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IMAGINE
Institut za molekularnu genetiku i genetičko inženjerstvo
Grupa za molekularnu biomedicinu/ Group for Molecular Biomedicine 01
Browsing by Titles
IMAGINE
Institut za molekularnu genetiku i genetičko inženjerstvo
Grupa za molekularnu biomedicinu/ Group for Molecular Biomedicine 01
Browsing by Titles
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Titles
A Comparison of MGMT Testing by MSP and qMSP in Paired Snap-Frozen and Formalin-Fixed Paraffin-Embedded Gliomas
[1]
Association of Vitamin D, Zinc and Selenium Related Genetic Variants With COVID-19 Disease Severity
[1]
Brza progresija hronične limfocitne leukemije u Rihterov sindrom kod bolesnika sa kariotipom blizu triploidnog broja hromozom
[1]
Expression levels of BCL2, BAX and MDR1 as pharmacotranscriptomic and prognostic markers of prognosis in acute myeloid leukemia
[1]
Genetic determinants of response to neoadjuvant chemoradiotherapy in locally advanced rectal cancer identified by whole exome sequencing
[1]
Genomics as a basis for precision medicine
[1]
Hybridosomes from spruce needle homogenate
[2]
Micronutrients, genetics and COVID-19
[1]
Molecular profiling of rare thymoma using next-generation sequencing: meta-analysis
[1]
Pediatric acute myeloid leukemia: Insight into genetic landscape and novel targeted approaches
[1]
Pharmacogenomics and pharmacotranscriptomics of acute leukemia in children: a path to personalized medicine
[1]
Presence of leukemic clone-specific immunoglobulin heavy chain rearrangements in neonatal blood spots of children with B-cell precursor acute lymphoblastic leukemia
[1]
Prognostic significance of the long non-coding rna malat1 expression in chronic lymphocytic leukemia
[1]
Rapid progression to Richter’s syndrome in a patient with chronic lymphocytic leukemia and near-triploid karyotype
[1]
Rare case of myelodysplastic syndrome with near-tetraploidy and TP53 mutation
[1]
Signifi cance of molecular diagnosti cs in therapy of chronic lymphocytic leukemia
[1]
The pharmacogenomics of vincristine-induced peripheral neuropathy in pediatric acute lymphoblastic leukemia patients in Serbia
[1]
Мијелодиспластични синдром са приближном тетраплоидијом удруженом са мутацијом гена TP53 – редак случај
[1]
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