• <em>De novo</em> 3q13.13q21.2 interstitial deletion and paternal 12p13.3 microdeletion in a fetus with dysplasia of the corpus callosum and ventriculomegaly: A case report
• "T-cell prolymphocytic leukemia (T-PLL), a heterogeneous disease exemplified by two cases and the important role of cytogenetics: a multidisciplinary approach"
• 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
• A 10.46 Mb 12p11.1-12.1 interstitial deletion coincident with a 0.19 Mb NRXN1 deletion detected by array CGH in a girl with scoliosis and autism
• A 4.5 Mb terminal deletion of chromosome 12p helps further define a psychosis-associated locus
• A compendium of myeloma-associated chromosomal copy number abnormalities and their prognostic value
• A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia
• A Comprehensive Update on Molecular and Cytogenetic Abnormalities in T-cell Prolymphocytic Leukemia (T-pll)
• A molecular portrait of gastrointestinal stromal tumors: an integrative analysis of gene expression profiling and high-resolution genomic copy number
• A Novel Assay for the Identification of NOTCH1 PEST Domain Mutations in Chronic Lymphocytic Leukemia
• An unusual child case of myeloid/natural killer cell precursor acute leukemia treated successfully with acute myeloid leukemia-oriented chemotherapy
• Analysis of chromosomal abnormalities in pancreatic cancer by spectral karyotyping
• Analysis of chromosome 12p deletion in plasma cell dyscrasias
• Analysis of copy number variations in an infant with Cri du Chat syndrome by array-based comparative genomic hybridization
• Array comparative genomic hybridization and sequencing of 23 genes in 80 patients with myelofibrosis at chronic or acute phase
• Array comparative genomic hybridization reveals frequent alterations of G1/S checkpoint genes in undifferentiated pleomorphic sarcoma of bone
• Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12
• Bifocal germinoma in a patient with 16p11.2 microdeletion syndrome
• CACNA1C haploinsufficiency accounts for the common features of interstitial 12p13.33 deletion carriers
• CDKN1B, encoding the cyclin-dependent kinase inhibitor 1B (p27), is located in the minimally deleted region of 12p abnormalities in myeloid malignancies and its low expression is a favorable prognostic marker in acute myeloid leukemia
• Cecum perforation in intestinal malrotation setting in a patient with chromosome 12p deletion syndrome: A case report
• Characterization of a rare mosaic unbalanced translocation of t(3;12) in a patient with neurodevelopmental disorders
• Characterization of pancreatic ductal adenocarcinoma using whole transcriptome sequencing and copy number analysis by single-nucleotide polymorphism array
• Chromosomal Aberrations in ETV6/RUNX1-positive Childhood Acute Lymphoblastic Leukemia using 244K Oligonucleotide Array Comparative Genomic Hybridization
• Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case
• Chromosome 12p Amplification in Triple-Negative/<em>BRCA1-</em>Mutated Breast Cancer Associates with Emergence of Docetaxel Resistance and Carboplatin Sensitivity
• Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype: A Case Report and Review of Literature
• Chromosome 3 anomalies investigated by genome wide SNP analysis of benign, low malignant potential and low grade ovarian serous tumours
• Chromosome microarray characterisation of chromosome arm 12p loss associated with complex molecular karyotype and recurrent adverse cytogenetic markers in multiple myeloma
• Chronic lymphocytic leukemia with a FGFR3 translocation: case report and literature review of an uncommon cytogenetic event
• Clinical and Cytogenetic Characteristics of Two AML Patients with High-level MLL Expression
• Clinical value of genetic analysis in prenatal diagnosis of short femur
• Concurrent Loss of Heterozygosity and Mosaic Deletion of 12p13.32pter
• Copy Number Alterations Associated with Acute Lymphoblastic Leukemia in Mexican Children. A report from The Mexican Inter-Institutional Group for the identification of the causes of childhood leukemia
• Copy number genome alterations are associated with treatment response and outcome in relapsed childhood ETV6/RUNX1-positive acute lymphoblastic leukemia
• Copy number variation in plasma as a tool for lung cancer prediction using Extreme Gradient Boosting (XGBoost) classifier
• Copy-neutral loss of heterozygosity and chromosome gains and losses are frequent in gastrointestinal stromal tumors
• Correction: Genomic deletion of chromosome 12p is an independent prognostic marker in prostate cancer
• Cytogenetic abnormalities predict treatment-free interval and response to therapy in previously untreated chronic lymphocytic leukemia patients
• Cytogenetic and genetic pathways in therapy-related acute myeloid leukemia
• Cytogenomic Analysis of Long-Term Epilepsy-Associated Tumors Using an Array-Based CGH Strategy
• Deciphering the molecular genetic basis of NPC through molecular, cytogenetic, and epigenetic approaches
• Deletion 12p12 involving SOX5 in two children with developmental delay and dysmorphic features
• Deletion of GOLGA2P3Y but not GOLGA2P2Y is a risk factor for oligozoospermia
• Detection of deletions and/or amplifications of genes related with lung cancer by multiplex ligation-dependent probe amplification (MLPA) technique
• Duplication 9p and their implication to phenotype
• Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome
• Frequency of del(12p) is commonly underestimated in myelodysplastic syndromes: Results from a German diagnostic study in comparison with an international control group
• Frequent chromatin rearrangements in myelodysplastic syndromes--what stands behind?
• Frequent deletion of CDKN2A and recurrent coamplification of KIT, PDGFRA, and KDR in fibrosarcoma of bone--an array comparative genomic hybridization study
• Genetic abnormalities in chronic lymphocytic leukemia: where we are and where we go
• Genetic changes observed in a case of adult pilocytic astrocytoma revealed by array CGH analysis
• Genetic prognostic factors in childhood acute myeloid leukemia
• Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events
• Genomic deletion of chromosome 12p is an independent prognostic marker in prostate cancer
• Genomic evolution and chemoresistance in germ-cell tumours
• Genomic imbalances in esophageal squamous cell carcinoma identified by molecular cytogenetic techniques
• Genomic landscape of <em>TP53</em> -mutated myeloid malignancies
• Genotype-phenotype relationship in a child with 2.3 Mb de novo interstitial 12p13.33-p13.32 deletion
• Heterogeneity in the prognostic significance of 12p deletion and chromosome 5 amplification in multiple myeloma
• Heterogeneous chromosome 12p deletion is an independent adverse prognostic factor and resistant to bortezomib-based therapy in multiple myeloma
• High frequency of BTG1 deletions in acute lymphoblastic leukemia in children with down syndrome
• Hypodiploid multiple myeloma is characterized by more aggressive molecular markers than non-hyperdiploid multiple myeloma
• Identification of genetic parameters associated with disease progression in plasma cell myeloma
• Importance of FISH combined with Morphology, Immunophenotype and Cytogenetic Analysis of Childhood/ Adult Acute Lymphoblastic Leukemia in Omani Patients
• Inherited 5p deletion syndrome due to paternal balanced translocation: Phenotypic heterogeneity due to duplication of 8q and 12p
• Interaction between 12p chromosomal abnormalities and Lnc-HOTAIR mediated pathway in acute myeloid leukemia
• Interstitial 12p deletion involving more than 40 genes in a patient with postnatal microcephaly, psychomotor delay, optic nerve atrophy, and facial dysmorphism
• Karyotype and chromosome variability in the armadillo Chaetophractus villosus in Argentina
• Malignant teratoma of the thyroid: A difficult diagnosis by fine-needle aspiration
• Molecular correlates of male germ cell tumors with overgrowth of components resembling somatic malignancies
• Molecular cytogenetic characterization and genotype/phenotype analysis in a patient with a de novo 8p23.2p23.3 deletion/12p13.31p13.33 duplication
• Monoclonal gammopathy and serum immunoglobulin levels as prognostic factors in chronic lymphocytic leukaemia
• Morphologic identification of atypical chronic lymphocytic leukemia by digital microscopy
• Next Generation Cytogenetics in Myeloid Hematological Neoplasms: Detection of CNVs and Translocations
• Novel clinically relevant genes in gastrointestinal stromal tumors identified by exome sequencing
• Orbital myeloid sarcoma in an adult with acute myeloid leukemia, FAB M1, and 12p-deletion
• Papillary haemangioma in the spinal canal of a patient with a germline 12p microdeletion
• 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
• Prognostic significance of copy-number alterations in multiple myeloma
• Prognostic significance of cytogenetic abnormalities in T-cell prolymphocytic leukemia
• PTEN nuclear translocation enhances neuronal injury after hypoxia-ischemia via modulation of the nuclear factor-κB signaling pathway
• Refractory T cell acute lymphoblastic leukemia with unusual karyotype and interesting immunophenotype
• Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports
• Secondary complex chromosome rearrangement identified by chromosome analysis and FISH subsequent to detection of an unbalanced derivative chromosome 12 by SNP array analysis
• Seminoma component of mixed testicular germ cell tumor shows a higher incidence of loss of heterozygosity than pure-type seminoma
• Simultaneous deletion of 3'ETV6 and 5'EWSR1 genes in blastic plasmacytoid dendritic cell neoplasm: case report and literature review
• Spontaneous Single-Copy Loss of TP53 in Human Embryonic Stem Cells Markedly Increases Cell Proliferation and Survival
• Submicroscopic subtelomeric aberrations in Chinese patients with unexplained developmental delay/mental retardation
• Subtelomeric deletion of 12p: Description of a third case and review
• Tensor GSVD of patient- and platform-matched tumor and normal DNA copy-number profiles uncovers chromosome arm-wide patterns of tumor-exclusive platform-consistent alterations encoding for cell transformation and predicting ovarian cancer survival
• The genetic landscape of 87 ovarian germ cell tumors
• The genetics of common disorders - congenital diaphragmatic hernia
• The genomic landscape of TP53 and p53 annotated high grade ovarian serous carcinomas from a defined founder population associated with patient outcome
• Third-Generation Cytogenetic Analysis: Diagnostic Application of Long-Read Sequencing
• Tripartite motif‑containing 11 regulates the proliferation and apoptosis of breast cancer cells
• 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
• Vulvar Yolk Sac Tumors Are Somatically Derived SMARCB1 (INI-1)-Deficient Neoplasms