20 results on '"Peterson, Jess F"'
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2. Typical, atypical and cryptic t(15;17)(q24;q21) ( PML::RARA ) observed in acute promyelocytic leukemia: A retrospective review of 831 patients with concurrent chromosome and PML::RARA dual‐color dual‐fusion FISH studies
3. Spurious CD34 expression in B‐cell lymphoma due to nonspecific binding to PerCP‐Cy5 .5 fluorochrome conjugates: A rare phenomenon and a diagnostic pitfall
4. Comparative study of therapy‐related and de novo adult b‐cell acute lymphoblastic leukaemia
5. Increased complexity of t(11;14) rearrangements in plasma cell neoplasms compared with mantle cell lymphoma
6. Identification of a novelKMT2A / GIMAP8gene fusion in a pediatric patient with acute undifferentiated leukemia
7. Cryptic and atypical KMT2A‐USP2 and KMT2A‐USP8 rearrangements identified by mate pair sequencing in infant and childhood leukemia
8. Clinical utility of fluorescence in situ hybridization‐based diagnosis of BCR‐ABL1 like ( P hiladelphia chromosome like) B ‐acute lymphoblastic leukemia
9. Fluorescence in‐situ hybridisation for TP63 rearrangements in T cell lymphomas: single‐site experience of 470 patients and implications for clinical testing
10. Acute leukemias harboring KMT2A/MLLT10 fusion: a 10‐year experience from a single genomics laboratory
11. A near‐haploid clone harboring aBCR/ABL1gene fusion in an adult patient with newly diagnosed B‐lymphoblastic leukemia
12. Cover Image
13. Mate pair sequencing improves detection of genomic abnormalities in acute myeloid leukemia
14. KMT2A (MLL) rearrangements observed in pediatric/young adult T-lymphoblastic leukemia/lymphoma: A 10-year review from a single cytogenetic laboratory
15. Leukemic phase and CSF involvement of diffuse large B-cell lymphoma with a complex karyotype including a TP53 deletion
16. Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndrome
17. Elucidating discrepant results in a prenatal diagnosis of 48,XXY,+18 (Edwards and Klinefelter syndromes)
18. Craniofacial abnormalities and developmental delay in two families with overlapping 22q12.1 microdeletions involving the MN1 gene
19. Absence of skeletal anomalies in siblings with a maternally inherited 12q13.13-q13.2 microdeletion partially involving theHOXCgene cluster
20. Familial microduplication of 17q23.1-q23.2 involving TBX4 is associated with congenital clubfoot and reduced penetrance in females
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