• <em>RAD21</em> is a driver of chromosome 8 gain in Ewing sarcoma to mitigate replication stress
• A 46,XY Female with a 9p24.3p24.1 Deletion and a 8q24.11q24.3 Duplication: A Case Report and Review of the Literature
• A case of acute promyelocytic leukemia variant with derivative chromosome 3 der(3)t(3;8) associated with 8q partial gain
• A case of Behçet's-like disease associated with trisomy 8-positive myelodysplastic syndrome carrying MEFV E148Q variant presented with periodic fever
• A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin
• A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report
• A Rare Case of Hemophagocytic Lymphohistiocytosis Associated With Myelodysplastic Syndrome and Trisomy 8 in a Pediatric Patient
• A rare case of hepatosplenic γδ T-cell lymphoma expressing CD19 with ring chromosome 7 and trisomy 8
• A rare case of partial trisomy 8q24.12-q24.3 and partial monosomy of 8q24.3: Prenatal diagnosis and clinical findings
• A simple method to allow for guanine-cytosine amplification error in prenatal DNA screening for trisomy 18
• Acute Myelogenous Leukemia With Trisomy 8 and Concomitant Acquired Factor VII Deficiency
• Airway compression after pulmonary artery banding
• Allogeneic stem cell transplantation for trisomy 8-positive myelodysplastic syndrome or myelodysplastic/myeloproliferative disease with refractory Behçet's disease: Case report and the review of literature
• An unusual case of trisomy 8 mosaicism complicated by coexistence of phenylketonuria
• Análisis de la presencia de trisomía 8 en las diferentes fases de leucemia mieloide crónica
• Autoimmune and inflammatory manifestations associated with acute myeloid leukemia with Trisomy 8-Case series and review of the literature
• BCR/ABL1 fluorescence <em>in situ</em> hybridization fusion signals on both copies of chromosome 22 in a Philadelphia-masked chronic myeloid leukemia case: implication for the therapy
• Behçet disease (BD) and BD-like clinical phenotypes: NF-κB pathway in mucosal ulcerating diseases
• Behçet's-like syndrome and other dysimmunitary manifestations related to myelodysplastic syndromes with trisomy 8
• Better leukemia-free survival with allogeneic than with autologous HCT in AML patients with isolated trisomy 8: a study from the ALWP of the EBMT
• Bilateral severe microphthalmia in a neonate with trisomy 8 mosaicism: A new finding
• Cell-free DNA analysis in maternal blood: comparing genome-wide versus targeted approach as a first-line screening test
• Chimerism 47,XY, + 8/46,XX: Follow-up for 11 Years
• Chromosomal abnormalities related to fever of unknown origin in a Chinese pediatric cohort and literature review
• Chromosomal imbalance in pigs showing a syndromic form of cleft palate
• Clinical and genetic analysis of a child with mosaic chromosome 8 trisomy syndrome
• Clinical and molecular characterization of patients with acute myeloid leukemia and sole trisomies of chromosomes 4, 8, 11, 13 or 21
• Clinical features and independent predictors of Behçet's disease associated with myelodysplastic syndrome
• Clinical features and prognosis of patients with gastrointestinal Behçet's disease-like syndrome and myelodysplastic syndrome with and without trisomy 8
• Clinical impact of MYC abnormalities in plasma cell myeloma
• Clinical Significance of Additional Chromosomal 8 Clonal Evolution in CML Progression
• Clinical significance of cytogenetic and molecular genetic abnormalities in 634 Chinese patients with myelodysplastic syndromes
• Clonal evolution and clinical significance of trisomy 8 in acquired bone marrow failure
• Co-occurrence of PML-RARA gene fusion, chromosome 8 trisomy, and FLT3 ITD mutation in a young female patient with de novo acute myeloid leukemia and early death: A CARE case report
• Congenital Corneal Opacities Associated With Trisomy 8 Mosaicism Syndrome
• Cytogenetic profile of patients with clinical spectrum of ambiguous genitalia, amenorrhea, and Turner phenotype: A 21-year single-center experience
• Developing immortal cell lines from <em>Xenopus</em> embryos<em>,</em> four novel cell lines derived from <em>Xenopus tropicalis</em>
• Disappearance of the trisomy 8 cell line at long-term follow-up in mosaic trisomy 8 at amniocentesis in a pregnancy with a favorable outcome
• Divergent leukaemia subclones as cellular models for testing vulnerabilities associated with gains in chromosomes 7, 8 or 18
• Drug resistance in diploid yeast is acquired through dominant alleles, haploinsufficiency, gene duplication and aneuploidy
• Dysregulated KRAS gene-signaling axis and abnormal chromatin remodeling drive therapeutic resistance in heterogeneous-sized circulating tumor cells in gastric cancer patients
• Early and Innovative Rehabilitation in Warkany Syndrome 2 Associated with Agenesis of the Corpus Callosum: A Case Report
• Effectiveness of Chromosomal Microarray Analysis for Prenatal Diagnosis of Fetal Echogenic Intracardiac Focus: A Single-Center Experience
• Establishment and validation of prognostic nomogram in acute leukemia with trisomy 8
• Expression of ERV3-1 in leukocytes of acute myelogenous leukemia patients
• First trimester prenatal detection of mosaic trisomy 8
• Gastrointestinal Behcet's-like disease with myelodysplastic neoplasms with trisomy 8: a French case series and literature review
• Generation of a novel isogenic trisomy panel in human embryonic stem cells via microcell-mediated chromosome transfer
• Genetic analysis of a case with a supernumerary marker derived from chromosome 9
• Genetic and Transcriptional Analysis of 8q24.21 Cluster in Gastric Cancer
• Hemophagocytic lymphohistiocytosis and myelodysplastic syndrome: a case report and review of the literature
• Hemophagocytic lymphohystiocytosis after haemolytic transfusion reaction due to anti-Wr^a in a patient with myelodysplastic syndrome
• Hidradenitis suppurativa in a patient with Warkany syndrome: Sustainability of adalimumab treatment
• High Incidence of Gastrointestinal Ulceration and Cytogenetic Aberration of Trisomy 8 as Typical Features of Behçet's Disease Associated with Myelodysplastic Syndrome: A Series of 16 Consecutive Chinese Patients from the Shanghai Behçet's Diseas
• Inflammatory disorders associated with trisomy 8-myelodysplastic syndromes: French retrospective case-control study
• Intestinal Behçet disease associated with myelodysplastic syndrome accompanying trisomy 8 successfully treated with abdominal surgery followed by hematopoietic stem cell transplantation: A case report
• Intestinal Behçet's Disease with Primary Myelofibrosis Involving Trisomy 8
• Karyotyping and prenatal diagnosis of 47,XX,+ 8[67]/46,XX [13] Mosaicism: case report and literature review
• Laboratory divergences in concurrent diagnosis of acute myeloid leukemia relapse and COVID-19: A case report
• Leukocyte Nucleus Reveals a Linear Order of Chromosomes Separated in Two Parental Genomes That Favors the Process of Gene Activation
• Long-term maintenance of the mucosal healing induced by azacitidine therapy in a patient with intestinal Behçet's-like disease accompanied with myelodysplastic syndrome involving trisomy 8
• Longitudinal detection of subcategorized CD44v6⁺ CTCs and circulating tumor endothelial cells (CTECs) enables novel clinical stratification and improves prognostic prediction of small cell lung cancer: A prospective, multi-center st
• Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 associated with congenital hypoplasia of the tongue and review of the literature
• Molecular genetic and clinical characterization of acute myeloid leukemia with trisomy 8 as the sole chromosome abnormality
• Molecular investigation of uniparental disomy (UPD) in spontaneous abortions
• Mosaic Small Supernumerary Marker Chromosome Derived from Five Discontinuous Regions of Chromosome 8 in a Patient with Neutropenia and Oral Aphthous Ulcer
• Myelodysplastic syndrome (MDS) with isolated trisomy 8: a type of MDS frequently associated with myeloproliferative features? A report by the Groupe Francophone des Myélodysplasies
• Myelodysplastic syndrome with trisomy 8 related multiple intestinal ulcers: a case report
• Neurodevelopmental phenotype in 36 new patients with 8p inverted duplication-deletion: Genotype-phenotype correlation for anomalies of the corpus callosum
• Non-balanced translocation between the short arms of chromosomes 8 and 6 associated with type 1 diabetes mellitus
• Occurrence of acute myeloid leukemia in hydroxyurea-treated sickle cell disease patient
• Optimal Treatment Approaches to Intestinal Behçet's Disease Complicated by Myelodysplastic Syndrome: The KASID and KSBD Multicenter Study
• Partial Trisomy of Chromosome 13 with a Novel Translocation (8 ; 13) and Unique Clinical Presentation in a Palestinian Infant
• Prenatal and postnatal diagnoses and phenotype of 8p23.3p22 duplication in one family
• Prenatal diagnosis and genetic counseling of a uniparental isodisomy of chromosome 8 with no phenotypic abnormalities
• Prenatal diagnosis of 18p deletion and 8p trisomy syndrome: literature review and report of a novel case
• Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
• Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal
• Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening
• Primary myelofibrosis but not autoimmune myelofibrosis accompanied by Sjögren's syndrome and primary biliary cirrhosis in a patient with trisomy 8 mosaic: a case report and literature review
• Prognosis influence of additional chromosome abnormalities in newly diagnosed acute promyelocytic leukemia with t(15;17)(q24;q21)
• Rare additional chromosomal abnormalities in acute promyelocytic leukaemia resulting in rapidly fatal disease: report of a case
• Recurrent Acute Myocardial Infarction With Systemic Thromboembolism May Indicate an Underlying Etiology
• Recurring germline mosaicism in a family due to reversion of an inherited derivative chromosome 8 from an 8;21 translocation with interstitial telomeric sequences
• Retinal abnormalities in three genetic disorders involving the X chromosome
• Severe Inflammatory Response in Myelodysplastic Syndrome and Trisomy 8 Following 23-Valent Polysaccharide Pneumococcal Vaccine Administration
• Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance
• Splenic marginal zone lymphoma with a de novo t(8;14)(q24;q32) and a prolymphocytoid evolution responsive to rituximab-bendamustine
• Spontaneous remission of acute monocytic leukemia with trisomy 8 and trisomy 18
• Successful treatment by thalidomide therapy of intestinal Behçet's disease associated with trisomy 8 myelodysplastic syndrome
• The incidental discovery of a constitutional trisomy 21 mosaicism in an adult female with myelodysplastic/myeloproliferative neoplasm
• The RS4;11 cell line as a model for leukaemia with t(4;11)(q21;q23): Revised characterisation of cytogenetic features
• Trisomy 8 Defines a Distinct Subtype of Myeloproliferative Neoplasms Driven by the MYC-Alarmin Axis
• Trisomy 8 in acute myeloid leukemia
• Trisomy 8 mosaicism in the placenta: A Danish cohort study of 37 cases and a literature review
• Trisomy 8-positive Polycythemia Vera Complicated with Intestinal Behçet's-like Disease: A New Perspective for a Clinical Approach
• Trisomy-8-Positive Hematologic Malignancies Associated with Intestinal Behçet's Syndrome: Keep This Entity in Mind
• 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
• UBTF-internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia
• Upregulation of microRNA-597 in myelodysplastic syndromes induces apoptosis through FOSL2 inhibition