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American Journal of Human Genetics|November 27, 2012
Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIATobias B Haack, Penelope Hogarth, Michael C Kruer, et al.
BMC Musculoskeletal Disorders|January 7, 2019
Within-person pain variability and physical activity in older adults with osteoarthritis from six European countriesErik J Timmermans, Elisa J de Koning, Natasja M van Schoor, et al.
Brain : a Journal of Neurology|May 21, 2013
β-Propeller protein-associated neurodegeneration: a new X-linked dominant disorder with brain iron accumulationSusan J Hayflick, Michael C Kruer, Allison Gregory, et al.
Journal of the American Geriatrics Society|September 19, 2019
Association Between Osteoarthritis and Social Isolation: Data From the EPOSA StudyPaola Siviero, Nicola Veronese, Toby Smith, et al.
Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
Transplant International : Official Journal of the European Society for Organ Transplantation|November 28, 2025
The Variation in Practice of the Living Donor Kidney Transplant Pathway in the UK: Results of a National SurveyKatie Nightingale, Josh Stephenson, Rajesh Sivaprakasam, et al.
Nature Genetics|October 21, 2003
Positional cloning of a novel gene influencing asthma from chromosome 2q14Maxine Allen, Andrea Heinzmann, Emiko Noguchi, et al.
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