A Pediatric Case of Glioblastoma Multiforme Associated With a Novel Germline p.His112CysfsTer9 Mutation in the MLH1 Gene Accompanied by a p.Arg283Cys Mutation in the TP53 Gene: A C...

por Stajkovska, Aleksandra, Mehandziska, Sanja, Rosalia, Rodney, Stavrevska, Margarita, Janevska, Marija, Markovska, Martina, Kungulovski, Ivan, Mitrev, Zan, Kungulovski, Goran
Publicado 2019

Workflow for the Implementation of Precision Genomics in Healthcare

por Mehandziska, Sanja, Stajkovska, Aleksandra, Stavrevska, Margarita, Jakovleva, Kristina, Janevska, Marija, Rosalia, Rodney, Kungulovski, Ivan, Mitrev, Zan, Kungulovski, Goran
Publicado 2020

Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans

por Stajkovska, Aleksandra, Mehandziska, Sanja, Stavrevska, Margarita, Jakovleva, Kristina, Nikchevska, Natasha, Mitrev, Zan, Kungulovski, Ivan, Zafiroski, Gjorgje, Tasic, Velibor, Kungulovski, Goran
Publicado 2018

Case Report: Omicron BA.2 Subvariant of SARS-CoV-2 Outcompetes BA.1 in Two Co-infection Cases

por Gjorgjievska, Marija, Mehandziska, Sanja, Stajkovska, Aleksandra, Pecioska-Dokuzovska, Slavica, Dimovska, Anica, Durmish, Idriz, Ismail, Sara, Pavlovska, Teodora, Stojchevska, Antonija, Amedi, Haris, Andonova, Jasna, Nikolovska, Marija, Velickovikj, Sara, Mitrev, Zan, Kungulovski, Ivan, Kungulovski, Goran
Publicado 2022