Whole-Genome Array CGH Evaluation for Replacing Prenatal Karyotyping in Hong Kong | PLOS ONE
Frontiers | Genetic Alterations in Essential Thrombocythemia Progression to Acute Myeloid Leukemia: A Case Series and Review of the Literature
Children | Free Full-Text | Identification of Extremely Rare Pathogenic CNVs by Array CGH in Saudi Children with Developmental Delay, Congenital Malformations, and Intellectual Disability
Genetic–pathologic characterization of myeloproliferative neoplasms | Experimental & Molecular Medicine
Occurrence of a paroxysmal nocturnal hemoglobinuria clone in an essential thrombocythemia: a link between <i>PIGV</i> and <i>MPL</i> | Haematologica
Frontiers | Genetic Alterations in Essential Thrombocythemia Progression to Acute Myeloid Leukemia: A Case Series and Review of the Literature
Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders | European Journal of Human Genetics
Derivative (1;18)(q10;q10) in essential thrombocythemia. | Semantic Scholar
Microarrays | Free Full-Text | SNP Array in Hematopoietic Neoplasms: A Review
Implementation of RNA sequencing and array CGH in the diagnostic workflow of the AIEOP-BFM ALL 2017 trial on acute lymphoblastic leukemia | springermedizin.de
Frontiers | Genetic Alterations in Essential Thrombocythemia Progression to Acute Myeloid Leukemia: A Case Series and Review of the Literature
Are we altering the natural history of primary myelofibrosis? - ScienceDirect
Allogeneic Hematopoietic Cell Transplantation for Advanced Polycythemia Vera and Essential Thrombocythemia - Biology of Blood and Marrow Transplantation
High-resolution whole genome tiling path array CGH analysis of CD34+ cells from patients with low-risk myelodysplastic syndromes reveals cryptic copy number alterations and predicts overall and leukemia-free survival - ScienceDirect
Genomic characterization of patients with polycythemia vera developing resistance to hydroxyurea | Leukemia
PDF) Systematization of analytical studies of polycythemia vera, essential thrombocythemia and primary myelofibrosis, and a meta-analysis of the frequency of JAK2, CALR and MPL mutations: 2000–2018
Frontiers | Genetic Alterations in Essential Thrombocythemia Progression to Acute Myeloid Leukemia: A Case Series and Review of the Literature
Genomic characterization of spleens in patients with myelofibrosis | Haematologica
Oligoarray comparative genomic hybridization in polycythemia vera and essential thrombocythemia | Haematologica
Systematization of analytical studies of polycythemia vera, essential thrombocythemia and primary myelofibrosis, and a meta-analysis of the frequency of JAK2, CALR and MPL mutations: 2000–2018 | BMC Cancer | Full Text
Systematization of analytical studies of polycythemia vera, essential thrombocythemia and primary myelofibrosis, and a meta-analysis of the frequency of JAK2, CALR and MPL mutations: 2000–2018 | BMC Cancer | Full Text
Full article: Mutation patterns in essential thrombocythemia, polycythemia vera and secondary myelofibrosis
Journal of Korean Medical Science
Cureus | 19p13.3 Deletion With Polyotia: A Case Report and Literature Review | Media
Cancers | Free Full-Text | The Prevalence of TET2 Gene Mutations in Patients with BCR-ABL-Negative Myeloproliferative Neoplasms (MPN): A Systematic Review and Meta-Analysis
