng, Sergey A Shiryaev, Daisy Rymen, et al.
Pageof 101