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Matthew W State

Showing results (41-50 of 123) with videos related to

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American Journal of Medical Genetics. Part A|March 9, 2005
Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23)Carolyn M Drazinic, Adife G Ercan-Sencicek, Laura M Gault, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2005
Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorderArya Mani, Jayaram Radhakrishnan, Anita Farhi, et al.
Neuron|May 30, 2009
Functional and evolutionary insights into human brain development through global transcriptome analysisMatthew B Johnson, Yuka Imamura Kawasawa, Christopher E Mason, et al.
Nature Genetics|April 9, 2008
Rare independent mutations in renal salt handling genes contribute to blood pressure variationWeizhen Ji, Jia Nee Foo, Brian J O'Roak, et al.
Human Mutation|August 7, 2007
Rapid identification of disease-causing mutations using copy number analysis within linkage intervalsFatih Bayrakli, Kaya Bilguvar, Christopher E Mason, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 2, 2009
A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family groupFatih Bayrakli, Ilter Guney, Yasar Bayri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 18, 2012
A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorderKarina Griesi-Oliveira, Danielle de Paula Moreira, Nicole Davis-Wright, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotilityKate E McCluskey, Katherine M Stovell, Karen Law, et al.
Cell|July 2, 2020
A Chromatin Accessibility Atlas of the Developing Human TelencephalonEirene Markenscoff-Papadimitriou, Sean Whalen, Pawel Przytycki, et al.
Nature Communications|March 6, 2025
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotilityKate E McCluskey, Katherine M Stovell, Karen Law, et al.
Pageof 13

Showing results (41-50 of 123) with videos related to

Sort By:
Pageof 13
American Journal of Medical Genetics. Part A|March 9, 2005
Rapid array-based genomic characterization of a subtle structural abnormality: a patient with psychosis and der(18)t(5;18)(p14.1;p11.23)Carolyn M Drazinic, Adife G Ercan-Sencicek, Laura M Gault, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 3, 2005
Syndromic patent ductus arteriosus: evidence for haploinsufficient TFAP2B mutations and identification of a linked sleep disorderArya Mani, Jayaram Radhakrishnan, Anita Farhi, et al.
Neuron|May 30, 2009
Functional and evolutionary insights into human brain development through global transcriptome analysisMatthew B Johnson, Yuka Imamura Kawasawa, Christopher E Mason, et al.
Nature Genetics|April 9, 2008
Rare independent mutations in renal salt handling genes contribute to blood pressure variationWeizhen Ji, Jia Nee Foo, Brian J O'Roak, et al.
Human Mutation|August 7, 2007
Rapid identification of disease-causing mutations using copy number analysis within linkage intervalsFatih Bayrakli, Kaya Bilguvar, Christopher E Mason, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|October 2, 2009
A novel heterozygous deletion within the 3' region of the PAX6 gene causing isolated aniridia in a large family groupFatih Bayrakli, Ilter Guney, Yasar Bayri, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 18, 2012
A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorderKarina Griesi-Oliveira, Danielle de Paula Moreira, Nicole Davis-Wright, et al.
Biorxiv : the Preprint Server for Biology|June 10, 2024
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotilityKate E McCluskey, Katherine M Stovell, Karen Law, et al.
Cell|July 2, 2020
A Chromatin Accessibility Atlas of the Developing Human TelencephalonEirene Markenscoff-Papadimitriou, Sean Whalen, Pawel Przytycki, et al.
Nature Communications|March 6, 2025
Autism gene variants disrupt enteric neuron migration and cause gastrointestinal dysmotilityKate E McCluskey, Katherine M Stovell, Karen Law, et al.
Pageof 13