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Emily L Durham

Showing results (31-40 of 36) with videos related to

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Biorxiv : the Preprint Server for Biology|October 3, 2025
TBCK Deficiency Alters Ribosomal Function, RNA Splicing, and miRNA Networks: Insights from Multi-Omics AnalysesAbdias Diaz-Rosado, Kelly Clark, Rajesh Angireddy, et al.
Frontiers in Genetics|June 2, 2022
Meckel's Cartilage in Mandibular Development and DysmorphogenesisM Kathleen Pitirri, Emily L Durham, Natalie A Romano, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
A novel mouse model of rare neurodevelopmental disorder, TBCK SyndromeAshley J Melendez-Perez, Emily L Durham, Dana E Layo-Carris, et al.
HGG Advances|April 17, 2025
Coupling deep phenotypic quantification with next-generation phenotyping for 192 individuals with germline histonopathiesEmily E Lubin, Elizabeth M Gonzalez, Annabel K Sangree, et al.
European Journal of Human Genetics : EJHG|July 26, 2024
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individualsDana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
European Journal of Human Genetics : EJHG|April 27, 2024
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individualsDana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Biorxiv : the Preprint Server for Biology|October 3, 2025
TBCK Deficiency Alters Ribosomal Function, RNA Splicing, and miRNA Networks: Insights from Multi-Omics AnalysesAbdias Diaz-Rosado, Kelly Clark, Rajesh Angireddy, et al.
Frontiers in Genetics|June 2, 2022
Meckel's Cartilage in Mandibular Development and DysmorphogenesisM Kathleen Pitirri, Emily L Durham, Natalie A Romano, et al.
Biorxiv : the Preprint Server for Biology|May 25, 2026
A novel mouse model of rare neurodevelopmental disorder, TBCK SyndromeAshley J Melendez-Perez, Emily L Durham, Dana E Layo-Carris, et al.
HGG Advances|April 17, 2025
Coupling deep phenotypic quantification with next-generation phenotyping for 192 individuals with germline histonopathiesEmily E Lubin, Elizabeth M Gonzalez, Annabel K Sangree, et al.
European Journal of Human Genetics : EJHG|July 26, 2024
Correction: Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individualsDana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
European Journal of Human Genetics : EJHG|April 27, 2024
Expanded phenotypic spectrum of neurodevelopmental and neurodegenerative disorder Bryant-Li-Bhoj syndrome with 38 additional individualsDana E Layo-Carris, Emily E Lubin, Annabel K Sangree, et al.
Pageof 4