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- 2010
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Mark
Heterogeneous and Complex Rearragements of the Long Arm of Chromosome 6 in Chondromyxoid Fibroma
2010) 99th Annual Meeting of the United-States-and-Canadian-Academy-of-Pathology In Modern Pathology 23(Suppl. 1). p.27-27(
- Contribution to journal › Published meeting abstract
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Mark
Unrelated clones in AML/MDS - characterisation and prognostic relevance
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- Contribution to journal › Published meeting abstract
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Mark
Molecular and functional studies of ABL1 and FGFR1 fusion oncogenes in myeloproliferative neoplasms
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- Thesis › Doctoral thesis (compilation)
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Mark
A Human Model of IMO by Lentiviral Mediated shRNA Knock-down of Tcirg1 in CD34+Cells
2010) 18th Annual Congress of the European-Society-of-Gene-and-Cell-Therapy In Human Gene Therapy 21(10). p.1458-1459(
- Contribution to journal › Published meeting abstract
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Mark
NordicDB: a Nordic pool and portal for genome-wide control data
(
- Contribution to journal › Article
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Mark
A Missense Mutation in the Aggrecan C-type Lectin Domain Disrupts Extracellular Matrix Interactions and Causes Dominant Familial Osteochondritis Dissecans
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- Contribution to journal › Article
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Mark
How to Handle Genetic Information: A Comparison of Attitudes among Patients and the General Population
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- Contribution to journal › Article
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Mark
Altered expression and distribution of cathepsins in neuronopathic forms of Gaucher disease and in other sphingolipidoses
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- Contribution to journal › Article
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Mark
A point mutation in the dynein heavy chain gene leads to striatal atrophy and compromises neurite outgrowth of striatal neurons
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- Contribution to journal › Article
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Mark
The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of A beta in different brain regions
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- Contribution to journal › Article