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- 2010
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Mark
Genetic analysis of dasatinib-treated chronic myeloid leukemia rapidly developing into acute myeloid leukemia with monosomy 7 in Philadelphia-negative cells.
(
- Contribution to journal › Article
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Mark
Genetic profiles of gastroesophageal cancer: combined analysis using expression array and tiling array-comparative genomic hybridization
(
- Contribution to journal › Article
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Mark
Fusion of the FUS and CREB3L2 genes in a supernumerary ring chromosome in low-grade fibromyxoid sarcoma.
(
- Contribution to journal › Article
- 2009
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Mark
Clonal chromosome aberrations in a sialoblastoma
(
- Contribution to journal › Letter
- 2008
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Mark
Fusion of the COL1A1 and USP6 genes in a benign bone tumor.
(
- Contribution to journal › Article
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Mark
An endometrial stromal sarcoma cell line with the JAZF1/PHF1 chimera
(
- Contribution to journal › Article
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Mark
Cytogenetic and molecular cytogenetic findings in lipoblastoma.
(
- Contribution to journal › Article
- 2007
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Mark
Unstable translocation (8;22) in a case of giant cell reparative granuloma.
(
- Contribution to journal › Article
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Mark
Cytogenetic characterization and gene expression profiling of the trastuzumab-resistant breast cancer cell line JIMT-1.
(
- Contribution to journal › Article
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Mark
Comparison of the proximal promoter regions of the PAX3 and PAX7 genes
(
- Contribution to journal › Article
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Mark
Cytogenetic findings in pediatric renal cell carcinoma
(
- Contribution to journal › Article
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Mark
Tiling resolution array comparative genomic hybridization analysis of a fibrosarcoma of bone.
(
- Contribution to journal › Article
- 2006
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Mark
Array-based comparative genomic hybridization characterization of cytogenetically polyclonal myeloid malignancies.
(
- Contribution to journal › Letter
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Mark
Cytogenetic aberrations in immortalization of esophageal epithelial cells
(
- Contribution to journal › Article
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Mark
Cytogenetic abnormalities in 106 oral squamous cell carcinomas
(
- Contribution to journal › Article
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Mark
Chromosome aberrations including der(6)t(2;6)(p15;p21.3) and der(22)t(3;22)(p21;p11) in the evolution of essential thrombocythemia to myelofibrosis with myeloid metaplasia
(
- Contribution to journal › Article
- 2005
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Mark
Absence of mutations of the BRAF gene in malignant melanoma of soft parts (clear cell sarcoma of tendons and aponeuroses)
(
- Contribution to journal › Article
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Mark
Defective mismatch-repair as a minor tumorigenic pathway in Barrett esophagus-associated adenocarcinoma.
(
- Contribution to journal › Article
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Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
(
- Contribution to journal › Article
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Mark
Immortalization of human extravillous cytotrophoblasts by human papilloma virus gene E6E7: sequential cytogenetic and molecular genetic characterization.
(
- Contribution to journal › Article
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Mark
Karyotypic evolution and tumor progression in head and neck squamous cell carcinomas.
(
- Contribution to journal › Article
- 2004
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Mark
Combined binary ratio labeling fluorescence in situ hybridization analysis of chordoma
(
- Contribution to journal › Article
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Mark
Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.
(
- Contribution to journal › Article
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Mark
Statistical dissection of cytogenetic patterns in lung cancer reveals multiple modes of karyotypic evolution independent of histological classification.
(
- Contribution to journal › Article
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Mark
Sequential cytogenetic and molecular cytogenetic characterization of an SV40T-immortalized nasopharyngeal cell line transformed by Epstein-Barr virus latent membrane protein-1 gene
(
- Contribution to journal › Article
-
Mark
Statistical analyses of karyotypic complexity in head and neck squamous cell carcinoma.
(
- Contribution to journal › Article
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Mark
Wilms tumors develop through two distinct karyotypic pathways.
(
- Contribution to journal › Article
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Mark
Cytogenetic and fluorescence in situ hybridization characterization of clonal chromosomal aberrations and CCND1 amplification in esophageal carcinomas
(
- Contribution to journal › Article
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Mark
Different gene expression in immunoglobulin-mutated and immunoglobulin-unmutated forms of chronic lymphocytic leukemia.
(
- Contribution to journal › Article
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Mark
A novel t(2;17) in transformation of essential thrombocythemia to acute myelocytic leukemia
(
- Contribution to journal › Article
- 2003
-
Mark
Comparative cytogenetic and DNA flow cytometric analysis of 242 primary breast carcinomas
(
- Contribution to journal › Article
-
Mark
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies. a multicolor and locus-specific fluorescence in situ hybridization study.
(
- Contribution to journal › Article
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Mark
Chromosomal abnormalities in inflammatory pseudotumor of the urinary bladder
(
- Contribution to journal › Article
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Mark
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors
(
- Contribution to journal › Article
-
Mark
Cytogenetic and molecular genetic analyses of endometrial stromal sarcoma: nonrandom involvement of chromosome arms 6p and 7p and confirmation of JAZF1/JJAZ1 gene fusion in t(7;17)
(
- Contribution to journal › Article
-
Mark
Changes in apoptosis-related pathways in acute myelocytic leukemia.
(
- Contribution to journal › Article
- 2002
-
Mark
Fluorescence in situ hybridization for the study of cell lineage involvement in myelodysplastic syndromes with chromosome 5 anomalies
(
- Contribution to journal › Article
-
Mark
Cytogenetic abnormalities in a hemangiopericytoma of the spleen.
(
- Contribution to journal › Article
-
Mark
Coping with complexity. multivariate analysis of tumor karyotypes.
(
- Contribution to journal › Article
-
Mark
Cytogenetic aberrations and heterogeneity of mutations in repeat-containing genes in a colon carcinoma from a patient with hereditary nonpolyposis colorectal cancer.
(
- Contribution to journal › Article
-
Mark
Karyotypic heterogeneity and clonal evolution in squamous cell carcinomas of the head and neck.
(
- Contribution to journal › Article
-
Mark
Clonal chromosome abnormalities in premalignant lesions of the skin.
(
- Contribution to journal › Article
-
Mark
Refractory anemia with ring sideroblasts associated with i(17q) and mutation of the TP53 gene
(
- Contribution to journal › Article
- 2001
-
Mark
Analysis of the distribution and frequency of trisomy 7 in vivo in synovia from patients with osteoarthritis and pigmented villonodular synovitis
(
- Contribution to journal › Article
-
Mark
The incidence of trisomy 8 as a sole chromosomal aberration in myeloid malignancies varies in relation to gender, age, prior iatrogenic genotoxic exposure, and morphology
(
- Contribution to journal › Article
-
Mark
Cytogenetic and fluorescence in situ hybridization characterization of chromosome 8 rearrangements in head and neck squamous cell carcinomas
(
- Contribution to journal › Article
-
Mark
Extensive cytogenetic heterogeneity in a benign retroperitoneal schwannoma
(
- Contribution to journal › Article
- 2000
-
Mark
Radiation-associated sarcomas are characterized by complex karyotypes with frequent rearrangements of chromosome arm 3p
(
- Contribution to journal › Article
-
Mark
Cytogenetic heterogeneity and clonal evolution in synchronous bilateral breast carcinomas and their lymph node metastases from a male patient without any detectable BRCA2 germline mutation
(
- Contribution to journal › Article
- 1998
-
Mark
Amplification of 12q13 and 12q15 sequences in a sclerosing epithelioid fibrosarcoma
(
- Contribution to journal › Article
- 1997
-
Mark
Monosomy 22 in a case of biliary adenofibroma
(
- Contribution to journal › Article
- 1992
-
Mark
Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia
(
- Contribution to journal › Article
- 1991
-
Mark
New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
- 1990
-
Mark
Complex karyotypic changes, including rearrangements of 12q13 and 14q24, in two leiomyosarcomas
(
- Contribution to journal › Article
-
Mark
Localization of the chromosomal breakpoints of the t(12;16) in liposarcoma to subbands 12q13.3 and 16p11.2
(
- Contribution to journal › Article
- 1988
-
Mark
Do clonal chromosome abnormalities prognosticate early relapse in hodgkin's disease?
(
- Contribution to journal › Letter
-
Mark
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma
(
- Contribution to journal › Article
- 1987
-
Mark
Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma
(
- Contribution to journal › Article
- 1986
-
Mark
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
-
Mark
Near-haploidy in a case of plasmocytoma
(
- Contribution to journal › Article
- 1985
-
Mark
C-band heteromorphism in breast cancer patients
(
- Contribution to journal › Article