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You searched for: Author/Creator Kinalis, Savvas

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1. Application of whole‐exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia. (27th July 2017)

4. Genomic profiling of newly diagnosed glioblastoma patients and its potential for clinical utility – a prospective, translational study. Issue 11 (18th September 2020)

5. Molecular subtyping of breast cancer improves identification of both high and low risk patients. (2nd January 2018)