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Vidya Krishnamurthy

Showing results (1-10 of 6) with videos related to

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Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 16, 2007
Automatic recognition of postural allocationsEdward Sazonov, Vidya Krishnamurthy, Oleksandr Makeyev, et al.
Pediatric Radiology|March 8, 2007
Fractures in children with Pompe disease: a potential long-term complicationLaura E Case, Rabi Hanna, Donald P Frush, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephalyYizhou Ye, Megan T Cho, Kyle Retterer, et al.
American Journal of Human Genetics|August 23, 2016
Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in FemalesJennifer M Bain, Megan T Cho, Aida Telegrafi, et al.
American Journal of Human Genetics|July 31, 2020
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA ProcessingAnna Fliedner, Philipp Kirchner, Antje Wiesener, et al.
American Journal of Human Genetics|January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctionJoery den Hoed, Elke de Boer, Norine Voisin, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|November 16, 2007
Automatic recognition of postural allocationsEdward Sazonov, Vidya Krishnamurthy, Oleksandr Makeyev, et al.
Pediatric Radiology|March 8, 2007
Fractures in children with Pompe disease: a potential long-term complicationLaura E Case, Rabi Hanna, Donald P Frush, et al.
Cold Spring Harbor Molecular Case Studies|May 6, 2016
De novo POGZ mutations are associated with neurodevelopmental disorders and microcephalyYizhou Ye, Megan T Cho, Kyle Retterer, et al.
American Journal of Human Genetics|August 23, 2016
Variants in HNRNPH2 on the X Chromosome Are Associated with a Neurodevelopmental Disorder in FemalesJennifer M Bain, Megan T Cho, Aida Telegrafi, et al.
American Journal of Human Genetics|July 31, 2020
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA ProcessingAnna Fliedner, Philipp Kirchner, Antje Wiesener, et al.
American Journal of Human Genetics|January 29, 2021
Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunctionJoery den Hoed, Elke de Boer, Norine Voisin, et al.
Pageof 1