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American Journal of Medical Genetics. Part A|April 24, 2023
U2AF2 variant in a patient with developmental delay, dysmorphic features, and epilepsyClaire M Kittock, Mohamad Saifeddine, Lisa Straight, et al.
Developmental Neurobiology|March 2, 2023
Advances in in utero electroporationClaire M Kittock, Louis-Jan Pilaz
South Dakota Medicine : the Journal of the South Dakota State Medical Association|July 29, 2026
Community Engaged Medical Education: Give Kids the WorldMegan M Jorgensen, Claire M Kittock, Alison Gisi, et al.
HGG Advances|August 25, 2025
Modeling MPPH syndrome in vivo using Breasi-CRISPRClaire M Kittock, Krishna Karia, Pratiksha Kc, et al.
Development (Cambridge, England)|August 22, 2022
Breasi-CRISPR: an efficient genome-editing method to interrogate protein localization and protein-protein interactions in the embryonic mouse cortexBrandon L Meyerink, Pratiksha Kc, Neeraj K Tiwari, et al.
HGG Advances|November 1, 2024
RLIM-specific activity reporters define variant pathogenicity in Tonne-Kalscheuer syndromeVenkateshwarlu Bandi, Martin Rennie, Intisar Koch, et al.
Neonatology|May 18, 2021
Diamond-Blackfan Anemia: A Case Report and Review of the LiteratureKaitlyn M Dorn, Kaitlyn D Burns, Maija A R Trout, et al.
Communications Biology|September 19, 2019
Development of R7BP inhibitors through cross-linking coupled mass spectrometry and integrated modelingPoorni R Adikaram, Jian-Hua Zhang, Claire M Kittock, et al.
Neurology. Clinical Practice|April 12, 2021
Disparities in Access to Neurologic Telemedicine During the COVID-19 Pandemic: A Bronx TaleJonathan M Gursky, Alex Boro, Sheri Escalante, et al.
Epilepsia|December 21, 2024
Rare dysfunctional SCN2A variants are associated with malformation of cortical developmentJérôme Clatot, Christopher H Thompson, Susan Sotardi, et al.
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