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J Curry

Showing results (611-620 of 644) with videos related to

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JAMA|March 8, 2017
Screening for Gynecologic Conditions With Pelvic Examination: US Preventive Services Task Force Recommendation Statement, Kirsten Bibbins-Domingo, David C Grossman, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 25, 2019
Biodegradable nanofiber-based piezoelectric transducerEli J Curry, Thinh T Le, Ritopa Das, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
American Journal of Human Genetics|September 29, 2021
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomaliesGabrielle Lemire, Yoko A Ito, Aren E Marshall, et al.
Neurosurgery|January 13, 2023
Epilepsy Surgery in Young Children With Tuberous Sclerosis Complex: A Novel Hybrid Multimodal Surgical ApproachVijay M Ravindra, Patrick J Karas, Tyler T Lazaro, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 10, 2026
Prompt-directed ambient artificial intelligence for automated multidisciplinary tumor board documentationR Philips, A Mahajan, L Estephan, et al.
Frontiers in Molecular Neuroscience|March 3, 2020
Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export FactorRaman Kumar, Elizabeth Palmer, Alison E Gardner, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical regionEugen-Matthias Strehle, Linbo Yu, Jill A Rosenfeld, et al.
American Journal of Human Genetics|May 31, 2016
A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones SyndromeStephen R F Twigg, Robert B Hufnagel, Kerry A Miller, et al.
Nature Genetics|October 2, 2012
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysmAlexander J Doyle, Jefferson J Doyle, Seneca L Bessling, et al.
Pageof 65

Showing results (611-620 of 644) with videos related to

Sort By:
Pageof 65
JAMA|March 8, 2017
Screening for Gynecologic Conditions With Pelvic Examination: US Preventive Services Task Force Recommendation Statement, Kirsten Bibbins-Domingo, David C Grossman, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 25, 2019
Biodegradable nanofiber-based piezoelectric transducerEli J Curry, Thinh T Le, Ritopa Das, et al.
Clinical Genetics|December 31, 2020
Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2Yuri A Zarate, Katherine A Bosanko, Mary Ann Thomas, et al.
American Journal of Human Genetics|September 29, 2021
ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomaliesGabrielle Lemire, Yoko A Ito, Aren E Marshall, et al.
Neurosurgery|January 13, 2023
Epilepsy Surgery in Young Children With Tuberous Sclerosis Complex: A Novel Hybrid Multimodal Surgical ApproachVijay M Ravindra, Patrick J Karas, Tyler T Lazaro, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|June 10, 2026
Prompt-directed ambient artificial intelligence for automated multidisciplinary tumor board documentationR Philips, A Mahajan, L Estephan, et al.
Frontiers in Molecular Neuroscience|March 3, 2020
Expanding Clinical Presentations Due to Variations in THOC2 mRNA Nuclear Export FactorRaman Kumar, Elizabeth Palmer, Alison E Gardner, et al.
American Journal of Medical Genetics. Part A|August 1, 2012
Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical regionEugen-Matthias Strehle, Linbo Yu, Jill A Rosenfeld, et al.
American Journal of Human Genetics|May 31, 2016
A Recurrent Mosaic Mutation in SMO, Encoding the Hedgehog Signal Transducer Smoothened, Is the Major Cause of Curry-Jones SyndromeStephen R F Twigg, Robert B Hufnagel, Kerry A Miller, et al.
Nature Genetics|October 2, 2012
Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysmAlexander J Doyle, Jefferson J Doyle, Seneca L Bessling, et al.
Pageof 65