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- 2008
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Mark
Mutations of FLT3, NRAS, KRAS, and PTPN11 are frequent and possibly mutually exclusive in high hyperdiploid childhood acute lymphoblastic leukemia
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- Contribution to journal › Article
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Mark
The Fatty Acid Amide Hydrolase (FAAH) Pro129Thr Polymorphism is not Associated with Severe Obesity in Greek Subjects
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- Contribution to journal › Article
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Mark
The FLT3 inhibitor PKC412 in combination with cytostatic drugs in vitro in acute myeloid leukemia
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- Contribution to journal › Article
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Mark
Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay.
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- Contribution to journal › Article
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Mark
Female haemophilia A caused by skewed X inactivation
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- Contribution to journal › Letter
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Mark
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survival
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- Contribution to journal › Article
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Mark
What is ideal genetic counselling? A survey of current international guidelines
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- Contribution to journal › Article
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Mark
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives
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- Contribution to journal › Article
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Mark
Tissue microarray based analysis of prognostic markers in invasive bladder cancer: Much effort to no avail?
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- Contribution to journal › Article
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Mark
Detection of a t(1;22)(q23;q 12) translocation leading to an EWSR1-PBX1 fusion gene in a myoepithelioma
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- Contribution to journal › Article