• <em>LAG3</em> and Its Ligands Show Increased Expression in High-Risk Uveal Melanoma
• 3p interstitial deletion including PRICKLE2 in identical twins with autistic features
• A case of 3p deletion syndrome associated with cerebellar hemangioblastoma
• Aberrant MicroRNA Expression and Its Implications for Uveal Melanoma Metastasis
• Adapted whole-body surveillance for von Hippel-Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report
• Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes
• Aqueous Humor Biomarkers Identify Three Prognostic Groups in Uveal Melanoma
• BAP1 Immunostain Status in Intraocular Biopsy Specimens for Uveal Melanoma Highly Correlates with Other Prognostic Markers
• Chromosome r(3)(p25.3q29) in a Patient with Developmental Delay and Congenital Heart Defects: A Case Report and a Brief Literature Review
• Clinicopathologic study of primary renal hemangioblastoma
• Complex translocation among chromosomes 2, 3, 9, 15, 18, 20 in a patient with 3p-syndrome
• Cytogenetic Abnormalities for Predicting the Risk of Metastases in Choroidal and Ciliary Body Melanoma
• Development of synchronous VHL syndrome tumors reveals contingencies and constraints to tumor evolution
• Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent <em>in Situ</em> Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangeme
• Genetic landscape of uveal melanoma
• In uveal melanoma Gα-protein GNA11 mutations convey a shorter disease-specific survival and are more strongly associated with loss of BAP1 and chromosomal alterations than Gα-protein GNAQ mutations
• Lacrimal drainage anomalies in 3p deletion syndrome
• Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy
• Multi-tiered genomic analysis of head and neck cancer ties TP53 mutation to 3p loss
• Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype
• Phenotypic and genetic analysis of a boy with 3p26.3-pter deletion and 7q31.33-qter duplication
• Prognostic Factors Five Years After Enucleation for Uveal Melanoma
• Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma
• Schizophrenia and epilepsy as a result of maternally inherited CNTN6 copy number variant
• The prognostic value of extraocular extension in relation to monosomy 3 and gain of chromosome 8q in uveal melanoma
• Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes
• Uveal melanoma - testing of abnormalities of chromosome 3 and 8 in the Czech Republic