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Reena Jethva

Showing results (11-20 of 13) with videos related to

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American Journal of Medical Genetics. Part A|August 5, 2015
A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephalyJaime Imitola, Divya S Khurana, Nadiya M Teplyuk, et al.
Blood|July 26, 2012
Transplanted bone marrow mononuclear cells and MSCs impart clinical benefit to children with osteogenesis imperfecta through different mechanismsSatoru Otsuru, Patricia L Gordon, Kengo Shimono, et al.
Molecular Psychiatry|June 30, 2021
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neuronsKaren Runge, Rémi Mathieu, Stéphane Bugeon, et al.
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Showing results (11-20 of 13) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 13 results.
American Journal of Medical Genetics. Part A|August 5, 2015
A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephalyJaime Imitola, Divya S Khurana, Nadiya M Teplyuk, et al.
Blood|July 26, 2012
Transplanted bone marrow mononuclear cells and MSCs impart clinical benefit to children with osteogenesis imperfecta through different mechanismsSatoru Otsuru, Patricia L Gordon, Kengo Shimono, et al.
Molecular Psychiatry|June 30, 2021
Disruption of NEUROD2 causes a neurodevelopmental syndrome with autistic features via cell-autonomous defects in forebrain glutamatergic neuronsKaren Runge, Rémi Mathieu, Stéphane Bugeon, et al.
Pageof 2