Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Lucy C Fox

Showing results (21-30 of 38) with videos related to

Pageof 4
Sort By:
British Journal of Haematology|October 10, 2025
Genomic variation in DDX41 identified through clinical sequencingCelestine Wells, Ing Soo Tiong, Sally Hunter, et al.
Ejhaem|January 27, 2025
A novel TERT variant associated with a telomere biology disorder and challenges in variant classificationVahid Pazhakh, Lucy C Fox, Nicole Den Elzen, et al.
Leukemia|February 17, 2026
Refinement of the classification of DDX41 variants through analysis of aggregated clinical datasetsIng Soo Tiong, Sally Hunter, Yamuna Kankanige, et al.
Internal Medicine Journal|July 2, 2025
Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromesLucy C Fox, Erin Goode, Nicole Den Elzen, et al.
British Journal of Haematology|March 3, 2025
Heterozygous germline TET2 loss-of-function variants associated with an ALPS-like phenotypeSean Harrop, Joshua Casan, Hannah Rose, et al.
Internal Medicine Journal|October 17, 2018
Revisiting acquired aplastic anaemia: current concepts in diagnosis and managementDanielle B Clucas, Lucy C Fox, Erica M Wood, et al.
Internal Medicine Journal|March 28, 2018
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New ZealandLucy C Fox, Solomon J Cohney, Joshua Y Kausman, et al.
Nephrology (Carlton, Vic.)|February 9, 2018
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New ZealandLucy C Fox, Solomon J Cohney, Joshua Y Kausman, et al.
Blood Advances|April 27, 2022
Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorderAram Niaz, Jia Truong, Annabel Manoleras, et al.
British Journal of Haematology|June 4, 2020
A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variabilityLucy C Fox, Michelle Tan, Anna L Brown, et al.
Pageof 4

Showing results (21-30 of 38) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|October 10, 2025
Genomic variation in DDX41 identified through clinical sequencingCelestine Wells, Ing Soo Tiong, Sally Hunter, et al.
Ejhaem|January 27, 2025
A novel TERT variant associated with a telomere biology disorder and challenges in variant classificationVahid Pazhakh, Lucy C Fox, Nicole Den Elzen, et al.
Leukemia|February 17, 2026
Refinement of the classification of DDX41 variants through analysis of aggregated clinical datasetsIng Soo Tiong, Sally Hunter, Yamuna Kankanige, et al.
Internal Medicine Journal|July 2, 2025
Design, implementation and evaluation of a model of care for patients with germline predisposition to haematological malignancy and bone marrow failure syndromesLucy C Fox, Erin Goode, Nicole Den Elzen, et al.
British Journal of Haematology|March 3, 2025
Heterozygous germline TET2 loss-of-function variants associated with an ALPS-like phenotypeSean Harrop, Joshua Casan, Hannah Rose, et al.
Internal Medicine Journal|October 17, 2018
Revisiting acquired aplastic anaemia: current concepts in diagnosis and managementDanielle B Clucas, Lucy C Fox, Erica M Wood, et al.
Internal Medicine Journal|March 28, 2018
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New ZealandLucy C Fox, Solomon J Cohney, Joshua Y Kausman, et al.
Nephrology (Carlton, Vic.)|February 9, 2018
Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New ZealandLucy C Fox, Solomon J Cohney, Joshua Y Kausman, et al.
Blood Advances|April 27, 2022
Functional interaction between compound heterozygous TERT mutations causes severe telomere biology disorderAram Niaz, Jia Truong, Annabel Manoleras, et al.
British Journal of Haematology|June 4, 2020
A synonymous GATA2 variant underlying familial myeloid malignancy with striking intrafamilial phenotypic variabilityLucy C Fox, Michelle Tan, Anna L Brown, et al.
Pageof 4