Division of Clinical Genetics
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- 2004
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Mark
MLL/GRAF fusion in an infant acute monocytic leukemia (AML M5b) with a cytogenetically cryptic ins(5;11)(q31;q23q23).
(
- Contribution to journal › Article
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Mark
Clinical impact of internal tandem duplications and activating point mutations in FLT3 in acute myeloid leukemia in elderly patients.
(
- Contribution to journal › Article
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Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article
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Mark
Cytogenetic and molecular genetic characterization of immortalized human ovarian surface epithelial cell lines: consistent loss of chromosome 13 and amplification of chromosome 20
(
- Contribution to journal › Article
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Mark
Clinical and biological importance of cytogenetic abnormalities in childhood and adult acute lymphoblastic leukemia
(
- Contribution to journal › Scientific review
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Mark
High frequencies of chromosomal aberrations in multiple myeloma and monoclonal gammopathy of undetermined significance in direct chromosome preparation.
(
- Contribution to journal › Article
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Mark
Molecular genetic characterization of the genomic ACTB-GLI fusion in pericytoma with t(7;12).
(
- Contribution to journal › Article
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Mark
Characterization of Genetic Abnormalities at Disease Progression of Chronic Myeloid Leukemia
2004)(
- Thesis › Doctoral thesis (compilation)
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Mark
Genetic characterization of bone and soft tissue tumors
(
- Contribution to journal › Article
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Mark
Regulation of genetic testing in clinical practice
(
- Chapter in Book/Report/Conference proceeding › Book chapter