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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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Melissa Jones

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Pediatric Neurology|May 25, 2020

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

American Journal of Human Genetics|July 27, 2021

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in DrosophilaLindsey D Goodman, Heidi Cope, Zelha Nil, et al.

G3 (Bethesda, Md.)|March 6, 2015

Drosophila muller f elements maintain a distinct set of genomic properties over 40 million years of evolutionWilson Leung, Christopher D Shaffer, Laura K Reed, et al.

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Search research articles

Showing results (111-120 of 113) with videos related to

Sort By:

Pageof 12

You have reached the last page of results.This site can display upto 113 results.

Pediatric Neurology|May 25, 2020

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

American Journal of Human Genetics|July 27, 2021

TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in DrosophilaLindsey D Goodman, Heidi Cope, Zelha Nil, et al.

G3 (Bethesda, Md.)|March 6, 2015

Drosophila muller f elements maintain a distinct set of genomic properties over 40 million years of evolutionWilson Leung, Christopher D Shaffer, Laura K Reed, et al.

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