• A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation
• A 1.5Mb terminal deletion of 12p associated with autism spectrum disorder
• CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers
• Characterization of a rare mosaic unbalanced translocation of t(3;12) in a patient with neurodevelopmental disorders
• Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case
• Clinical and Cytogenetic Characteristics of Two AML Patients with High-level MLL Expression
• Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter
• Duplication 9p and their implication to phenotype
• Frequent chromatin rearrangements in myelodysplastic syndromes--what stands behind?
• Genotype-phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion
• Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication
• Partial trisomy 11q and partial monosomy 12p due to the maternal translocation (11q;12p)
• Prenatal diagnosis of the Dandy-Walker malformation associated with partial trisomy 12p and distal 15q deletion
• Simultaneous deletion of 3'ETV6 and 5'EWSR1 genes in blastic plasmacytoid dendritic cell neoplasm: case report and literature review
• Variable Phenotypes of Epilepsy, Intellectual Disability, and Schizophrenia Caused by 12p13.33-p13.32 Terminal Microdeletion in a Korean Family: A Case Report and Literature Review