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The Journal of Pediatrics
|
March 28, 2022
50 Years Ago in TheJournalofPediatrics: Billions of Genomes: Mosaicism in Turner Syndrome
Michael H Duyzend
The Journal of Pediatrics
|
October 27, 2021
50 Years Ago in TheJournalofPediatrics: Logic of Biochemical Discovery in Pompe Disease
Michael 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 complex
Trevor 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 CNV
Michael 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 disorders
Sébastien Jacquemont, Bradley P Coe, Micha Hersch, et al.
Prenatal Diagnosis
|
January 19, 2024
Improving prenatal diagnosis through standards and aggregation
Michael 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 triplication
Arianne 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 fusion
Max 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 reductase
Michael H Duyzend, Christopher T Clark, Shayna L Simmons, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
The Journal of Pediatrics
|
March 28, 2022
50 Years Ago in TheJournalofPediatrics: Billions of Genomes: Mosaicism in Turner Syndrome
Michael H Duyzend
The Journal of Pediatrics
|
October 27, 2021
50 Years Ago in TheJournalofPediatrics: Logic of Biochemical Discovery in Pompe Disease
Michael 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 complex
Trevor 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 CNV
Michael 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 disorders
Sébastien Jacquemont, Bradley P Coe, Micha Hersch, et al.
Prenatal Diagnosis
|
January 19, 2024
Improving prenatal diagnosis through standards and aggregation
Michael 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 triplication
Arianne 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 fusion
Max 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 reductase
Michael H Duyzend, Christopher T Clark, Shayna L Simmons, et al.
Page
of 2