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3. Clinical utility of next‐generation sequencing in the diagnosis of hereditary haemolytic anaemias. (12th June 2016)

4. Clinical utility of targeted next‐generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experience. (8th March 2023)

5. Clinicopathologic characteristics of myeloproliferative neoplasms with JAK2 exon 12 mutation. (April 2023)

7. Concurrent detection of targeted copy number variants and mutations using a myeloid malignancy next generation sequencing panel allows comprehensive genetic analysis using a single testing strategy. (5th January 2016)

8. De Novo Acute Myeloid Leukemia in Adults: Suppression of MicroRNA-223 is Independent of LMO2 Protein Expression BUT Associate With Adverse Cytogenetic Profile and Undifferentiated Blast Morphology. Issue 10 (November 2015)

10. Real‐world diagnostic testing patterns for assessment of ring sideroblasts and SF3B1 mutations in patients with newly diagnosed lower‐risk myelodysplastic syndromes. (21st November 2020)