Cancer Genetics and Cytogenetics Journal

The t(6;9)(p22;q34) in myeloid neoplasms: a retrospective study of 16 cases

Fulltext Access 6 Pages 2010

6p21 rearrangements in uterine leiomyomas targeting HMGA1

Fulltext Access 6 Pages 2010

Urine from current smokers induces centrosome aberrations and spindle defects in vitro in nonmalignant human cell lines

Fulltext Access 10 Pages 2010

Role of TP53 Arg72Pro polymorphism in urinary bladder cancer predisposition and predictive impact of proline related genotype in advanced tumors in an ethnic Kashmiri population

Fulltext Access 6 Pages 2010

Correlation between clinical characteristics, survival and genetic alterations in patients with hepatocellular carcinoma from Saudi Arabia

Fulltext Access 9 Pages 2010

FISH-negative cryptic PML–RARA rearrangement detected by long-distance polymerase chain reaction and sequencing analyses: a case study and review of the literature

Fulltext Access 6 Pages 2010

B lymphoblastic leukemia with ETV6 amplification

Fulltext Access 4 Pages 2010

Therapy-related acute myeloid leukemia with t(2;11)(q37;q23) after treatment for osteosarcoma

Fulltext Access 4 Pages 2010

FLT3-internal tandem duplication in a pediatric patient with t(8;21) acute myeloid leukemia

Fulltext Access 5 Pages 2010

Evaluation of upper urinary tract tumors by FISH in Chinese patients

Fulltext Access 9 Pages 2010

Three rearrangements of chromosome 5 in a patient with myelodysplastic syndrome: an atypical deletion 5q, a complex intrachromosomal rearrangement of chromosome 5, and a paracentric inversion of chromosome 5

Fulltext Access 6 Pages 2010

Chromosomal alterations in Malaysian patients with nasopharyngeal carcinoma analyzed by comparative genomic hybridization

Fulltext Access 4 Pages 2010

Screening for common copy-number variants in cancer genes

Fulltext Access 8 Pages 2010

Screening for DNA copy number aberrations in mucinous adenocarcinoma arising from the minor salivary gland: two case reports

Fulltext Access 4 Pages 2010

Translocation (3;8)(q27;q24) in two cases of triple hit lymphoma

Fulltext Access 5 Pages 2010

A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia

Fulltext Access 8 Pages 2010

Chromosomal imbalances in urinary bladder paraganglioma

Fulltext Access 4 Pages 2010

A case of acute myeloid leukemia initially treated as chronic lymphocytic leukemia: what do we know about t(4;12)(q12;p13)?

Fulltext Access 4 Pages 2010

Numerical chromosomal changes and risk of development of myelodysplastic syndrome–acute myeloid leukemia in patients with Fanconi anemia

Fulltext Access 7 Pages 2010

Cytogenetics and genetics of human cancer: methods and accomplishments

Fulltext Access 25 Pages 2010

MicroRNA in chronic lymphocytic leukemia: transitioning from laboratory-based investigation to clinical application

Fulltext Access 7 Pages 2010

Stimulation of chronic lymphocytic leukemia cells with CpG oligodeoxynucleotide gives consistent karyotypic results among laboratories: a CLL Research Consortium (CRC) Study

Fulltext Access 7 Pages 2010

Standardization of fluorescence in situ hybridization studies on chronic lymphocytic leukemia (CLL) blood and marrow cells by the CLL Research Consortium

Fulltext Access 8 Pages 2010

Gene dosage effects in chronic lymphocytic leukemia

Fulltext Access 12 Pages 2010

Progressive but previously untreated CLL patients with greater array CGH complexity exhibit a less durable response to chemoimmunotherapy

Fulltext Access 8 Pages 2010

Correlation of cytomorphology, immunophenotyping, and interphase fluorescence in situ hybridization in 381 patients with monoclonal gammopathy of undetermined significance and 301 patients with plasma cell myeloma

Fulltext Access 7 Pages 2010

Examination of copy number variations of CHST9 in multiple types of hematologic malignancies

Fulltext Access 4 Pages 2010

Table of Contents

Fulltext Access 4 Pages 2010

Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review

Fulltext Access 6 Pages 2010

Cytogenetic features of 5q deletion and 5q− syndrome in myelodysplastic syndrome in Korea; marker chromosomes proved to be chromosome 5 with interstitial deletion by fluorescence in situ hybridization

Fulltext Access 10 Pages 2010

Human fetal/tumor metakaryotic stem cells: pangenomic homologous pairing and telomeric end-joining of chromatids

Fulltext Access 6 Pages 2010

Clonal heterogeneity and chromosomal instability at disease presentation in high hyperdiploid acute lymphoblastic leukemia

Fulltext Access 6 Pages 2010

GSTT1 copy number gain is a poor predictive marker for escalated-dose imatinib treatment in chronic myeloid leukemia: genetic predictive marker found using array comparative genomic hybridization

Fulltext Access 7 Pages 2010

EGFR expression and gene copy number in triple-negative breast carcinoma

Fulltext Access 8 Pages 2010

Germline mutations of BRCA1 and BRCA2 genes in Turkish breast, ovarian, and prostate cancer patients

Fulltext Access 8 Pages 2010