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Kirsten M Farncombe

Showing results (1-10 of 21) with videos related to

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BMC Medical Genomics|July 15, 2022
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosisKirsten M Farncombe, Emily Thain, Carolina Barnett-Tapia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2022
Clinical implementation of genetic testing in adults for hereditary hematologic malignancy syndromesSafa Ansar, Janet Malcolmson, Kirsten M Farncombe, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 27, 2023
Retrospective Analysis of Canadian Adults with Tuberous Sclerosis ComplexDominique Pal, Nicole Forster, Monika Madan, et al.
Ophthalmic Genetics|March 28, 2023
Oncologist-led germline genetic testing for uveal melanomaBrittany Gillies, Hatem Krema, Anning Chao, et al.
NPJ Genomic Medicine|October 21, 2020
Early-onset renal cell carcinoma in <i>PTEN</i> harmatoma tumour syndromeRaymond H Kim, Xiangling Wang, Andrew J Evans, et al.
NPJ Genomic Medicine|March 19, 2022
VHL mosaicism: the added value of multi-tissue analysisLeslie E Oldfield, Jessica Grzybowski, Sylvie Grenier, et al.
Database : the Journal of Biological Databases and Curation|January 8, 2023
Developing a disease-specific annotation protocol for VHL gene curation using Hypothes.isDena Salehipour, Kirsten M Farncombe, Veronica Andric, et al.
NPJ Genomic Medicine|July 20, 2021
Incidental findings from cancer next generation sequencing panelsNika Maani, Karen Panabaker, Jeanna M McCuaig, et al.
Familial Cancer|July 22, 2023
Germline whole genome sequencing in adults with multiple primary tumorsYiming Wang, Qiliang Ding, Stephenie Prokopec, et al.
BMC Cancer|January 30, 2025
Clinical integration of germline findings from a tumor testing precision medicine programMaria Carolina Sanabria-Salas, Nina C Anggala, Brittany Gillies, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
BMC Medical Genomics|July 15, 2022
LZTR1 molecular genetic overlap with clinical implications for Noonan syndrome and schwannomatosisKirsten M Farncombe, Emily Thain, Carolina Barnett-Tapia, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 16, 2022
Clinical implementation of genetic testing in adults for hereditary hematologic malignancy syndromesSafa Ansar, Janet Malcolmson, Kirsten M Farncombe, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|December 27, 2023
Retrospective Analysis of Canadian Adults with Tuberous Sclerosis ComplexDominique Pal, Nicole Forster, Monika Madan, et al.
Ophthalmic Genetics|March 28, 2023
Oncologist-led germline genetic testing for uveal melanomaBrittany Gillies, Hatem Krema, Anning Chao, et al.
NPJ Genomic Medicine|October 21, 2020
Early-onset renal cell carcinoma in <i>PTEN</i> harmatoma tumour syndromeRaymond H Kim, Xiangling Wang, Andrew J Evans, et al.
NPJ Genomic Medicine|March 19, 2022
VHL mosaicism: the added value of multi-tissue analysisLeslie E Oldfield, Jessica Grzybowski, Sylvie Grenier, et al.
Database : the Journal of Biological Databases and Curation|January 8, 2023
Developing a disease-specific annotation protocol for VHL gene curation using Hypothes.isDena Salehipour, Kirsten M Farncombe, Veronica Andric, et al.
NPJ Genomic Medicine|July 20, 2021
Incidental findings from cancer next generation sequencing panelsNika Maani, Karen Panabaker, Jeanna M McCuaig, et al.
Familial Cancer|July 22, 2023
Germline whole genome sequencing in adults with multiple primary tumorsYiming Wang, Qiliang Ding, Stephenie Prokopec, et al.
BMC Cancer|January 30, 2025
Clinical integration of germline findings from a tumor testing precision medicine programMaria Carolina Sanabria-Salas, Nina C Anggala, Brittany Gillies, et al.
Pageof 3