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Mariam T Mathew

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Clinical Chemistry|May 7, 2024
Optical Genome Mapping in Prenatal Diagnosis: Democratizing Comprehensive Cytogenomic TestingMariam T Mathew, Yassmine M N Akkari
Diagnostic Pathology|August 27, 2025
Bilateral, multicystic fumarate hydratase-deficient renal cell carcinoma in patient with hereditary leiomyomatosis & renal cell carcinoma syndrome: A case report and review of the literatureAshlie E Rubrecht, Jennifer H Aldrink, Patrick Warren, et al.
The Journal of Applied Laboratory Medicine|January 3, 2024
Clinical Cytogenetics: Current Practices and BeyondMariam T Mathew, Melanie Babcock, Ying-Chen Claire Hou, et al.
Pediatric Neurology|March 12, 2023
Deep Brain Stimulation for the Management of AIFM1-Related Disabling Tremor: A Case SeriesJude Tunyi, Nicolas J Abreu, Richa Tripathi, et al.
Cold Spring Harbor Molecular Case Studies|October 30, 2021
Somatic variation as an incidental finding in the pediatric next-generation sequencing eraMarilena Melas, Mariam T Mathew, Mari Mori, et al.
Cancers|September 9, 2023
Expanding the Clinical Utility of Targeted RNA Sequencing Panels beyond Gene Fusions to Complex, Intragenic Structural RearrangementsKathleen M Schieffer, Amanda Moccia, Brianna A Bucknor, et al.
Frontiers in Oncology|December 17, 2024
Comprehensive genomic characterization of hematologic malignancies at a pediatric tertiary care centerAnn M Kebede, Elizabeth A R Garfinkle, Mariam T Mathew, et al.
Neuro-Oncology Advances|July 22, 2024
Germline susceptibility from broad genomic profiling of pediatric brain cancersElaine R Mardis, Samara L Potter, Kathleen M Schieffer, et al.
Archives of Pathology & Laboratory Medicine|January 8, 2024
Multisite Verification of a Targeted CFTR Polymerase Chain Reaction/Capillary Electrophoresis Assay That Evaluates Pathogenic Variants Across Diverse Ethnic and Ancestral GroupsBradley Hall, John N Milligan, Kevin Kelnar, et al.
The American Journal of Surgical Pathology|September 26, 2023
Papillary Hemangioma Harbors Somatic GNA11 and GNAQ MutationsCatherine K Gestrich, Mathew P Vivero, Dennis J Konczyk, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Clinical Chemistry|May 7, 2024
Optical Genome Mapping in Prenatal Diagnosis: Democratizing Comprehensive Cytogenomic TestingMariam T Mathew, Yassmine M N Akkari
Diagnostic Pathology|August 27, 2025
Bilateral, multicystic fumarate hydratase-deficient renal cell carcinoma in patient with hereditary leiomyomatosis & renal cell carcinoma syndrome: A case report and review of the literatureAshlie E Rubrecht, Jennifer H Aldrink, Patrick Warren, et al.
The Journal of Applied Laboratory Medicine|January 3, 2024
Clinical Cytogenetics: Current Practices and BeyondMariam T Mathew, Melanie Babcock, Ying-Chen Claire Hou, et al.
Pediatric Neurology|March 12, 2023
Deep Brain Stimulation for the Management of AIFM1-Related Disabling Tremor: A Case SeriesJude Tunyi, Nicolas J Abreu, Richa Tripathi, et al.
Cold Spring Harbor Molecular Case Studies|October 30, 2021
Somatic variation as an incidental finding in the pediatric next-generation sequencing eraMarilena Melas, Mariam T Mathew, Mari Mori, et al.
Cancers|September 9, 2023
Expanding the Clinical Utility of Targeted RNA Sequencing Panels beyond Gene Fusions to Complex, Intragenic Structural RearrangementsKathleen M Schieffer, Amanda Moccia, Brianna A Bucknor, et al.
Frontiers in Oncology|December 17, 2024
Comprehensive genomic characterization of hematologic malignancies at a pediatric tertiary care centerAnn M Kebede, Elizabeth A R Garfinkle, Mariam T Mathew, et al.
Neuro-Oncology Advances|July 22, 2024
Germline susceptibility from broad genomic profiling of pediatric brain cancersElaine R Mardis, Samara L Potter, Kathleen M Schieffer, et al.
Archives of Pathology & Laboratory Medicine|January 8, 2024
Multisite Verification of a Targeted CFTR Polymerase Chain Reaction/Capillary Electrophoresis Assay That Evaluates Pathogenic Variants Across Diverse Ethnic and Ancestral GroupsBradley Hall, John N Milligan, Kevin Kelnar, et al.
The American Journal of Surgical Pathology|September 26, 2023
Papillary Hemangioma Harbors Somatic GNA11 and GNAQ MutationsCatherine K Gestrich, Mathew P Vivero, Dennis J Konczyk, et al.
Pageof 2