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- 2006
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Mark
Identification of cryptic aberrations and characterization of translocation breakpoints using array CGH in high hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
- 2005
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Mark
The parental origin of trisomy 14 in hyperdiploid childhood ALL
(
- Contribution to journal › Letter
-
Mark
Formation of der(19)t(1;19)(q23;p13) in acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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Mark
Evidence for a single-step mechanism in the origin of hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
-
Mark
Trisomies in Hematologic Malignancies
2005) In Lund University Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
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Mark
Multicolor fluorescence in situ hybridization characterization of cytogenetically polyclonal hematologic malignancies.
(
- Contribution to journal › Article
- 2004
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Mark
Identification of a commonly amplified 4.3 Mb region with overexpression of the C8FW gene, encoding a phosphoprotein regulated by mitogenic pathways, but not of the MYC gene in MYC-containing double minutes in myeloid malignancies.
(
- Contribution to journal › Article
- 2003
-
Mark
Formation of trisomies and their parental origin in hyperdiploid childhood acute lymphoblastic leukemia.
(
- Contribution to journal › Article
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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
-
Mark
MYC is not overexpressed in a case of chronic myelomonocytic leukemia with MYC-containing double minutes
(
- Contribution to journal › Letter