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Proceedings of the National Academy of Sciences of the United States of America|August 5, 2010
MTM1 mutation associated with X-linked myotubular myopathy in Labrador RetrieversAlan H Beggs, Johann Böhm, Elizabeth Snead, et al.
Genome Biology|October 11, 2019
Correction to: African evolutionary history inferred from whole genome sequence data of 44 indigenous African populationsShaohua Fan, Derek E Kelly, Marcia H Beltrame, et al.
Science Translational Medicine|May 22, 2020
AMELIE speeds Mendelian diagnosis by matching patient phenotype and genotype to primary literatureJohannes Birgmeier, Maximilian Haeussler, Cole A Deisseroth, et al.
South African Journal of Sports Medicine|November 5, 2024
End-to-end SARS-CoV-2 transmission risks in sport: Current evidence and practical recommendationsB Jones, G Phillips, F Valeriani, et al.
The Science of the Total Environment|March 27, 2018
Dynamic ecological observations from satellites inform aerobiology of allergenic grass pollenRakhesh Devadas, Alfredo R Huete, Don Vicendese, et al.
Annals of Neurology|January 24, 2020
Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French CanadiansDavid Pellerin, Asli Aykanat, Benjamin Ellezam, et al.
The Journal of Clinical Investigation|March 10, 2020
Claudin-2 deficiency associates with hypercalciuria in mice and human kidney stone diseaseJoshua N Curry, Matthew Saurette, Masomeh Askari, et al.
American Journal of Human Genetics|August 5, 2014
SPEG interacts with myotubularin, and its deficiency causes centronuclear myopathy with dilated cardiomyopathyPankaj B Agrawal, Christopher R Pierson, Mugdha Joshi, et al.
Public Health|January 17, 2022
Investigating the association between COVID-19 vaccination and care home outbreak frequency and durationD T Bradley, S Murphy, P McWilliams, et al.
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