Division of Clinical Genetics
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- 2006
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Mark
High incidence of the ETV6/RUNX1 fusion gene in paediatric precursor B-cell acute lymphoblastic leukaemias with trisomy 21 as the sole cytogenetic change: a Nordic series of cases diagnosed 1989-2005.
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- Contribution to journal › Article
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Mark
Comparison of ST-Segment Deviation to Scintigraphically Quantified Myocardial Ischemia During Acute Coronary Occlusion Induced by Percutaneous Transluminal Coronary Angioplasty.
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- Contribution to journal › Article
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Mark
Fusion of ETV6 with an intronic sequence of the BAZ2A gene in a paediatric pre-B acute lymphoblastic leukaemia with a cryptic chromosome 12 rearrangement.
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- Contribution to journal › Article
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Mark
Determination of the ability of high-frequency ECG to estimate left ventricular mass in humans, determined by magnetic resonance imaging.
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- Contribution to journal › Article
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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
Human short-term repopulating cells have enhanced telomerase reverse transcriptase expression.
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- Contribution to journal › Article
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Mark
Re: Wilting et al. Increased gene copy numbers at chromosome 20q are frequent in both squamous cell carcinomas and adenocarcinomas of the cervix. J Pathol 2006; 209:220-230.
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- Contribution to journal › Letter
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Mark
Education in medical genetics for non-genetic health care providers in sweden.
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- Contribution to journal › Article
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Mark
Molecular characterization of early-stage bladder carcinomas by expression profiles, FGFR3 mutation status, and loss of 9q.
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- Contribution to journal › Article
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Mark
MYC-containing double minutes in hematologic malignancies: evidence in favor of the episome model and exclusion of MYC as the target gene
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- Contribution to journal › Article