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Human Mutation
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May 31, 2019
Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI-5 intellectual disability challenge
Marco Carraro, Alexander Miguel Monzon, Luigi Chiricosta, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
September 8, 2016
Clinical Effects of Driver Somatic Mutations on the Outcomes of Patients With Myelodysplastic Syndromes Treated With Allogeneic Hematopoietic Stem-Cell Transplantation
Matteo G Della Porta, Anna Gallì, Andrea Bacigalupo, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project
Sarah L Stenton, Melanie O'Leary, Gabrielle Lemire, et al.
Human Genomics
|
April 29, 2024
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project
Sarah L Stenton, Melanie C O'Leary, Gabrielle Lemire, et al.
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Search research articles
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Showing results (21-30 of 24) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 24 results.
Human Mutation
|
May 31, 2019
Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI-5 intellectual disability challenge
Marco Carraro, Alexander Miguel Monzon, Luigi Chiricosta, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
September 8, 2016
Clinical Effects of Driver Somatic Mutations on the Outcomes of Patients With Myelodysplastic Syndromes Treated With Allogeneic Hematopoietic Stem-Cell Transplantation
Matteo G Della Porta, Anna Gallì, Andrea Bacigalupo, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 14, 2023
Critical assessment of variant prioritization methods for rare disease diagnosis within the Rare Genomes Project
Sarah L Stenton, Melanie O'Leary, Gabrielle Lemire, et al.
Human Genomics
|
April 29, 2024
Critical assessment of variant prioritization methods for rare disease diagnosis within the rare genomes project
Sarah L Stenton, Melanie C O'Leary, Gabrielle Lemire, et al.
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of 3