• 11p15 duplication and 13q34 deletion with Beckwith-Wiedemann syndrome and factor VII deficiency
• 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay
• A Case of a Lymphoplasmacytic Lymphoma with Trisomy 12 in the Lymphoid Population and Deletion 13q in the Unstimulated Cell Culture
• A large fraction of trisomy 12, 17p^-, and 11q^- CLL cases carry unidentified microdeletions of <em>miR-15a/16-1</em>
• A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia
• A rare unbalanced translocation (trisomy 5q33.3-qter, monosomy 13q34-qter) results in growth hormone deficiency and brain anomalies
• Abnormal FISH in patients with immunoglobulin light chain amyloidosis is a risk factor for cardiac involvement and for death
• AL amyloidosis: The effect of fluorescent in situ hybridization abnormalities on organ involvement and survival
• An unusual case of chronic lymphocytic leukemia with trisomy 12 and t(14;18) and a favorable response to ibrutinib
• Burden of cytogenetically abnormal plasma cells in light chain amyloidosis and their prognostic relevance
• Case Report: Prenatal Identification of a <em>De Novo</em> Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl
• CD49d shows superior performance characteristics for flow cytometric prognostic testing in chronic lymphocytic leukemia/small lymphocytic lymphoma
• Characterizing patients with multiple chromosomal aberrations detected by FISH in chronic lymphocytic leukemia
• Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenström's macroglobulinemia
• Chromosomal abnormalities by conventional cytogenetics and interphase fluorescence in situ hybridization in chronic lymphocytic leukemia in Taiwan, an area with low incidence--clinical implication and comparison between the West and the East
• Chromosomal alterations among age-related haematopoietic clones in Japan
• Chromosome analysis using spectral karyotyping (SKY)
• Chronic lymphocytic leukemia with t(14 ;18) and trisomy 12: a case report
• Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization
• Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population
• Clinico-pathological impact of cytogenetic subgroups in B-cell chronic lymphocytic leukemia: experience from India
• Combining cytogenetic and epigenetic approaches in chronic lymphocytic leukemia improves prognosis prediction for patients with isolated 13q deletion
• Concurrent rearrangements of BCL2, BCL3, and BCL11A genes in atypical chronic lymphocytic leukemia
• Constitutive activation of NF-κB signaling by NOTCH1 mutations in chronic lymphocytic leukemia
• Cytogenetic Abnormalities in Multiple Myeloma Patients at a Tertiary Healthcare Center in India
• Cytogenetic and molecular genetic diagnosis of a neonate with partial 13q trisomy and partial 5p monosomy
• Cytogenetic characteristics of B cell chronic lymphocytic leukemia in 275 Chinese patients by fluorescence in situ hybridization: a multicenter study
• Cytogenetic studies and their prognostic contribution in 565 Chinese patients with primary myelofibrosis
• Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
• Detection of genomic abnormalities among 105 patients with chronic lymphocytic leukemia using fluorescence in situ hybridization
• Distinct immunoglobulin heavy chain variable region gene repertoire and lower frequency of del(11q) in Taiwanese patients with chronic lymphocytic leukaemia
• Duplication of the ZIC2 gene is not associated with holoprosencephaly
• Employment of oligodeoxynucleotide plus interleukin-2 improves cytogenetic analysis in splenic marginal zone lymphoma
• Exploring the genetic landscape in chronic lymphocytic leukemia using high-resolution technologies
• External Quality Assessment for Detection of Fetal Trisomy 21, 18, and 13 by Massively Parallel Sequencing in Clinical Laboratories
• First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array
• Fluorescence in Situ Hybridization for Detecting Molecular Cytogenetic Abnormalities of Chronic Lymphocytic Leukemia
• Frequency and prognostic impact of the aberrant CD8 expression in 5,523 patients with chronic lymphocytic leukemia
• Gene mutations connected to Waldenstöm macroglobulinemia
• General population low-count CLL-like MBL persists over time without clinical progression, although carrying the same cytogenetic abnormalities of CLL
• Genetic abnormalities in chronic lymphocytic leukemia: where we are and where we go
• Genetic differences between Asian and Caucasian chronic lymphocytic leukemia
• Genomic alterations in chronic lymphocytic leukemia and their correlation with clinico-hematological parameters and disease progression
• Genomic characterisation of multiple myeloma: study of a Portuguese cohort
• Hexasomy 13q31.3q34 due to two marker chromosomes with inverted duplication in a fetus with increased nuchal translucency
• Hyperhaploidy is a novel high-risk cytogenetic subgroup in multiple myeloma
• Ibrutinib Treatment for First-Line and Relapsed/Refractory Chronic Lymphocytic Leukemia: Final Analysis of the Pivotal Phase Ib/II PCYC-1102 Study
• Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview
• Impact of primary molecular cytogenetic abnormalities and risk of progression in smoldering multiple myeloma
• Interphase fluorescence in situ hybridization in untreated AL amyloidosis has an independent prognostic impact by abnormality type and treatment category
• Intratumoral genetic heterogeneity and number of cytogenetic aberrations provide additional prognostic significance in chronic lymphocytic leukemia
• Jumping translocation involving chromosome 13q in a patient with Crohn's Disease and inv(16)(p13.1q22)/CBFB-MYH11 acute myeloid leukemia
• Jumping-like translocation-a rare chromosomal rearrangement in a patient with Burkitt lymphoma/leukemia
• Microarray analysis in fetuses with duodenal obstruction: It is not just trisomy 21
• microRNAome expression in chronic lymphocytic leukemia: comparison with normal B-cell subsets and correlations with prognostic and clinical parameters
• Mild phenotype of a large partial 13q trisomy
• Molecular and cytogenetic evaluation of a patient with ring chromosome 13 and discordant results
• Molecular basis of Waldenström macroglobulinemia
• Molecular cytogenetic detection of partial chromosome 13q trisomy and its relation with the clinical features of tortilcollis
• Molecular inversion probe array for the genetic evaluation of stillbirth using formalin-fixed, paraffin-embedded tissue
• Monoallelic and biallelic deletions of 13q14.3 in chronic lymphocytic leukemia: FISH vs miRNA RT-qPCR detection
• Monoclonal B-cell lymphocytosis is closely related to chronic lymphocytic leukaemia and may be better classified as early-stage CLL
• Mosaic proximal trisomy 13q and regular trisomy 13 in a female patient with long survival: Involvement of an incomplete trisomic rescue and a chromothripsis event
• Moyamoya syndrome secondary to mitochondrial disease in a patient with partial trisomy 13q14 and 13q31: A novel case report and literature review
• Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working group
• NOTCH1 mutations in +12 chronic lymphocytic leukemia (CLL) confer an unfavorable prognosis, induce a distinctive transcriptional profiling and refine the intermediate prognosis of +12 CLL
• Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature
• Novel recurrent chromosomal aberrations detected in clonal plasma cells of light chain amyloidosis patients show potential adverse prognostic effect: first results from a genome-wide copy number array analysis
• Partial duplication of 13q31.3-q34 and deletion of 13q34 associated with diaphragmatic hernia as a sole malformation in a fetus
• Partial monosomy 13q (13q21.32---&gt;qter) and partial trisomy 8p (8p1---&gt;pter) presenting with anencephaly and increased nuchal translucency: array comparative genomic hybridization characterization
• Partial trisomy 10p12.33 and partial monosomy 13q32.1: case report and a literature review
• Partial trisomy 13q in a blind and deaf baby boy
• Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy
• PARTIAL TRISOMY 4p AND PARTIAL MONOSOMY 13q: CASE REPORT AND A LITERATURE REVIEW
• Partial trisomy 7q and monosomy 13q in a child with disorder of sex development: phenotypic and genotypic findings
• Partial Trisomy of Chromosome 13 with a Novel Translocation (8 ; 13) and Unique Clinical Presentation in a Palestinian Infant
• Patients with Fanconi anemia and AML have different cytogenetic clones than de novo cases of AML
• Patterns of genomic aberrations suggest that Burkitt lymphomas with complex karyotype are distinct from other aggressive B-cell lymphomas with MYC rearrangement
• Phylloid hypomelanosis associated with a mosaic trisomy 13 in the 13q31.3-qter region: atypical phylloid distribution and typical hypomelanosis
• Precision diagnostics in chronic lymphocytic leukemia: Past, present and future
• Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation
• Prenatal Sonographic Features of Rare Chromosome 13 Aberrations
• Proliferation centers in chronic lymphocytic leukemia: correlation with cytogenetic and clinicobiological features in consecutive patients analyzed on tissue microarrays
• Real-world clinical experience in the Connect^® chronic lymphocytic leukaemia registry: a prospective cohort study of 1494 patients across 199 US centres
• Recent advances in trigonocephaly
• Recurrent Chromosomal Abnormalities in Tissues Involved by Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
• Recurrent chromosome abnormalities define nonoverlapping unique subgroups of tumors in patients with chronic lymphocytic leukemia and known karyotypic abnormalities
• Revised cytogenetic risk stratification in primary myelofibrosis: analysis based on 1002 informative patients
• Role of miR-15/16 in CLL
• RPPA-based proteomics recognizes distinct epigenetic signatures in chronic lymphocytic leukemia with clinical consequences
• Second cancers and Richter transformation are the leading causes of death in patients with trisomy 12 chronic lymphocytic leukemia
• Sequential karyotyping in Burkitt lymphoma reveals a linear clonal evolution with increase in karyotype complexity and a high frequency of recurrent secondary aberrations
• Study on prognostic significances of different cytogenetic risk categories in patients with primary myelodysplastic syndromes
• Subtype Distribution, Clinical Features, and Survival in B-cell Chronic Lymphoproliferative Disorders in China: A Review of 1592 Cases
• Telomere length and telomerase levels delineate subgroups of B-cell chronic lymphocytic leukemia with different biological characteristics and clinical outcomes
• The Dohner fluorescence in situ hybridization prognostic classification of chronic lymphocytic leukaemia (CLL): the CLL Research Consortium experience
• The morphology of CLL revisited: the clinical significance of prolymphocytes and correlations with prognostic/molecular markers in the LRF CLL4 trial
• The t(8;14)(q24.1;q32) and its variant translocations: A study of 34 cases
• Transient Plasmacytosis With Trisomy of Chromosome 8 in a Patient With Multiple Myeloma: A Case Report
• Trisomy 12 chronic lymphocytic leukemia expresses a unique set of activated and targetable pathways