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Melissa MacPherson

Showing results (1-10 of 5) with videos related to

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Journal of the American Medical Informatics Association : JAMIA|October 20, 2007
Identifying smokers with a medical extraction systemCheryl Clark, Kathleen Good, Lesley Jezierny, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 5, 2023
Daniela M Roth, Jeremie Oliver Piña, Melissa MacPherson, et al.
American Journal of Medical Genetics. Part A|November 19, 2022
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinicsApurba Mainali, Taryn Athey, Shalini Bahl, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizuresMichelle Hua, Mohamad-Reza Aghanoori, Melissa MacPherson, et al.
Nature Communications|January 23, 2026
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disordersKevin Uguen, Tiffany Bergot, Marie-Pier Scott-Boyer, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Journal of the American Medical Informatics Association : JAMIA|October 20, 2007
Identifying smokers with a medical extraction systemCheryl Clark, Kathleen Good, Lesley Jezierny, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|June 5, 2023
Daniela M Roth, Jeremie Oliver Piña, Melissa MacPherson, et al.
American Journal of Medical Genetics. Part A|November 19, 2022
Diagnostic yield of clinical exome sequencing in adulthood in medical genetics clinicsApurba Mainali, Taryn Athey, Shalini Bahl, et al.
Medrxiv : the Preprint Server for Health Sciences|July 16, 2025
Genetic variants disrupting activity-dependent CELF2 shuttling cause neuronal hyperexcitability, learning deficits, and seizuresMichelle Hua, Mohamad-Reza Aghanoori, Melissa MacPherson, et al.
Nature Communications|January 23, 2026
De novo variants in the splicing factor gene SF3B1 are associated with neurodevelopmental disordersKevin Uguen, Tiffany Bergot, Marie-Pier Scott-Boyer, et al.
Pageof 1