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- 2003
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Mark
Fusion of the NUP98 gene and the homeobox gene HOXC13 in acute myeloid leukemia with t(11;12)(p15;q13).
(
- Contribution to journal › Article
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Mark
Provision of genetic service in Europe: current practices and issues.
(
- Contribution to journal › Article
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Mark
A novel chromosomal translocation t(3;7)(q26;q21) in myeloid leukemia resulting in overexpression of EVI1
(
- Contribution to journal › Published meeting abstract
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Mark
A novel fusion gene, SS18L1/SSX1, in synovial sarcoma
(
- Contribution to journal › Article
-
Mark
Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non-mosaic patients?
(
- Contribution to journal › Letter
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Mark
A pooled analysis of karyotypic patterns, breakpoints and imbalances in 783 cytogenetically abnormal multiple myelomas reveals frequently involved chromosome segments as well as significant age- and sex-related differences.
(
- Contribution to journal › Article
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Mark
Consequences of eliminating adenosine A(1) receptors in mice
(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
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Mark
Data storage and DNA banking for biomedical research: technical, social and ethical issues.
(
- Contribution to journal › Article
- 2002
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Mark
Prognostically important chromosomal aberrations in soft tissue sarcomas: a report of the Chromosomes and Morphology (CHAMP) Study Group.
(
- Contribution to journal › Article
-
Mark
Fusion of RDC1 with HMGA2 in lipomas as the result of chromosome aberrations involving 2q35-37 and 12q13-15.
(
- Contribution to journal › Article