Mattias Höglund
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- 1999
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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
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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
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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
- 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
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- Contribution to journal › Article
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Mark
ETV6/ABL fusion is rare in Ph-negative chronic myeloid disorders
(
- 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
- 1997
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Mark
BCR/ABL-negative chronic myeloid leukemia with ETV6/ABL fusion
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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
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- 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