Претрага

Резултати

Rare missense TUBGCP5 gene variant in a patient with primary microcephaly (✓) [2019]

Maver, Aleš; Čuturilo, Goran ; Kovanda, Anja; Miletić, Aleksandra; Peterlin, Borut

Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21 [2005]

Riegel, M; Hargreaves, P; Baumer, A; Guc-Scekic, Marija P; Ignjatovic, M; Schinzel, A

Pan-european landscape of research into neurodevelopmental copy number variants: A survey by the MINDDS consortium [2020]

Chawner, Samuel JRA; Mihaljevic, Marina M; Morrison, Sinead; Eser, Hale Yapici; Maillard, Anne M; Nowakowska, Beata; Van, den Bree Marianne BM; Swillen, Ann

Cytogenetic biomarkers in detection of genotoxic effects of gestagens in peripheral blood lymphocytes in vitro and in vivo (✓) [2016]

Grujičić, Darko ; Radović M. ; Arsenijevic, Slobodan ; Milošević-Đorđević, Olivera

Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib (✓) [2020]

Sarajlija, Adrijan ; Đorđević, Maja ; Kecman, Božica; Skakić, Anita ; Pavlović, Sonja ; Pašić, Srđan ; Stojiljković, Maja

A case of splenomegaly in CBL syndrome [2017]

Coe, Rachel R; McKinnon, Margaret L; Tarailo-Graovac, Maja; Ross, Colin J; Wasserman, Wyeth W; Friedman, Jan M; Rogers, Paul C; van, Karnebeek Clara DM