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- 2006
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Mark
Truncation and fusion of HMGA2 in lipomas with rearrangements of 5q32-->q33 and 12q14-->q15.
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- Contribution to journal › Article
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Mark
Genomic profiling of bone and soft tissue tumors with supernumerary ring chromosomes using tiling resolution bacterial artificial chromosome microarrays.
(
- Contribution to journal › Article
- 2005
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Mark
Ewing tumours and synovial sarcomas have critical features of karyotype evolution in common with epithelial tumours.
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- Contribution to journal › Article
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Mark
Structural and numerical chromosome changes in colon cancer develop through telomere-mediated anaphase bridges, not through mitotic multipolarity.
(
- Contribution to journal › Article
- 2004
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Mark
Telomere shortening and mitotic dysfunction generate cytogenetic heterogeneity in a subgroup of renal cell carcinomas.
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- Contribution to journal › Article
- 2003
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Mark
Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors
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- Contribution to journal › Article
- 2002
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Mark
Differentially amplified chromosome 12 sequences in low- and high-grade osteosarcoma.
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- Contribution to journal › Article
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Mark
Molecular cytogenetic mapping of recurrent chromosomal breakpoints in tenosynovial giant cell tumors.
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- Contribution to journal › Article
- 2001
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Mark
Multivariate analyses of genomic imbalances in solid tumors reveal distinct and converging pathways of karyotypic evolution
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- Contribution to journal › Article
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Mark
Abnormal nuclear shape in solid tumors reflects mitotic instability
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- Contribution to journal › Article
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Mark
Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors
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- Contribution to journal › Article
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Mark
Identification of cytogenetic subgroups and karyotypic pathways in transitional cell carcinoma
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- Contribution to journal › Article
- 2000
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Mark
Locus-specific multifluor FISH analysis allows physical characterization of complex chromosome abnormalities in neoplasia
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- Contribution to journal › Article
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Mark
Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity
(
- Contribution to journal › Article
- 1999
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Mark
Unique cytological features and chromosome aberrations in chondroid lipoma: a case report based on fine-needle aspiration cytology, histopathology, electron microscopy, chromosome banding, and molecular cytogenetics
(
- Contribution to journal › Article
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Mark
Hibernomas are characterized by homozygous deletions in the multiple endocrine neoplasia type I region. Metaphase fluorescence in situ hybridization reveals complex rearrangements not detected by conventional cytogenetics
(
- Contribution to journal › Article
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Mark
Variable stability of chromosomes containing amplified alpha-satellite sequences in human mesenchymal tumours
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- Contribution to journal › Article
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Mark
The structure and dynamics of ring chromosomes in human neoplastic and non-neoplastic cells
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- Contribution to journal › Article
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Mark
Rearrangement of the neoplasia-associated gene HMGIC in synovia from patients with osteoarthritis
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- Contribution to journal › Article
- 1998
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Mark
Chromosomal organization of amplified chromosome 12 sequences in mesenchymal tumors detected by fluorescence in situ hybridization
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- Contribution to journal › Article
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Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article
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Mark
A case of dermatofibrosarcoma protuberans with a ring chromosome 5 and a rearranged chromosome 22 containing amplified COL1A1 and PDGFB sequences
(
- Contribution to journal › Article
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Mark
Polyclonal expansion of cells with trisomy 7 in synovia from patients with osteoarthritis
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- Contribution to journal › Article
- 1996
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Mark
Expression patterns of the human sarcoma-associated genes FUS and EWS and the genomic structure of FUS
(
- Contribution to journal › Article
- 1994
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Mark
Fusion of the FUS gene with ERG in acute myeloid leukemia with t(16;21)(p11;q22)
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- Contribution to journal › Article