Partial karyotypes from 3 patients with jumping translocation of the... | Download Scientific Diagram
PDF) Cell-autonomous megakaryopoiesis associated with polyclonal hematopoiesis in triple-negative essential thrombocythemia
Morphologic and cytogenetic differences between post-polycythemic myelofibrosis and primary myelofibrosis in fibrotic stage | Modern Pathology
Post-Essential Thrombocythemia Myelofibrosis and Multiple Isodicentric Y Chromosomes: A Unique Case among a Rare Association | Request PDF
The Pseudoautosomal Regions and Genes. Schematic of the X and Y sex... | Download Scientific Diagram
Two Y chromosomes with duplication of the distal long arm including the entire AZFc region - ScienceDirect
Cancers | Free Full-Text | Clinical Features, Gene Alterations, and Outcomes in Prefibrotic and Overt Primary and Secondary Myelofibrotic Patients
How Are Changes in the Chromosome 17 Related to Health Conditions? - StoryMD
Frontiers | Mutations, inflammation and phenotype of myeloproliferative neoplasms
Somatic Mutations of Calreticulin in Myeloproliferative Neoplasms | NEJM
High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21 - ScienceDirect
Genes | Free Full-Text | Genetic Background of Polycythemia Vera
A distinct molecular mutational profile and its clinical impact in essential thrombocythemia and primary myelofibrosis patients | BMC Cancer | Full Text
Germline-somatic JAK2 interactions are associated with clonal expansion in myelofibrosis | Nature Communications
Cytogenetic abnormalities in essential thrombocythemia: Clinical and molecular correlates and prognostic relevance in 809 informative cases | Blood Cancer Journal
IJMS | Free Full-Text | Congenital Diseases of DNA Replication: Clinical Phenotypes and Molecular Mechanisms
Clinical and molecular characteristics of forty Chinese children with essential thrombocythemia: A single‐center, retrospective analysis - Zhang - British Journal of Haematology - Wiley Online Library
Revised cytogenetic risk stratification in primary myelofibrosis: analysis based on 1002 informative patients | Leukemia
Rare Chromosomal Anomaly disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials
Essential Thrombocythemia - Ask Hematologist | Understand Hematology
A distinct molecular mutational profile and its clinical impact in essential thrombocythemia and primary myelofibrosis patients | BMC Cancer | Full Text
PDF) Cytogenetic abnormalities in essential thrombocythemia at presentation and transformation
The JAK2 46/1 haplotype confers susceptibility to essential thrombocythemia regardless of JAK2V617F mutational status—clinical correlates in a study of 226 consecutive patients | Leukemia
47,XYY,dup(13q12.11),t(4;9)(q21.1 ;q22.3),r(21)(p12q22.3) with Azoospermia and Low Intelligence | Reproductive and Developmental Medicine
Genetic–pathologic characterization of myeloproliferative neoplasms | Experimental & Molecular Medicine
