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Morgan Newman

Showing results (41-50 of 46) with videos related to

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Journal of Lower Genital Tract Disease|January 10, 2025
Applying Results of Extended Genotyping to Management of Positive Cervicovaginal Human Papillomavirus Test Results: Enduring GuidelinesL Stewart Massad, Megan A Clarke, Rebecca B Perkins, et al.
Journal of Alzheimer'S Disease : JAD|March 15, 2021
Relevance of a Truncated PRESENILIN 2 Transcript to Alzheimer's Disease and NeurodegenerationSeyyed Hani Moussavi Nik, Tenielle Porter, Morgan Newman, et al.
NPJ Genomic Medicine|December 20, 2018
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
NPJ Genomic Medicine|June 25, 2019
Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Annals of Clinical and Translational Neurology|April 26, 2019
Alternative splicing in a presenilin 2 variant associated with Alzheimer diseaseJacquelyn E Braggin, Stephanie A Bucks, Meredith M Course, et al.
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Showing results (41-50 of 46) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 46 results.
Journal of Lower Genital Tract Disease|January 10, 2025
Applying Results of Extended Genotyping to Management of Positive Cervicovaginal Human Papillomavirus Test Results: Enduring GuidelinesL Stewart Massad, Megan A Clarke, Rebecca B Perkins, et al.
Journal of Alzheimer'S Disease : JAD|March 15, 2021
Relevance of a Truncated PRESENILIN 2 Transcript to Alzheimer's Disease and NeurodegenerationSeyyed Hani Moussavi Nik, Tenielle Porter, Morgan Newman, et al.
NPJ Genomic Medicine|December 20, 2018
Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
NPJ Genomic Medicine|June 25, 2019
Erratum: Author Correction: Pathogenic copy number variants that affect gene expression contribute to genomic burden in cerebral palsyMark A Corbett, Clare L van Eyk, Dani L Webber, et al.
Genes|August 26, 2023
Aicardi Syndrome Is a Genetically Heterogeneous DisorderThuong T Ha, Rosemary Burgess, Morgan Newman, et al.
Annals of Clinical and Translational Neurology|April 26, 2019
Alternative splicing in a presenilin 2 variant associated with Alzheimer diseaseJacquelyn E Braggin, Stephanie A Bucks, Meredith M Course, et al.
Pageof 5