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Raymond Dalgleish

Showing results (41-50 of 47) with videos related to

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Histopathology|March 19, 2026
The WHO Classification of Genetic Tumour Syndromes: Considerations for histopathologyIan A Cree, Mark J Arends, Joseph D Khoury, et al.
Human Mutation|November 30, 2020
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journalsJan Higgins, Raymond Dalgleish, Johan T den Dunnen, et al.
Clinical Genetics|June 17, 2026
The WHO Classification of Genetic Tumour Syndromes: Considerations for GeneticsIan A Cree, Mark J Arends, Joseph D Khoury, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discoveryDaniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
HGG Advances|October 12, 2024
A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discoveryDaniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
Human Mutation|March 24, 2009
Planning the human variome project: the Spain reportJim Kaput, Richard G H Cotton, Lauren Hardman, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
Histopathology|March 19, 2026
The WHO Classification of Genetic Tumour Syndromes: Considerations for histopathologyIan A Cree, Mark J Arends, Joseph D Khoury, et al.
Human Mutation|November 30, 2020
Verifying nomenclature of DNA variants in submitted manuscripts: Guidance for journalsJan Higgins, Raymond Dalgleish, Johan T den Dunnen, et al.
Clinical Genetics|June 17, 2026
The WHO Classification of Genetic Tumour Syndromes: Considerations for GeneticsIan A Cree, Mark J Arends, Joseph D Khoury, et al.
Human Mutation|November 2, 2006
Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and proteoglycansJoan C Marini, Antonella Forlino, Wayne A Cabral, et al.
Medrxiv : the Preprint Server for Health Sciences|June 10, 2024
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discoveryDaniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
HGG Advances|October 12, 2024
A corpus of GA4GH phenopackets: Case-level phenotyping for genomic diagnostics and discoveryDaniel Danis, Michael J Bamshad, Yasemin Bridges, et al.
Human Mutation|March 24, 2009
Planning the human variome project: the Spain reportJim Kaput, Richard G H Cotton, Lauren Hardman, et al.
Pageof 5