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Alanna Strong

Showing results (21-30 of 69) with videos related to

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Clinical Dysmorphology|June 21, 2021
X-Autosome translocations: X-inactivation and effect on phenotypeAlanna Strong, Katharine Press Callahan, Rose Guo, et al.
Cureus|February 22, 2024
An Adolescent Boy With Hypoxia, Microscopic Hematuria, and HypertensionMelissa S Zhou, Clement D Lee, Benjamin J Lerman, et al.
Annals of Neurology|July 22, 2014
Targeted treatment of migrating partial seizures of infancy with quinidineDavid Bearden, Alanna Strong, Jessica Ehnot, et al.
Seminars in Ophthalmology|April 22, 2024
Punctal Atresia As a Clinical Indicator of Systemic Genetic AnomaliesDaphna Landau-Prat, Rayna Marshall, Alanna Strong, et al.
Ophthalmic Plastic and Reconstructive Surgery|December 26, 2024
Ocular and Systemic Abnormalities in Punctal AgenesisRayna F Marshall, Daphna Landau-Prat, Alanna Strong, et al.
Journal of Crohn'S & Colitis|February 17, 2025
The ulcerative colitis risk gene adenylyl cyclase 7 restrains the T-helper 2 phenotype and Class II antigen presentationChristopher J Cardinale, Yichuan Liu, Aayush Kevadia, et al.
Clinical & Experimental Ophthalmology|April 21, 2021
"Blepharophimosis-plus" syndromes: Frequency of systemic genetic disorders that also include blepharophimosisDaphna Landau Prat, Brian J Nguyen, Alanna Strong, et al.
Molecular Genetics and Metabolism|August 19, 2023
Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentationXinying Hong, Andrew C Edmondson, Alanna Strong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2022
The current state of adult metabolic medicine in the United States: Results of a nationwide surveyJessica I Gold, Nina B Gold, Alanna Strong, et al.
American Journal of Medical Genetics. Part A|December 10, 2023
Patent ductus arteriosus and coarctation of the aorta in association with PRDM6 variantsHelen M Stanley, Brian R White, Christopher J LaRosa, et al.
Pageof 7

Showing results (21-30 of 69) with videos related to

Sort By:
Pageof 7
Clinical Dysmorphology|June 21, 2021
X-Autosome translocations: X-inactivation and effect on phenotypeAlanna Strong, Katharine Press Callahan, Rose Guo, et al.
Cureus|February 22, 2024
An Adolescent Boy With Hypoxia, Microscopic Hematuria, and HypertensionMelissa S Zhou, Clement D Lee, Benjamin J Lerman, et al.
Annals of Neurology|July 22, 2014
Targeted treatment of migrating partial seizures of infancy with quinidineDavid Bearden, Alanna Strong, Jessica Ehnot, et al.
Seminars in Ophthalmology|April 22, 2024
Punctal Atresia As a Clinical Indicator of Systemic Genetic AnomaliesDaphna Landau-Prat, Rayna Marshall, Alanna Strong, et al.
Ophthalmic Plastic and Reconstructive Surgery|December 26, 2024
Ocular and Systemic Abnormalities in Punctal AgenesisRayna F Marshall, Daphna Landau-Prat, Alanna Strong, et al.
Journal of Crohn'S & Colitis|February 17, 2025
The ulcerative colitis risk gene adenylyl cyclase 7 restrains the T-helper 2 phenotype and Class II antigen presentationChristopher J Cardinale, Yichuan Liu, Aayush Kevadia, et al.
Clinical & Experimental Ophthalmology|April 21, 2021
"Blepharophimosis-plus" syndromes: Frequency of systemic genetic disorders that also include blepharophimosisDaphna Landau Prat, Brian J Nguyen, Alanna Strong, et al.
Molecular Genetics and Metabolism|August 19, 2023
Combined PMM2-CDG and hereditary fructose intolerance in a patient with mild clinical presentationXinying Hong, Andrew C Edmondson, Alanna Strong, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 11, 2022
The current state of adult metabolic medicine in the United States: Results of a nationwide surveyJessica I Gold, Nina B Gold, Alanna Strong, et al.
American Journal of Medical Genetics. Part A|December 10, 2023
Patent ductus arteriosus and coarctation of the aorta in association with PRDM6 variantsHelen M Stanley, Brian R White, Christopher J LaRosa, et al.
Pageof 7