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Christopher Lau

Showing results (271-280 of 284) with videos related to

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American Journal of Human Genetics|September 7, 2019
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar HypoplasiaOguz Kanca, Jonathan C Andrews, Pei-Tseng Lee, et al.
American Journal of Human Genetics|July 23, 2019
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar HypoplasiaOguz Kanca, Jonathan C Andrews, Pei-Tseng Lee, et al.
American Journal of Human Genetics|November 8, 2018
Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental DelayMarie Morimoto, Helen Waller-Evans, Zineb Ammous, et al.
Neuron|June 24, 2014
A high-resolution spatiotemporal atlas of gene expression of the developing mouse brainCarol L Thompson, Lydia Ng, Vilas Menon, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|December 5, 2022
Editor's Choice - Infective Native Aortic Aneurysms: A Delphi Consensus Document on Terminology, Definition, Classification, Diagnosis, and Reporting StandardsKarl Sörelius, Thomas R Wyss, , et al.
Brain : a Journal of Neurology|October 1, 2022
Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndromeAriane Soldatos, Thomas B Nutman, Tory Johnson, et al.
The Journal of Comparative Neurology|December 6, 2016
Comprehensive cellular-resolution atlas of the adult human brainSong-Lin Ding, Joshua J Royall, Susan M Sunkin, et al.
The Journal of Comparative Neurology|July 16, 2016
Comprehensive cellular-resolution atlas of the adult human brainSong-Lin Ding, Joshua J Royall, Susan M Sunkin, et al.
American Journal of Human Genetics|August 6, 2024
Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorderMarie Morimoto, Eunjin Ryu, Benjamin J Steger, et al.
Nature Genetics|July 6, 2010
Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapyJordi Barretina, Barry S Taylor, Shantanu Banerji, et al.
Pageof 29

Showing results (271-280 of 284) with videos related to

Sort By:
Pageof 29
American Journal of Human Genetics|September 7, 2019
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar HypoplasiaOguz Kanca, Jonathan C Andrews, Pei-Tseng Lee, et al.
American Journal of Human Genetics|July 23, 2019
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar HypoplasiaOguz Kanca, Jonathan C Andrews, Pei-Tseng Lee, et al.
American Journal of Human Genetics|November 8, 2018
Bi-allelic CCDC47 Variants Cause a Disorder Characterized by Woolly Hair, Liver Dysfunction, Dysmorphic Features, and Global Developmental DelayMarie Morimoto, Helen Waller-Evans, Zineb Ammous, et al.
Neuron|June 24, 2014
A high-resolution spatiotemporal atlas of gene expression of the developing mouse brainCarol L Thompson, Lydia Ng, Vilas Menon, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|December 5, 2022
Editor's Choice - Infective Native Aortic Aneurysms: A Delphi Consensus Document on Terminology, Definition, Classification, Diagnosis, and Reporting StandardsKarl Sörelius, Thomas R Wyss, , et al.
Brain : a Journal of Neurology|October 1, 2022
Genomic analysis, immunomodulation and deep phenotyping of patients with nodding syndromeAriane Soldatos, Thomas B Nutman, Tory Johnson, et al.
The Journal of Comparative Neurology|December 6, 2016
Comprehensive cellular-resolution atlas of the adult human brainSong-Lin Ding, Joshua J Royall, Susan M Sunkin, et al.
The Journal of Comparative Neurology|July 16, 2016
Comprehensive cellular-resolution atlas of the adult human brainSong-Lin Ding, Joshua J Royall, Susan M Sunkin, et al.
American Journal of Human Genetics|August 6, 2024
Expanding the genetic and phenotypic landscape of replication factor C complex-related disorders: RFC4 deficiency is linked to a multisystemic disorderMarie Morimoto, Eunjin Ryu, Benjamin J Steger, et al.
Nature Genetics|July 6, 2010
Subtype-specific genomic alterations define new targets for soft-tissue sarcoma therapyJordi Barretina, Barry S Taylor, Shantanu Banerji, et al.
Pageof 29