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Sean S Young

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

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European Journal of Human Genetics : EJHG|December 4, 2003
Alternatively spliced, truncated human BRCA2 isoforms contain a novel coding exonMarsha D Speevak, Sean S Young, Harriet Feilotter, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
Role of integrin-linked kinase in nerve growth factor-stimulated neurite outgrowthJulia Mills, Murat Digicaylioglu, Arthur T Legg, et al.
The Journal of Molecular Diagnostics : JMD|October 8, 2013
A clinically validated diagnostic second-generation sequencing assay for detection of hereditary BRCA1 and BRCA2 mutationsIan E Bosdet, T Roderick Docking, Yaron S Butterfield, et al.
The Journal of Molecular Diagnostics : JMD|July 1, 2021
Use of Treatment-Focused Tumor Sequencing to Screen for Germline Cancer PredispositionTammy T Y Lau, Christina M May, Zahra J Sefid Dashti, et al.
British Journal of Haematology|May 30, 2012
Allogeneic haematopoietic stem cell transplantation for chronic lymphocytic leukaemia: outcome in a 20-year cohortCynthia L Toze, Chinmay B Dalal, Thomas J Nevill, et al.
Journal of Medical Genetics|July 26, 2018
Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmapJeanna M McCuaig, Tracy L Stockley, Patricia Shaw, et al.
Cold Spring Harbor Molecular Case Studies|August 3, 2018
Corrigendum: Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline <i>CHEK2</i>:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinomaMy Linh Thibodeau, Caralyn Reisle, Eric Zhao, et al.
Cold Spring Harbor Molecular Case Studies|May 18, 2017
Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline <i>CHEK2</i>:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinomaMy Linh Thibodeau, Caralyn Reisle, Eric Zhao, et al.
Nature Communications|May 16, 2024
Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancersRebecca J Deyell, Yaoqing Shen, Emma Titmuss, et al.
Journal of Medical Genetics|April 20, 2021
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics RepositoryChloe Mighton, Amanda C Smith, Justin Mayers, et al.
Pageof 1

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

Sort By:
Pageof 1
European Journal of Human Genetics : EJHG|December 4, 2003
Alternatively spliced, truncated human BRCA2 isoforms contain a novel coding exonMarsha D Speevak, Sean S Young, Harriet Feilotter, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 12, 2003
Role of integrin-linked kinase in nerve growth factor-stimulated neurite outgrowthJulia Mills, Murat Digicaylioglu, Arthur T Legg, et al.
The Journal of Molecular Diagnostics : JMD|October 8, 2013
A clinically validated diagnostic second-generation sequencing assay for detection of hereditary BRCA1 and BRCA2 mutationsIan E Bosdet, T Roderick Docking, Yaron S Butterfield, et al.
The Journal of Molecular Diagnostics : JMD|July 1, 2021
Use of Treatment-Focused Tumor Sequencing to Screen for Germline Cancer PredispositionTammy T Y Lau, Christina M May, Zahra J Sefid Dashti, et al.
British Journal of Haematology|May 30, 2012
Allogeneic haematopoietic stem cell transplantation for chronic lymphocytic leukaemia: outcome in a 20-year cohortCynthia L Toze, Chinmay B Dalal, Thomas J Nevill, et al.
Journal of Medical Genetics|July 26, 2018
Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmapJeanna M McCuaig, Tracy L Stockley, Patricia Shaw, et al.
Cold Spring Harbor Molecular Case Studies|August 3, 2018
Corrigendum: Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline <i>CHEK2</i>:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinomaMy Linh Thibodeau, Caralyn Reisle, Eric Zhao, et al.
Cold Spring Harbor Molecular Case Studies|May 18, 2017
Genomic profiling of pelvic genital type leiomyosarcoma in a woman with a germline <i>CHEK2</i>:c.1100delC mutation and a concomitant diagnosis of metastatic invasive ductal breast carcinomaMy Linh Thibodeau, Caralyn Reisle, Eric Zhao, et al.
Nature Communications|May 16, 2024
Whole genome and transcriptome integrated analyses guide clinical care of pediatric poor prognosis cancersRebecca J Deyell, Yaoqing Shen, Emma Titmuss, et al.
Journal of Medical Genetics|April 20, 2021
Data sharing to improve concordance in variant interpretation across laboratories: results from the Canadian Open Genetics RepositoryChloe Mighton, Amanda C Smith, Justin Mayers, et al.
Pageof 1