3p Deletion Syndrome Latest Advances

Missegregation of Chromosome 3 and Generation of Monosomy 3 in the Proliferating Uveal Melanoma Cells Under Hyperglycemia.

Journal: Investigative ophthalmology & visual science

Published: December 02, 2025

BAP1 Loss on Immunocytochemistry and Its Association With Monosomy 3 in Uveal Melanoma Fine-Needle Aspirations.

Journal: Diagnostic cytopathology

Published: April 11, 2025

Lacrimal drainage anomalies in 3p deletion syndrome.

Journal: Orbit (Amsterdam, Netherlands)

Published: November 14, 2022

Adapted whole-body surveillance for von Hippel-Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report.

Journal: Pediatric blood & cancer

Published: March 11, 2022

Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements.

Journal: Balkan journal of medical genetics : BJMG

Published: April 05, 2021

Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy.

Journal: International journal of molecular sciences

Published: October 31, 2020

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.

Journal: BMC medical genetics

Published: June 20, 2019

Schizophrenia and epilepsy as a result of maternally inherited CNTN6 copy number variant.

Journal: Schizophrenia research

Published: June 02, 2018

Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma.

Journal: Genes, chromosomes & cancer

Published: January 12, 2018

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).

Journal: Taiwanese journal of obstetrics & gynecology

Published: February 24, 2016

Chromosome r(3)(p25.3q29) in a Patient with Developmental Delay and Congenital Heart Defects: A Case Report and a Brief Literature Review.

Journal: Cytogenetic and genome research

Published: January 25, 2016

Clinicopathologic study of primary renal hemangioblastoma

Journal: Zhonghua bing li xue za zhi = Chinese journal of pathology

Published: December 26, 2015

3p Deletion Syndrome Latest Advances

Find the Latest Research About 3p Deletion Syndrome

Missegregation of Chromosome 3 and Generation of Monosomy 3 in the Proliferating Uveal Melanoma Cells Under Hyperglycemia.

Missegregation of Chromosome 3 and Generation of Monosomy 3 in the Proliferating Uveal Melanoma Cells Under Hyperglycemia.

BAP1 Loss on Immunocytochemistry and Its Association With Monosomy 3 in Uveal Melanoma Fine-Needle Aspirations.

BAP1 Loss on Immunocytochemistry and Its Association With Monosomy 3 in Uveal Melanoma Fine-Needle Aspirations.

Lacrimal drainage anomalies in 3p deletion syndrome.

Lacrimal drainage anomalies in 3p deletion syndrome.

Adapted whole-body surveillance for von Hippel-Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report.

Adapted whole-body surveillance for von Hippel-Lindau-associated tumors in 3p deletion syndrome with VHL deletion: A case report.

Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements.

Fetal Cystic Hygroma Associated with Terminal 2p25.1 Duplication and Terminal 3p25.3 Deletion: Cytogenetic, Fluorescent in Situ Hybridization and Microarray Familial Characterization of Two Different Chromosomal Structural Rearrangements.

Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy.

Monosomy 3 Influences Epithelial-Mesenchymal Transition Gene Expression in Uveal Melanoma Patients; Consequences for Liquid Biopsy.

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.

Neuronal migration genes and a familial translocation t (3;17): candidate genes implicated in the phenotype.

Schizophrenia and epilepsy as a result of maternally inherited CNTN6 copy number variant.

Schizophrenia and epilepsy as a result of maternally inherited CNTN6 copy number variant.

Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma.

Prognostic value of chromosomal imbalances, gene mutations, and BAP1 expression in uveal melanoma.

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).

Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3→pter) and partial trisomy 16q (16q23.1→qter).

Chromosome r(3)(p25.3q29) in a Patient with Developmental Delay and Congenital Heart Defects: A Case Report and a Brief Literature Review.

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

Clinicopathologic study of primary renal hemangioblastoma