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Acute Promyelocytic Leukemia Lacking the Classic Translocation t(15;17)

Introduction Acute promyelocytic leukemia (APL) is a subtype of acute myeloid leukemia (AML) characterized by the reciprocal translocation t(15;17)(q22;q12) resulting…

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Cytogenetic and Molecular Characterization of a Partial Trisomy 2p Arising From Inverted Duplication of 2p With Terminal Deletion of 2pter

Abstract Partial trisomy 2p is typically associated with partial monosomy of another chromosomal segment and results from a balanced translocation…

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Recombinant Chromosome 7 in a Mosaic 45,X/47,XXX Patient

Introduction Individuals with pericentric inversions are at risk for producing offspring with chromosomal gains and losses, while those carrying paracentric…

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Acute myeloid leukemia with t(7;21)(p22;q22) and 5q deletion: a case report and literature review

Abstract The gene RUNX1 at chromosome 21q22 encodes the alpha subunit of Core binding factor (CBF), a heterodimeric transcription factor…

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Genomic profiling using array comparative genomic hybridization define distinct subtypes of diffuse large b-cell lymphoma: a review of the literature

Abstract Diffuse large B-cell lymphoma (DLBCL) is the most common type of non-Hodgkin Lymphoma comprising of greater than 30% of…

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JAK2 Translocations in Hematological Malignancies: Review of the Literature

Abstract JAK2 is a cytoplasmic tyrosine kinase whose gene is located on chromosome 9p24. It is involved in the regulation…

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Acute myeloid leukemia with inv(16) with CBFBe-MYH11, 30CBFB deletion, variant t(9;22) with BCReABL1, and del(7)(q22q32) in apediatric patient: case report and literature review

Abstract Coexistence of inv(16)andt(9;22)is a rare chromosomal aberration, one that has been described in chronic myelogenous leukemia (CML), mainly in…

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Epigenetics

Genomic Imprinting Genomic imprinting is caused by alterations in chromatin in certain locations of the genome that occur in the…

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