M. Guć-Šćekić

发表

Radiation-induced mitotic catastrophe in FANCD2 primary fibroblasts

G. Joksiċ, D. Vujić, S. Petrović, 2014, International journal of radiation biology.

Dysfunctional telomeres in primary cells from Fanconi anemia FANCD2 patients

G. Joksiċ, J. Surrallés, P. Slijepcevic, 2012, Genome Integrity.

Molecular diagnosis of childhood acute leukemia: Serbian experience

A. Krstic, D. Janić, D. Mićić, 2010, Pediatric blood & cancer.

G. Joksiċ, J. Kotur-Stevuljević, D. Vujić, 2011, Biological chemistry.

Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia

S. Ćirković, M. Guć-Šćekić, S. Ostojic, 2014, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.

G. Vlahović, S. Ćirković, D. Zamurović, 2011, The Tohoku journal of experimental medicine.

Comet assay and cytogenetic findings in differential diagnosis of Fanconi anemia

B. Vuković-Gačić, K. Sunjog, D. Vujić, 2019, Genetika.

Interstitial deletion of 11q.

M. Guć-Šćekić, M. Djurić, G. Pilić-Radivojević, 1989, Journal of medical genetics.

Chromosomal instability in patients with Fanconi anemia from Serbia.

D. Vujić, S. Ćirković, D. Mićić, 2014, Vojnosanitetski pregled.

A complex rearrangement involving cryptic deletion of ETV6 and CDKN1B genes in a case of childhood acute lymphoblastic leukemia.

C. Storlazzi, A. Krstic, L. Impera, 2009, Cancer genetics and cytogenetics.

Cytogenetic diepoxybutane sensitivity in Serbian children with Fanconi anemia

D. Vujić, S. Ćirković, D. Mićić, 2006 .

Prognostic value of clinical, genetic and cytogenetic findings in neuroblastoma patients from Serbia and Montenegro

S. Djuricic, D. Vujić, M. Guć-Šćekić, 2005 .

Fanconi anemia is characterized by delayed repair kinetics of DNA double-strand breaks.

G. Joksiċ, P. Slijepcevic, D. Vujić, 2010, The Tohoku journal of experimental medicine.

Enhanced frequency of sister chromatid exchanges induced by diepoxybutane is specific characteristic of Fanconi anemia cellular phenotype

G. Joksiċ, D. Vujić, S. Petrović, 2013 .

Monitoring of Pediatric Patients With Malignant Hematological Diseases After Allogeneic HSCT: Serbian Experience

A. Krstic, O. Stojković, D. Vujić, 2012, Journal of pediatric hematology/oncology.