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Megan F Baxter

Showing results (1-10 of 7) with videos related to

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International Journal of Molecular Sciences|September 14, 2024
Gene Therapy for AchromatopsiaMegan F Baxter, Grace A Borchert
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, et al.
Antibiotics (Basel, Switzerland)|August 6, 2021
Antimicrobial Prescribing in the Emergency Department; Who Is Calling the Shots?Laura M Hamill, Julia Bonnett, Megan F Baxter, et al.
Progress in Retinal and Eye Research|April 5, 2026
Ophthalmic manifestations of mitochondrial disordersMegan F Baxter, Grace A Borchert, Emma L Blakely, et al.
American Journal of Medical Genetics. Part A|June 6, 2026
On the Path to Pediatric Genetics: Reflections From Future CliniciansClaire M Kittock, Rachel H Ceron, Kochakorn Buasri, et al.
American Journal of Human Genetics|March 3, 2018
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2Petra Lassuthova, Adriana P Rebelo, Gianina Ravenscroft, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
International Journal of Molecular Sciences|September 14, 2024
Gene Therapy for AchromatopsiaMegan F Baxter, Grace A Borchert
Frontiers in Pediatrics|November 29, 2023
Surfacing undiagnosed disease: consideration, counting and codingMegan F Baxter, Michele Hansen, Dylan Gration, et al.
Antibiotics (Basel, Switzerland)|August 6, 2021
Antimicrobial Prescribing in the Emergency Department; Who Is Calling the Shots?Laura M Hamill, Julia Bonnett, Megan F Baxter, et al.
Progress in Retinal and Eye Research|April 5, 2026
Ophthalmic manifestations of mitochondrial disordersMegan F Baxter, Grace A Borchert, Emma L Blakely, et al.
American Journal of Medical Genetics. Part A|June 6, 2026
On the Path to Pediatric Genetics: Reflections From Future CliniciansClaire M Kittock, Rachel H Ceron, Kochakorn Buasri, et al.
American Journal of Human Genetics|March 3, 2018
Mutations in ATP1A1 Cause Dominant Charcot-Marie-Tooth Type 2Petra Lassuthova, Adriana P Rebelo, Gianina Ravenscroft, et al.
Medrxiv : the Preprint Server for Health Sciences|March 11, 2026
Clinical, <i>in vitro,</i> and <i>in vivo</i> evidence of <i>WAPL</i> as a novel cohesinopathy gene and phenotypic driver of 10q22.3q23.2 genomic disorderPhilip M Boone, Serkan Erdin, Abucar Mohamed, et al.
Pageof 1