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- 2010
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Mark
The correlation pattern of acquired copy number changes in 164 ETV6/RUNX1-positive childhood acute lymphoblastic leukemias
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- Contribution to journal › Article
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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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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 Laboratory Investigation 90(Suppl. 1). p.27-27(
- Contribution to journal › Published meeting abstract
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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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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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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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Integrative genomics identifies DSCR1 (RCAN1) as a novel NFAT-dependent mediator of phenotypic modulation in vascular smooth muscle cells
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- Contribution to journal › Article
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Molecular Analysis Expands the Spectrum of Phenotypes Associated with GLI3 Mutations
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- Contribution to journal › Article
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Differential Transduction Following Basal Ganglia Administration of Distinct Pseudotyped AAV Capsid Serotypes in Nonhuman Primates
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- Contribution to journal › Article
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Successful Treatment of Metachromatic Leukodystrophy Using Bone Marrow Transplantation of HoxB4 Overexpressing Cells
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- Contribution to journal › Article