Last Updated: 09/26/2026
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Found 22 publications
Cryptic to conventional cytogenetics: Philadelphia-like ALL presenting with hypereosinophilia.
Journal: BMJ case reports
Published: January 22, 2025
Prognostic Significance and Treatment Response Associations of Genetic Mutations in Chronic Myelomonocytic Leukemia: A Retrospective Cohort Study.
Journal: Biomedicines
Published: October 06, 2024
The Validation of Digital PCR-Based Minimal Residual Disease Detection for the Common Mutations in IDH1 and IDH2 Genes in Patients with Acute Myeloid Leukemia.
Journal: The Journal of molecular diagnostics : JMD
Published: May 14, 2024
Feasibility and Clinical Utility of Reporting Hereditary Cancer Predisposition Pathogenic Variants Identified in Research Germline Sequencing: A Prospective Interventional Study.
Journal: JCO precision oncology
Published: January 31, 2024
Optimising clinical care through CDH1-specific germline variant curation: improvement of clinical assertions and updated curation guidelines.
Journal: Journal of medical genetics
Published: July 06, 2022
Real-World Evaluation of a Population Germline Genetic Screening Initiative for Family Medicine Patients.
Journal: Journal of personalized medicine
Published: June 05, 2022
Diagnosis of Classic Homocystinuria in Two Boys Presenting with Acute Cerebral Venous Thrombosis and Neurologic Dysfunction after Normal Newborn Screening.
Journal: International journal of neonatal screening
Published: April 29, 2021
A Novel Approach to Improve Newborn Screening for Congenital Hypothyroidism by Integrating Covariate-Adjusted Results of Different Tests into CLIR Customized Interpretive Tools.
Journal: International journal of neonatal screening
Published: February 10, 2021
Acute undifferentiated leukemia: data on incidence and outcomes from a large population-based database.
Journal: Leukemia research
Published: November 17, 2019
Last Updated: 09/26/2026