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Showing results (721-730 of 729) with videos related to

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American Journal of Human Genetics|November 8, 2018
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal NeuropathyKatharina Danhauser, Bader Alhaddad, Christine Makowski, et al.
The Journal of Allergy and Clinical Immunology. Global|September 29, 2023
The SunBEAm birth cohort: Protocol designCorinne Keet, Scott H Sicherer, Supinda Bunyavanich, et al.
Human Mutation|April 26, 2019
Mutation update for the SATB2 geneYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.
Frontiers in Neurology|February 17, 2022
Fluid and Tissue Biomarkers of Lewy Body Dementia: Report of an LBDA SymposiumGregory D Scott, Moriah R Arnold, Thomas G Beach, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Nature Communications|October 2, 2020
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disordersTianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|September 7, 2020
The fingerprint of the summer 2018 drought in Europe on ground-based atmospheric CO<sub>2</sub> measurementsM Ramonet, P Ciais, F Apadula, et al.
Nature Communications|October 22, 2020
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disordersTianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
The New England Journal of Medicine|June 17, 2026
Cefazolin for Methicillin-Susceptible <i>Staphylococcus aureus</i> Bacteremia, Todd C Lee, Lauren A Barina, et al.
Pageof 73

Showing results (721-730 of 729) with videos related to

Sort By:
Pageof 73
You have reached the last page of results.This site can display upto 729 results.
American Journal of Human Genetics|November 8, 2018
Bi-allelic ADPRHL2 Mutations Cause Neurodegeneration with Developmental Delay, Ataxia, and Axonal NeuropathyKatharina Danhauser, Bader Alhaddad, Christine Makowski, et al.
The Journal of Allergy and Clinical Immunology. Global|September 29, 2023
The SunBEAm birth cohort: Protocol designCorinne Keet, Scott H Sicherer, Supinda Bunyavanich, et al.
Human Mutation|April 26, 2019
Mutation update for the SATB2 geneYuri A Zarate, Katherine A Bosanko, Aisling R Caffrey, et al.
Frontiers in Neurology|February 17, 2022
Fluid and Tissue Biomarkers of Lewy Body Dementia: Report of an LBDA SymposiumGregory D Scott, Moriah R Arnold, Thomas G Beach, et al.
Journal of Medical Genetics|July 17, 2008
Clinical and molecular delineation of the 17q21.31 microdeletion syndromeD A Koolen, A J Sharp, J A Hurst, et al.
Nature Communications|October 2, 2020
Large-scale targeted sequencing identifies risk genes for neurodevelopmental disordersTianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|September 7, 2020
The fingerprint of the summer 2018 drought in Europe on ground-based atmospheric CO<sub>2</sub> measurementsM Ramonet, P Ciais, F Apadula, et al.
Nature Communications|October 22, 2020
Author Correction: Large-scale targeted sequencing identifies risk genes for neurodevelopmental disordersTianyun Wang, Kendra Hoekzema, Davide Vecchio, et al.
The New England Journal of Medicine|June 17, 2026
Cefazolin for Methicillin-Susceptible <i>Staphylococcus aureus</i> Bacteremia, Todd C Lee, Lauren A Barina, et al.
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