• 8q13.1-q13.2 deletion associated with inferior cerebellar vermian hypoplasia and digital anomalies: a new syndrome?
• A Case Report of Respiratory Syncytial Virus-Infected 8p Inverted Duplication Deletion Syndrome with Low Natural Killer Cell Activity
• A cluster of cooperating tumor-suppressor gene candidates in chromosomal deletions
• A Peculiar CLL Case with Complex Chromosome 6 Rearrangements and Refinement of All Breakpoints at the Gene Level by Genomic Array: A Case Report
• Bicuspid Aortic Valve-Associated Regulatory Regions Reveal <em>GATA4</em> Regulation and Function During Human-Induced Pluripotent Stem Cell-Based Endothelial-Mesenchymal Transition-Brief Report
• Characterization of Potential Molecular Markers in Lac Insect <em>Kerria lacca</em> (Kerr) Responsible for Lac Production
• Chromosomal abnormalities related to fever of unknown origin in a Chinese pediatric cohort and literature review
• Clinical characterization and genetic analysis of a newborn with chromosome 8q21.11 deletion syndrome
• Clinical characterization of a male patient with the recently described 8q21.11 microdeletion syndrome
• Confirmation of the human cathepsin B gene (CTSB) assignment to chromosome 8
• De novo centromere formation in pericentromeric region of rice chromosome 8
• Deletion of chromosome 8q22.1, a critical region for Nablus mask-like facial syndrome: four additional cases support a role of genetic modifiers in the manifestation of the phenotype
• Delineation of clinical course, outcomes, and prognostic factors in patients with T-cell prolymphocytic leukemia
• Fine Mapping and Identification of <em>SmAPRR2</em> Regulating Rind Color in Eggplant (<em>Solanum melongena</em> L.)
• Genetic analysis of a case with a supernumerary marker derived from chromosome 9
• Genome wide analysis in a family with sensorineural hearing loss, autism and mental retardation
• Identification and characterization of a novel gene controlling floral organ number in rice (Oryza sativa L.)
• Identification of salt stress-tolerant candidate genes in the BC₂F₂ population at the seedling stages of <em>G. hirsutum</em> and <em>G. darwinii</em> using NGS-based bulked segregant a
• Loss of 6q or 8p23 is associated with the total number of DNA copy number aberrations in adenoid cystic carcinoma
• Mutations in the <em>SmAPRR2</em> transcription factor suppressing chlorophyll pigmentation in the eggplant fruit peel are key drivers of a diversified colour palette
• Nicotinic Receptor Mutation in a Mildly Dysmorphic Girl with Duane Retraction Syndrome
• Novel 12 Mb interstitial deletion of chromosome 8p11.22-p21.2: a case report
• Prenatal diagnosis and molecular cytogenetic characterization of a de novo interchromosomal insertion of ins(1;8)(p22.1;q22q23)
• Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound
• Prenatal diagnosis of two fetuses with deletions of 8p23.1, critical region for congenital diaphragmatic hernia and heart defects
• Rare additional chromosomal abnormalities in acute promyelocytic leukaemia resulting in rapidly fatal disease: report of a case
• Ring chromosome 8 and translocation t(8;21) in a patient with acute myeloblastic leukemia
• SH2D4A downregulation due to loss of chromosome 8p is associated with poor prognosis and low T cell infiltration in colorectal cancer
• TRAPPC9-related neurodevelopmental disorder: Report of a homozygous deletion in TRAPPC9 due to paternal uniparental isodisomy
• Trichorhinophalangeal syndrome type II without the chromosome 8 deletion that resembled metachondromatosis