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Showing results (1121-1130 of 1,127) with videos related to

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Nature|October 12, 2018
The dispersion-brightness relation for fast radio bursts from a wide-field surveyR M Shannon, J-P Macquart, K W Bannister, et al.
Journal of Medical Genetics|December 4, 2009
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individualsBenjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, et al.
American Journal of Human Genetics|December 4, 2018
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2025
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorderAmber S E van Oirsouw, Pavla Nedbalova, Miroslava Hancarova, et al.
Preventive Medicine Reports|March 22, 2022
COVID-19 stressors and health behaviors: A multilevel longitudinal study across 86 countriesShian-Ling Keng, Michael V Stanton, LeeAnn B Haskins, et al.
Global Ecology and Biogeography : a Journal of Macroecology|August 28, 2018
BioTIME: A database of biodiversity time series for the AnthropoceneMaria Dornelas, Laura H Antão, Faye Moyes, et al.
Pageof 113

Showing results (1121-1130 of 1,127) with videos related to

Sort By:
Pageof 113
You have reached the last page of results.This site can display upto 1,127 results.
Nature|October 12, 2018
The dispersion-brightness relation for fast radio bursts from a wide-field surveyR M Shannon, J-P Macquart, K W Bannister, et al.
Journal of Medical Genetics|December 4, 2009
Mutations in ZIC2 in human holoprosencephaly: description of a novel ZIC2 specific phenotype and comprehensive analysis of 157 individualsBenjamin D Solomon, Felicitas Lacbawan, Sandra Mercier, et al.
American Journal of Human Genetics|December 4, 2018
DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable ImmunodeficiencyClare V Logan, Jennie E Murray, David A Parry, et al.
The Journal of Clinical Endocrinology and Metabolism|December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiencyNils Krone, Nicole Reisch, Jan Idkowiak, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 17, 2025
Pathogenic XPO1 variants cause a dominant neurodevelopmental disorderAmber S E van Oirsouw, Pavla Nedbalova, Miroslava Hancarova, et al.
Preventive Medicine Reports|March 22, 2022
COVID-19 stressors and health behaviors: A multilevel longitudinal study across 86 countriesShian-Ling Keng, Michael V Stanton, LeeAnn B Haskins, et al.
Global Ecology and Biogeography : a Journal of Macroecology|August 28, 2018
BioTIME: A database of biodiversity time series for the AnthropoceneMaria Dornelas, Laura H Antão, Faye Moyes, et al.
Pageof 113