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ABOUT JoVE

Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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Testimonials Subscriptions Access Resources Library Advisory Board FAQ

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JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

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John J Alexander

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Genetics & Epigenetics|October 30, 2015

Csf2 and Ptgs2 Epigenetic Dysregulation in Diabetes-prone Bicongenic B6.NODC11bxC1tb MiceErin Garrigan, Nicole S Belkin, Federica Seydel, et al.

JAMA Pediatrics|August 1, 2017

Early-Life Epilepsies and the Emerging Role of Genetic TestingAnne T Berg, Jason Coryell, Russell P Saneto, et al.

Molecular Therapy : the Journal of the American Society of Gene Therapy|June 2, 2017

Optimization of Retinal Gene Therapy for X-Linked Retinitis Pigmentosa Due to RPGR MutationsWilliam A Beltran, Artur V Cideciyan, Shannon E Boye, et al.

Pediatric Neurology|May 25, 2020

Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated SyndromeHannah Lewis, Debopam Samanta, Jenny-Li Örsell, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2019

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert PanelJun Shen, Andrea M Oza, Ignacio Del Castillo, et al.

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Search research articles

Showing results (31-40 of 35) with videos related to

Sort By:

Pageof 4

You have reached the last page of results.This site can display upto 35 results.

Genetics & Epigenetics|October 30, 2015

Csf2 and Ptgs2 Epigenetic Dysregulation in Diabetes-prone Bicongenic B6.NODC11bxC1tb MiceErin Garrigan, Nicole S Belkin, Federica Seydel, et al.

JAMA Pediatrics|August 1, 2017

Early-Life Epilepsies and the Emerging Role of Genetic TestingAnne T Berg, Jason Coryell, Russell P Saneto, et al.

Molecular Therapy : the Journal of the American Society of Gene Therapy|June 2, 2017

Optimization of Retinal Gene Therapy for X-Linked Retinitis Pigmentosa Due to RPGR MutationsWilliam A Beltran, Artur V Cideciyan, Shannon E Boye, et al.

Pediatric Neurology|May 25, 2020

Epilepsy and Electroencephalographic Abnormalities in SATB2-Associated SyndromeHannah Lewis, Debopam Samanta, Jenny-Li Örsell, et al.

Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 5, 2019

Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert PanelJun Shen, Andrea M Oza, Ignacio Del Castillo, et al.

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