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R Higgs

Showing results (461-470 of 469) with videos related to

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Biorxiv : the Preprint Server for Biology|April 17, 2023
Interspecies regulatory landscapes and elements revealed by novel joint systematic integration of human and mouse blood cell epigenomesGuanjue Xiang, Xi He, Belinda M Giardine, et al.
Science (New York, N.Y.)|October 18, 2017
Early spectra of the gravitational wave source GW170817: Evolution of a neutron star mergerB J Shappee, J D Simon, M R Drout, et al.
Molecular Psychiatry|April 30, 2020
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndromeJoost Kummeling, Diante E Stremmelaar, Nicholas Raun, et al.
Science (New York, N.Y.)|October 18, 2017
Light curves of the neutron star merger GW170817/SSS17a: Implications for r-process nucleosynthesisM R Drout, A L Piro, B J Shappee, et al.
HGG Advances|November 21, 2022
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorderLot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, et al.
Nature Communications|November 5, 2022
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidyLaura J Grange, John J Reynolds, Farid Ullah, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
American Journal of Human Genetics|February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia PhenotypesLindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Nature Genetics|February 14, 2017
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfismJohn J Reynolds, Louise S Bicknell, Paula Carroll, et al.
Pageof 47

Showing results (461-470 of 469) with videos related to

Sort By:
Pageof 47
You have reached the last page of results.This site can display upto 469 results.
Biorxiv : the Preprint Server for Biology|April 17, 2023
Interspecies regulatory landscapes and elements revealed by novel joint systematic integration of human and mouse blood cell epigenomesGuanjue Xiang, Xi He, Belinda M Giardine, et al.
Science (New York, N.Y.)|October 18, 2017
Early spectra of the gravitational wave source GW170817: Evolution of a neutron star mergerB J Shappee, J D Simon, M R Drout, et al.
Molecular Psychiatry|April 30, 2020
Characterization of SETD1A haploinsufficiency in humans and Drosophila defines a novel neurodevelopmental syndromeJoost Kummeling, Diante E Stremmelaar, Nicholas Raun, et al.
Science (New York, N.Y.)|October 18, 2017
Light curves of the neutron star merger GW170817/SSS17a: Implications for r-process nucleosynthesisM R Drout, A L Piro, B J Shappee, et al.
HGG Advances|November 21, 2022
A clustering of heterozygous missense variants in the crucial chromatin modifier WDR5 defines a new neurodevelopmental disorderLot Snijders Blok, Jolijn Verseput, Dmitrijs Rots, et al.
Nature Communications|November 5, 2022
Pathogenic variants in SLF2 and SMC5 cause segmented chromosomes and mosaic variegated hyperploidyLaura J Grange, John J Reynolds, Farid Ullah, et al.
Nature Genetics|March 23, 2011
Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approachBelinda Giardine, Joseph Borg, Douglas R Higgs, et al.
American Journal of Human Genetics|February 19, 2019
Bi-allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia PhenotypesLindsay C Burrage, John J Reynolds, Nissan Vida Baratang, et al.
Nature Genetics|February 14, 2017
Mutations in DONSON disrupt replication fork stability and cause microcephalic dwarfismJohn J Reynolds, Louise S Bicknell, Paula Carroll, et al.
Pageof 47