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Michael H Duyzend

Showing results (1-10 of 17) with videos related to

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The Journal of Pediatrics|March 28, 2022
50 Years Ago in TheJournalofPediatrics: Billions of Genomes: Mosaicism in Turner SyndromeMichael H Duyzend
The Journal of Pediatrics|October 27, 2021
50 Years Ago in TheJournalofPediatrics: Logic of Biochemical Discovery in Pompe DiseaseMichael H Duyzend
Biological Psychiatry|April 7, 2015
Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism"Michael H Duyzend, Evan E Eichler
Molecular Systems Biology|December 8, 2011
Non-DNA-binding cofactors enhance DNA-binding specificity of a transcriptional regulatory complexTrevor Siggers, Michael H Duyzend, Jessica Reddy, et al.
American Journal of Human Genetics|January 11, 2016
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNVMichael H Duyzend, Xander Nuttle, Bradley P Coe, et al.
American Journal of Human Genetics|March 4, 2014
A higher mutational burden in females supports a "female protective model" in neurodevelopmental disordersSébastien Jacquemont, Bradley P Coe, Micha Hersch, et al.
Prenatal Diagnosis|January 19, 2024
Improving prenatal diagnosis through standards and aggregationMichael H Duyzend, Pilar Cacheiro, Julius O B Jacobsen, et al.
Clinical Case Reports|January 30, 2018
Longitudinal report of child with de novo 16p11.2 triplicationArianne S Wallace, Caitlin M Hudac, Kyle J Steinman, et al.
Genome Biology|March 11, 2017
The birth of a human-specific neural gene by incomplete duplication and gene fusionMax L Dougherty, Xander Nuttle, Osnat Penn, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|November 17, 2011
Synthesis and evaluation of substrate analogue inhibitors of trypanothione reductaseMichael H Duyzend, Christopher T Clark, Shayna L Simmons, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
The Journal of Pediatrics|March 28, 2022
50 Years Ago in TheJournalofPediatrics: Billions of Genomes: Mosaicism in Turner SyndromeMichael H Duyzend
The Journal of Pediatrics|October 27, 2021
50 Years Ago in TheJournalofPediatrics: Logic of Biochemical Discovery in Pompe DiseaseMichael H Duyzend
Biological Psychiatry|April 7, 2015
Genotype-first analysis of the 16p11.2 deletion defines a new type of "autism"Michael H Duyzend, Evan E Eichler
Molecular Systems Biology|December 8, 2011
Non-DNA-binding cofactors enhance DNA-binding specificity of a transcriptional regulatory complexTrevor Siggers, Michael H Duyzend, Jessica Reddy, et al.
American Journal of Human Genetics|January 11, 2016
Maternal Modifiers and Parent-of-Origin Bias of the Autism-Associated 16p11.2 CNVMichael H Duyzend, Xander Nuttle, Bradley P Coe, et al.
American Journal of Human Genetics|March 4, 2014
A higher mutational burden in females supports a "female protective model" in neurodevelopmental disordersSébastien Jacquemont, Bradley P Coe, Micha Hersch, et al.
Prenatal Diagnosis|January 19, 2024
Improving prenatal diagnosis through standards and aggregationMichael H Duyzend, Pilar Cacheiro, Julius O B Jacobsen, et al.
Clinical Case Reports|January 30, 2018
Longitudinal report of child with de novo 16p11.2 triplicationArianne S Wallace, Caitlin M Hudac, Kyle J Steinman, et al.
Genome Biology|March 11, 2017
The birth of a human-specific neural gene by incomplete duplication and gene fusionMax L Dougherty, Xander Nuttle, Osnat Penn, et al.
Journal of Enzyme Inhibition and Medicinal Chemistry|November 17, 2011
Synthesis and evaluation of substrate analogue inhibitors of trypanothione reductaseMichael H Duyzend, Christopher T Clark, Shayna L Simmons, et al.
Pageof 2