Showing results (131-140 of 138) with videos related to
Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 138 results.
JBI Database of Systematic Reviews and Implementation Reports|January 12, 2018
Nurse experiences of medication administration to people with swallowing difficulties living in aged care facilities: a systematic review of qualitative evidenceAida Sefidani Forough, Simon Y M Wong, Esther T L Lau, et al.Hereditary Cancer in Clinical Practice|January 27, 2018
Genetic variants of prospectively demonstrated phenocopies in <i>BRCA1/2</i> kindredsMev Dominguez-Valentin, D Gareth R Evans, Sigve Nakken, et al.Animal : an International Journal of Animal Bioscience|March 24, 2012
Advances in research on the prenatal development of skeletal muscle in animals in relation to the quality of muscle-based food. I. Regulation of myogenesis and environmental impactC Rehfeldt, M F W Te Pas, K Wimmers, et al.Proceedings of the National Academy of Sciences of the United States of America|October 5, 2007
Transcription factor expression in lipopolysaccharide-activated peripheral-blood-derived mononuclear cellsJared C Roach, Kelly D Smith, Katie L Strobe, et al.Animal : an International Journal of Animal Bioscience|March 24, 2012
Advances in research on the prenatal development of skeletal muscle in animals in relation to the quality of muscle-based food. II--Genetic factors related to animal performance and advances in methodologyC Rehfeldt, M F W Te Pas, K Wimmers, et al.Scientific Reports|December 8, 2019
Results of multigene panel testing in familial cancer cases without genetic cause demonstrated by single gene testingMev Dominguez-Valentin, Sigve Nakken, Hélène Tubeuf, et al.Development (Cambridge, England)|October 25, 2002
A zebrafish sox9 gene required for cartilage morphogenesisYi-Lin Yan, Craig T Miller, Robert M Nissen, et al.Journal of Medical Genetics|February 5, 2016
Mutations in EXOSC2 are associated with a novel syndrome characterised by retinitis pigmentosa, progressive hearing loss, premature ageing, short stature, mild intellectual disability and distinctive gestaltNataliya Di Donato, Teresa Neuhann, Anne-Karin Kahlert, et al.Pageof 14