Maroulio Pertesi

Forskningsingenjör
Fler filtreringsmöjligheter
  1. 2019
  2. Essential genes shape cancer genomes through linear limitation of homozygous deletions

    Maroulio Pertesi, Ludvig Ekdahl, Palm, A., Ellinor Johnsson, Järvstråt, L., Anna Karin Wihlborg & Björn Nilsson, 2019, I : Communications Biology. 2, 1, 262.

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

  3. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

    Maroulio Pertesi, Björn Nilsson, McKay, J. D., Dumontet, C. & et al., 2019, I : Leukemia.

    Forskningsoutput: TidskriftsbidragLetter

  4. 2017
  5. Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation

    Apostolou, P., M. Pertesi, Aleporou-Marinou, V., Dimitrakakis, C., Papadimitriou, C., Razis, E., Christodoulou, C., Fountzilas, G., Yannoukakos, D., Konstantopoulou, I. & Fostira, F., 2017, I : Clinical Genetics. 91, 3, s. 482-487

    Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift