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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 14, 2012
Molecular genetic testing for fragile X syndrome: laboratory performance on the College of American Pathologists proficiency surveys (2001-2009)
Karen E Weck, Barbara Zehnbauer, Michael Datto, et al.
Journal of Pathology Informatics
|
November 17, 2025
Retrieval-augmented generation for interpreting clinical laboratory regulations using large language models
Suparna Nanua, Raven Steward, Benjamin Neely, et al.
The Journal of Applied Laboratory Medicine
|
November 3, 2024
Addressing False Positives in High-Sensitivity Troponin I Testing: Mitigation Strategies
Ruhan Wei, Bruce Lobaugh, Donna Kirsch, et al.
Journal of Pediatric Hematology/Oncology
|
September 26, 2012
Report of a young girl with MYH9 mutation and review of the literature
Daniel Landi, Evelyn Lockhart, Sara E Miller, et al.
Leukemia & Lymphoma
|
March 25, 2010
Histiocytic sarcoma arising in indolent small B-cell lymphoma: report of two cases with molecular/genetic evidence suggestive of a 'transdifferentiation' during the clonal evolution
Endi Wang, Charles Blake Hutchinson, Qin Huang, et al.
Brain Pathology (Zurich, Switzerland)
|
July 26, 2008
Chordoid glioma: a case report and molecular characterization of five cases
Craig Horbinski, Sanja Dacic, Roger E McLendon, et al.
Leukemia & Lymphoma
|
November 3, 2011
Molecular detection of circulating Sezary cells in patients with mycosis fungoides: could it predict future development of secondary Sezary syndrome? A single-institution experience
Charles Blake Hutchinson, Maggie Stoecker, Frances F Wang, et al.
The American Journal of Surgical Pathology
|
February 15, 2011
Sequential development of histiocytic sarcoma and diffuse large b-cell lymphoma in a patient with a remote history of follicular lymphoma with genotypic evidence of a clonal relationship: a divergent (bilineal) neoplastic transformation of an indolent B-cell lymphoma in a single individual
Endi Wang, John Papalas, Charles Blake Hutchinson, et al.
Genome Medicine
|
December 5, 2014
Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding
Susanne B Haga, Rachel Mills, Kathryn I Pollak, et al.
JCO Precision Oncology
|
February 9, 2022
Characterization of the Epidermal Growth Factor Receptor T790M Mutation in Colorectal Cancer
Erdem Altunel, Abed Alhalim Aljamal, John Mantyh, et al.
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Search research articles
Search
Showing results (1-10 of 19) with videos related to
Sort By:
Page
of 2
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
January 14, 2012
Molecular genetic testing for fragile X syndrome: laboratory performance on the College of American Pathologists proficiency surveys (2001-2009)
Karen E Weck, Barbara Zehnbauer, Michael Datto, et al.
Journal of Pathology Informatics
|
November 17, 2025
Retrieval-augmented generation for interpreting clinical laboratory regulations using large language models
Suparna Nanua, Raven Steward, Benjamin Neely, et al.
The Journal of Applied Laboratory Medicine
|
November 3, 2024
Addressing False Positives in High-Sensitivity Troponin I Testing: Mitigation Strategies
Ruhan Wei, Bruce Lobaugh, Donna Kirsch, et al.
Journal of Pediatric Hematology/Oncology
|
September 26, 2012
Report of a young girl with MYH9 mutation and review of the literature
Daniel Landi, Evelyn Lockhart, Sara E Miller, et al.
Leukemia & Lymphoma
|
March 25, 2010
Histiocytic sarcoma arising in indolent small B-cell lymphoma: report of two cases with molecular/genetic evidence suggestive of a 'transdifferentiation' during the clonal evolution
Endi Wang, Charles Blake Hutchinson, Qin Huang, et al.
Brain Pathology (Zurich, Switzerland)
|
July 26, 2008
Chordoid glioma: a case report and molecular characterization of five cases
Craig Horbinski, Sanja Dacic, Roger E McLendon, et al.
Leukemia & Lymphoma
|
November 3, 2011
Molecular detection of circulating Sezary cells in patients with mycosis fungoides: could it predict future development of secondary Sezary syndrome? A single-institution experience
Charles Blake Hutchinson, Maggie Stoecker, Frances F Wang, et al.
The American Journal of Surgical Pathology
|
February 15, 2011
Sequential development of histiocytic sarcoma and diffuse large b-cell lymphoma in a patient with a remote history of follicular lymphoma with genotypic evidence of a clonal relationship: a divergent (bilineal) neoplastic transformation of an indolent B-cell lymphoma in a single individual
Endi Wang, John Papalas, Charles Blake Hutchinson, et al.
Genome Medicine
|
December 5, 2014
Developing patient-friendly genetic and genomic test reports: formats to promote patient engagement and understanding
Susanne B Haga, Rachel Mills, Kathryn I Pollak, et al.
JCO Precision Oncology
|
February 9, 2022
Characterization of the Epidermal Growth Factor Receptor T790M Mutation in Colorectal Cancer
Erdem Altunel, Abed Alhalim Aljamal, John Mantyh, et al.
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of 2