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Medical Physics|May 25, 2019
AAPM task group 224: Comprehensive proton therapy machine quality assuranceBijan Arjomandy, Paige Taylor, Christopher Ainsley, et al.
Human Mutation|October 26, 2017
Expanding the genetic architecture and phenotypic spectrum in the skeletal ciliopathiesWenjuan Zhang, S Paige Taylor, Hayley A Ennis, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|March 20, 2021
Report dose-to-medium in clinical trials where available; a consensus from the Global Harmonisation Group to maximize consistencyStephen F Kry, Jessica Lye, Catharine H Clark, et al.
Physics and Imaging in Radiation Oncology|December 25, 2019
Remote beam output audits: a global assessment of results out of toleranceStephen F Kry, Christine B Peterson, Rebecca M Howell, et al.
Human Molecular Genetics|July 29, 2016
An inactivating mutation in intestinal cell kinase, ICK, impairs hedgehog signalling and causes short rib-polydactyly syndromeS Paige Taylor, Michaela Kunova Bosakova, Miroslav Varecha, et al.
EMBO Molecular Medicine|November 17, 2020
Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signalingMichaela Bosakova, Sara P Abraham, Alexandru Nita, et al.
Nature Communications|June 6, 2015
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transportMiriam Schmidts, Yuqing Hou, Claudio R Cortés, et al.
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