Pretraga

Rezultati

Novel BRCA1/2 mutations in Serbian breast and breast-ovarian cancer patients with hereditary predisposition [2010]

Dobričić, Jelena ; Branković-Magić, Mirjana ; Filipović, Slađana ; Radulović, Siniša

An intronic variant in the TP53 gene in Serbian women with cervical or ovarian cancer [2010]

Janković, Radmila ; Mališić, Emina ; Radulović, Siniša

Multiple karyotypic aberrations in a polymorphous variant of Waldenstrom macroglobulinemia [1999]

Janković, Gradimir M. ; Čolović, Milica D. ; Wiernik, Peter H.; Antić, Nikola B.; Rajić, Zoran A.; Vidović, Ana D. ; Pantić, M.; Čolović, Nataša R.

Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome [2006]

Jekić, B. ; Novaković, I. ; Luković, L; Kuzmanović, M ; Popović, Branka ; Milašin, Jelena ; Bunjevacki, G; Damnjanović, Tatjana ; Cvjetičanin, S ; Bunjevački, Vera

Pattern of trisomy 1q in hematological malignancies: a single institution experience [2008]

Đorđević, Vesna; Denčić-Fekete, Marija; Jovanović, Jelica; Drakulić, Danijela ; Stevanović, Milena ; Janković, Gradimir; Gotić, Mirjana

Late-appearing pseudocentric fission event during chronic myeloid leukemia progression [2007]

Storlazzi, Clelia Tiziana; Albano, Francesco; Denčić-Fekete, Marija; Đorđević, Vesna ; Rocchi, Mariano

Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review [2009]

Tošić, Nataša ; Stojiljković, Maja ; Čolović, Nataša; Colović, Milica; Pavlović, Sonja

Novel BRCA1/2 mutations in Serbian breast and breast-ovarian cancer patients with hereditary predisposition [2010]

An intronic variant in the TP53 gene in Serbian women with cervical or ovarian cancer [2010]

Multiple karyotypic aberrations in a polymorphous variant of Waldenstrom macroglobulinemia [1999]

Lack of TP53 and FMS gene mutations in children with myelodysplastic syndrome [2006]

Pattern of trisomy 1q in hematological malignancies: a single institution experience [2008]

Late-appearing pseudocentric fission event during chronic myeloid leukemia progression [2007]

Acute myeloid leukemia with NUP98-HOXC13 fusion and FLT3 internal tandem duplication mutation: case report and literature review [2009]

Refractory anemia with ring sideroblasts associated with i(17q) and mutation of the TP53 gene [2002]

Sister chromatid exchanges in patients with carcinoma in situ of cervix uteri [1992]

Low frequency of NRAS and KRAS2 gene mutations in childhood myelodysplastic syndromes [2004]

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