G. Bunjevački

发表

Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes.

I. Pastar, J. Milašin, I. Novaković, 2004, Cancer genetics and cytogenetics.

Glomerular involvement in myelodysplastic syndromes

M. Ognjanović, R. Bogdanović, N. Stajić, 2001, Pediatric Nephrology.

Biochemical phenotype and origin of the three most common beta-thalassemia mutations in Serbia

N. Tosic, L. Perisic, J. Urosevic, 2004 .

Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome.

J. Milašin, I. Novaković, B. Popović, 2006, Cancer genetics and cytogenetics.

Juvenile nephronophthisis associated with retinal pigmentary dystrophy, cerebellar ataxia, and skeletal abnormalities.

M. Popović-Rolović, G. Bunjevački, D. Negovanovic, 1976, Archives of disease in childhood.

Severe central nervous system thrombotic events in hemoglobin Sabine patient

M. Čolović, S. Pavlovic, T. Zoranovic, 2004, European journal of haematology.

Acute leukemia of childhood: A single institution's experience

A. Krstic, S. Djuricic, M. Kuzmanović, 2005 .

Haploidentical bone marrow transplantation in leukemia and genetic diseases.

A. Beorchia, C. Vidali, M. Rabusin, 2000, Haematologica.

Molecular Basis of Thalassemia Syndromes in Serbia and Montenegro

N. Tosic, S. Pavlovic, L. Perisic, 2005, Acta Haematologica.

BONE CHANGES, MINERAL HOMEOSTASIS IN CHILDHOOD ACUTE LYMPHOBLASTIC LEUKEMIA

B. Kamenov, G. Kostić, G. Bunjevački, 2004 .

Adhesion molecules in Wilms tumor (part II) : beta-catenin expression and significance

M. Radojević, M. Savin, S. Skodrić, 2003 .

Epstein–Barr virus associated hemophagocytic lymphohystiocytosis during maintenance treatment of acute lymphoblastic leukemia

S. Pašić, M. Kuzmanović, D. Mićić, 2006, Pediatric blood & cancer.