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Showing results (571-580 of 826) with videos related to

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Molecular Psychiatry|March 15, 2017
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disordersP Devanna, X S Chen, J Ho, et al.
Journal of Quantitative Spectroscopy & Radiative Transfer|September 11, 2020
Speed-dependent Voigt lineshape parameter database from dual frequency comb measurements at temperatures up to 1305 K. Part II: Argon-broadened H<sub>2</sub>O absorption, 6801-7188 cm<sup>-1</sup>Jinyu Yang, Paul J Schroeder, Matthew J Cich, et al.
Arthritis Research & Therapy|October 28, 2009
Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathiesNaomi Eidelman, Alan Boyde, Andrew J Bushby, et al.
Stroke|March 14, 2013
Adelaide stroke incidence study: declining stroke rates but many preventable cardioembolic strokesJames M Leyden, Timothy J Kleinig, Jonathan Newbury, et al.
International Journal for Equity in Health|June 18, 2013
Aboriginal Families Study: a population-based study keeping community and policy goals in mind right from the startMary Buckskin, Jackie Ah Kit, Karen Glover, et al.
Journal of Human Genetics|February 4, 2005
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11Kamini Kalidas, Adam C Shaw, Andrew H Crosby, et al.
Journal of Studies on Alcohol and Drugs|June 29, 2019
Prioritization of Outcomes in Efficacy and Effectiveness of Alcohol Brief Intervention Trials: International Multi-Stakeholder e-Delphi Consensus Study to Inform a Core Outcome SetGillian W Shorter, Nick Heather, Jeremy W Bray, et al.
Journal of Medical Genetics|April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patientsH L Archer, J Evans, S Edwards, et al.
Nature Genetics|April 12, 2005
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndromeHans van Bokhoven, Jacopo Celli, Jeroen van Reeuwijk, et al.
Journal of Public Health (Oxford, England)|August 20, 2020
A qualitative account of young people's experiences of alcohol screening and brief interventions in schools: SIPS Jr-HIGH trial findingsE L Giles, G J McGeechan, S J Scott, et al.
Pageof 83

Showing results (571-580 of 826) with videos related to

Sort By:
Pageof 83
Molecular Psychiatry|March 15, 2017
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disordersP Devanna, X S Chen, J Ho, et al.
Journal of Quantitative Spectroscopy & Radiative Transfer|September 11, 2020
Speed-dependent Voigt lineshape parameter database from dual frequency comb measurements at temperatures up to 1305 K. Part II: Argon-broadened H<sub>2</sub>O absorption, 6801-7188 cm<sup>-1</sup>Jinyu Yang, Paul J Schroeder, Matthew J Cich, et al.
Arthritis Research & Therapy|October 28, 2009
Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathiesNaomi Eidelman, Alan Boyde, Andrew J Bushby, et al.
Stroke|March 14, 2013
Adelaide stroke incidence study: declining stroke rates but many preventable cardioembolic strokesJames M Leyden, Timothy J Kleinig, Jonathan Newbury, et al.
International Journal for Equity in Health|June 18, 2013
Aboriginal Families Study: a population-based study keeping community and policy goals in mind right from the startMary Buckskin, Jackie Ah Kit, Karen Glover, et al.
Journal of Human Genetics|February 4, 2005
Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11Kamini Kalidas, Adam C Shaw, Andrew H Crosby, et al.
Journal of Studies on Alcohol and Drugs|June 29, 2019
Prioritization of Outcomes in Efficacy and Effectiveness of Alcohol Brief Intervention Trials: International Multi-Stakeholder e-Delphi Consensus Study to Inform a Core Outcome SetGillian W Shorter, Nick Heather, Jeremy W Bray, et al.
Journal of Medical Genetics|April 14, 2006
CDKL5 mutations cause infantile spasms, early onset seizures, and severe mental retardation in female patientsH L Archer, J Evans, S Edwards, et al.
Nature Genetics|April 12, 2005
MYCN haploinsufficiency is associated with reduced brain size and intestinal atresias in Feingold syndromeHans van Bokhoven, Jacopo Celli, Jeroen van Reeuwijk, et al.
Journal of Public Health (Oxford, England)|August 20, 2020
A qualitative account of young people's experiences of alcohol screening and brief interventions in schools: SIPS Jr-HIGH trial findingsE L Giles, G J McGeechan, S J Scott, et al.
Pageof 83