TY  - CONF
AU  - Perić, Jelena
AU  - Karan-Đurašević, Teodora
AU  - Kostić, Tatjana 
AU  - Marjanović, Irena
AU  - Lazić, J.
AU  - Virijević, M.
AU  - Krstovski, N.
AU  - Dokmanović, Lidija
AU  - Tomin, D.
AU  - Vidović, A.
AU  - Suvajdžić-Vuković, Nada
AU  - Janić, D.
AU  - Pavlović, Sonja
AU  - Tošić, Nataša
PY  - 2017
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/1071
PB  - Ferrata Storti Foundation, Pavia
C3  - Haematologica-The Hematology Journal
T1  - Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients
EP  - 653
SP  - 653
VL  - 102
UR  - https://hdl.handle.net/21.15107/rcub_imagine_1071
ER  - 

@conference{
author = "Perić, Jelena and Karan-Đurašević, Teodora and Kostić, Tatjana  and Marjanović, Irena and Lazić, J. and Virijević, M. and Krstovski, N. and Dokmanović, Lidija and Tomin, D. and Vidović, A. and Suvajdžić-Vuković, Nada and Janić, D. and Pavlović, Sonja and Tošić, Nataša",
year = "2017",
publisher = "Ferrata Storti Foundation, Pavia",
journal = "Haematologica-The Hematology Journal",
title = "Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients",
pages = "653-653",
volume = "102",
url = "https://hdl.handle.net/21.15107/rcub_imagine_1071"
}

Perić, J., Karan-Đurašević, T., Kostić, T., Marjanović, I., Lazić, J., Virijević, M., Krstovski, N., Dokmanović, L., Tomin, D., Vidović, A., Suvajdžić-Vuković, N., Janić, D., Pavlović, S.,& Tošić, N.. (2017). Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients. in Haematologica-The Hematology Journal
Ferrata Storti Foundation, Pavia., 102, 653-653.
https://hdl.handle.net/21.15107/rcub_imagine_1071

Perić J, Karan-Đurašević T, Kostić T, Marjanović I, Lazić J, Virijević M, Krstovski N, Dokmanović L, Tomin D, Vidović A, Suvajdžić-Vuković N, Janić D, Pavlović S, Tošić N. Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients. in Haematologica-The Hematology Journal. 2017;102:653-653.
https://hdl.handle.net/21.15107/rcub_imagine_1071 .

Perić, Jelena, Karan-Đurašević, Teodora, Kostić, Tatjana , Marjanović, Irena, Lazić, J., Virijević, M., Krstovski, N., Dokmanović, Lidija, Tomin, D., Vidović, A., Suvajdžić-Vuković, Nada, Janić, D., Pavlović, Sonja, Tošić, Nataša, "Targeted mutational profiling of childhood and adult acute lymphoblastic leukemia patients" in Haematologica-The Hematology Journal, 102 (2017):653-653,
https://hdl.handle.net/21.15107/rcub_imagine_1071 .

TY  - CONF
AU  - Glumac, Irena
AU  - Kostić, Jelena
AU  - Stanić, B.
AU  - Pejanović, N.
AU  - Lucić, B.
AU  - Karan-Đurašević, Teodora
AU  - Janić, D.
AU  - Dokmanović, Lidija
AU  - Janković, S.
AU  - Suvajdžić-Vuković, Nada
AU  - Tomin, D.
AU  - Popović, M.
AU  - Bogicević, I.
AU  - Pavlović, Sonja
AU  - Tošić, Nataša
PY  - 2015
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/824
PB  - Ferrata Storti Foundation, Pavia
C3  - Haematologica-The Hematology Journal
T1  - Targeted next generation sequencing (ngs) in parallel analyses of childhood (caml) and adult acute myeloid leukemia (AAML) patients
EP  - 360
SP  - 360
VL  - 100
UR  - https://hdl.handle.net/21.15107/rcub_imagine_824
ER  - 

@conference{
author = "Glumac, Irena and Kostić, Jelena and Stanić, B. and Pejanović, N. and Lucić, B. and Karan-Đurašević, Teodora and Janić, D. and Dokmanović, Lidija and Janković, S. and Suvajdžić-Vuković, Nada and Tomin, D. and Popović, M. and Bogicević, I. and Pavlović, Sonja and Tošić, Nataša",
year = "2015",
publisher = "Ferrata Storti Foundation, Pavia",
journal = "Haematologica-The Hematology Journal",
title = "Targeted next generation sequencing (ngs) in parallel analyses of childhood (caml) and adult acute myeloid leukemia (AAML) patients",
pages = "360-360",
volume = "100",
url = "https://hdl.handle.net/21.15107/rcub_imagine_824"
}

Glumac, I., Kostić, J., Stanić, B., Pejanović, N., Lucić, B., Karan-Đurašević, T., Janić, D., Dokmanović, L., Janković, S., Suvajdžić-Vuković, N., Tomin, D., Popović, M., Bogicević, I., Pavlović, S.,& Tošić, N.. (2015). Targeted next generation sequencing (ngs) in parallel analyses of childhood (caml) and adult acute myeloid leukemia (AAML) patients. in Haematologica-The Hematology Journal
Ferrata Storti Foundation, Pavia., 100, 360-360.
https://hdl.handle.net/21.15107/rcub_imagine_824

Glumac I, Kostić J, Stanić B, Pejanović N, Lucić B, Karan-Đurašević T, Janić D, Dokmanović L, Janković S, Suvajdžić-Vuković N, Tomin D, Popović M, Bogicević I, Pavlović S, Tošić N. Targeted next generation sequencing (ngs) in parallel analyses of childhood (caml) and adult acute myeloid leukemia (AAML) patients. in Haematologica-The Hematology Journal. 2015;100:360-360.
https://hdl.handle.net/21.15107/rcub_imagine_824 .

Glumac, Irena, Kostić, Jelena, Stanić, B., Pejanović, N., Lucić, B., Karan-Đurašević, Teodora, Janić, D., Dokmanović, Lidija, Janković, S., Suvajdžić-Vuković, Nada, Tomin, D., Popović, M., Bogicević, I., Pavlović, Sonja, Tošić, Nataša, "Targeted next generation sequencing (ngs) in parallel analyses of childhood (caml) and adult acute myeloid leukemia (AAML) patients" in Haematologica-The Hematology Journal, 100 (2015):360-360,
https://hdl.handle.net/21.15107/rcub_imagine_824 .

TY  - CONF
AU  - Lazić, J.
AU  - Dokmanović, Lidija
AU  - Krstovski, N.
AU  - Pavlović, Sonja
AU  - Zukić, Branka
AU  - Kotur, Nikola
AU  - Milosević, G.
AU  - Janić, D.
PY  - 2013
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/693
PB  - Elsevier Sci Ltd, Oxford
C3  - European Journal of Cancer
T1  - Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia
EP  - S358
SP  - S358
VL  - 49
UR  - https://hdl.handle.net/21.15107/rcub_imagine_693
ER  - 

@conference{
author = "Lazić, J. and Dokmanović, Lidija and Krstovski, N. and Pavlović, Sonja and Zukić, Branka and Kotur, Nikola and Milosević, G. and Janić, D.",
year = "2013",
publisher = "Elsevier Sci Ltd, Oxford",
journal = "European Journal of Cancer",
title = "Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia",
pages = "S358-S358",
volume = "49",
url = "https://hdl.handle.net/21.15107/rcub_imagine_693"
}

Lazić, J., Dokmanović, L., Krstovski, N., Pavlović, S., Zukić, B., Kotur, N., Milosević, G.,& Janić, D.. (2013). Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia. in European Journal of Cancer
Elsevier Sci Ltd, Oxford., 49, S358-S358.
https://hdl.handle.net/21.15107/rcub_imagine_693

Lazić J, Dokmanović L, Krstovski N, Pavlović S, Zukić B, Kotur N, Milosević G, Janić D. Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia. in European Journal of Cancer. 2013;49:S358-S358.
https://hdl.handle.net/21.15107/rcub_imagine_693 .

Lazić, J., Dokmanović, Lidija, Krstovski, N., Pavlović, Sonja, Zukić, Branka, Kotur, Nikola, Milosević, G., Janić, D., "Association between MTHFR, SLC19A1 and DHFR genetic polymorphisms and clinical and biochemical parameters of methotrexate induced toxicity in children with acute lymphoblastic leukaemia" in European Journal of Cancer, 49 (2013):S358-S358,
https://hdl.handle.net/21.15107/rcub_imagine_693 .

TY  - JOUR
AU  - Lazić, J.
AU  - Tošić, Nataša
AU  - Dokmanović, Lidija
AU  - Krstovski, N.
AU  - Rodić, P.
AU  - Pavlović, Sonja
AU  - Janić, D.
PY  - 2010
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/423
AB  - Contemporary protocols ensure high-remission rate and long-term free survival in children with acute lymphoblastic leukemia (ALL), but small percentage of patients is still incurable. Molecular genetic methods helped to establish submicroscopic classification as well as minimal residual disease follow-up, considered to be responsible for relapse. Our study enrolled 70 pediatric patients with de novo ALL, analyzed using reverse transcriptase-polymerase chain reaction for the presence of four major risk-stratifying translocations (BCR/ABL, MLL/AF4, TEL/AML1, and E2A/PBX1). Bone marrow samples were collected at diagnosis, at the end of induction phase, and after intensive chemotherapy with the aim to establish the correlation between chromosomal aberration, clinical features, and treatment response. Presenting the results of this study, we offer another evidence of variable incidence and clinical characteristics of ALL subtypes.
PB  - Humana Press Inc, Totowa
T2  - Medical Oncology
T1  - Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia
EP  - 453
IS  - 2
SP  - 449
VL  - 27
DO  - 10.1007/s12032-009-9232-x
ER  - 

@article{
author = "Lazić, J. and Tošić, Nataša and Dokmanović, Lidija and Krstovski, N. and Rodić, P. and Pavlović, Sonja and Janić, D.",
year = "2010",
abstract = "Contemporary protocols ensure high-remission rate and long-term free survival in children with acute lymphoblastic leukemia (ALL), but small percentage of patients is still incurable. Molecular genetic methods helped to establish submicroscopic classification as well as minimal residual disease follow-up, considered to be responsible for relapse. Our study enrolled 70 pediatric patients with de novo ALL, analyzed using reverse transcriptase-polymerase chain reaction for the presence of four major risk-stratifying translocations (BCR/ABL, MLL/AF4, TEL/AML1, and E2A/PBX1). Bone marrow samples were collected at diagnosis, at the end of induction phase, and after intensive chemotherapy with the aim to establish the correlation between chromosomal aberration, clinical features, and treatment response. Presenting the results of this study, we offer another evidence of variable incidence and clinical characteristics of ALL subtypes.",
publisher = "Humana Press Inc, Totowa",
journal = "Medical Oncology",
title = "Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia",
pages = "453-449",
number = "2",
volume = "27",
doi = "10.1007/s12032-009-9232-x"
}

Lazić, J., Tošić, N., Dokmanović, L., Krstovski, N., Rodić, P., Pavlović, S.,& Janić, D.. (2010). Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia. in Medical Oncology
Humana Press Inc, Totowa., 27(2), 449-453.
https://doi.org/10.1007/s12032-009-9232-x

Lazić J, Tošić N, Dokmanović L, Krstovski N, Rodić P, Pavlović S, Janić D. Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia. in Medical Oncology. 2010;27(2):449-453.
doi:10.1007/s12032-009-9232-x .

Lazić, J., Tošić, Nataša, Dokmanović, Lidija, Krstovski, N., Rodić, P., Pavlović, Sonja, Janić, D., "Clinical features of the most common fusion genes in childhood acute lymphoblastic leukemia" in Medical Oncology, 27, no. 2 (2010):449-453,
https://doi.org/10.1007/s12032-009-9232-x . .

TY  - CONF
AU  - Radmilović, Milena
AU  - Zukić, Branka
AU  - Stojiljković, Maja
AU  - Tošić, Nataša
AU  - Pourfarzad, F.
AU  - Dokmanović, Lidija
AU  - Janić, D.
AU  - Čolović, Nataša
AU  - Philipsen, S.
AU  - Patrinos, G.
AU  - Pavlović, Sonja
PY  - 2010
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/418
PB  - Ferrata Storti Foundation, Pavia
C3  - Haematologica-The Hematology Journal
T1  - VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy
EP  - 683
SP  - 682
VL  - 95
UR  - https://hdl.handle.net/21.15107/rcub_imagine_418
ER  - 

@conference{
author = "Radmilović, Milena and Zukić, Branka and Stojiljković, Maja and Tošić, Nataša and Pourfarzad, F. and Dokmanović, Lidija and Janić, D. and Čolović, Nataša and Philipsen, S. and Patrinos, G. and Pavlović, Sonja",
year = "2010",
publisher = "Ferrata Storti Foundation, Pavia",
journal = "Haematologica-The Hematology Journal",
title = "VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy",
pages = "683-682",
volume = "95",
url = "https://hdl.handle.net/21.15107/rcub_imagine_418"
}

Radmilović, M., Zukić, B., Stojiljković, M., Tošić, N., Pourfarzad, F., Dokmanović, L., Janić, D., Čolović, N., Philipsen, S., Patrinos, G.,& Pavlović, S.. (2010). VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy. in Haematologica-The Hematology Journal
Ferrata Storti Foundation, Pavia., 95, 682-683.
https://hdl.handle.net/21.15107/rcub_imagine_418

Radmilović M, Zukić B, Stojiljković M, Tošić N, Pourfarzad F, Dokmanović L, Janić D, Čolović N, Philipsen S, Patrinos G, Pavlović S. VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy. in Haematologica-The Hematology Journal. 2010;95:682-683.
https://hdl.handle.net/21.15107/rcub_imagine_418 .

Radmilović, Milena, Zukić, Branka, Stojiljković, Maja, Tošić, Nataša, Pourfarzad, F., Dokmanović, Lidija, Janić, D., Čolović, Nataša, Philipsen, S., Patrinos, G., Pavlović, Sonja, "VNTR polymorphisms in tpmt gene promoter: potential tool for thiopurine-guided therapy" in Haematologica-The Hematology Journal, 95 (2010):682-683,
https://hdl.handle.net/21.15107/rcub_imagine_418 .

TY  - CONF
AU  - Janić, D.
AU  - Rodić, P.
AU  - Kostić, Tatjana 
AU  - Đorđević, N.
AU  - Suvajdžić, Nada
PY  - 2008
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/318
PB  - Elsevier, Bridgewater
C3  - Clinical Therapeutics
T1  - Monoclonal gammopathy and lymphocyte clonality in patients with gaucher disease
EP  - S99
SP  - S98
VL  - 30
UR  - https://hdl.handle.net/21.15107/rcub_imagine_318
ER  - 

@conference{
author = "Janić, D. and Rodić, P. and Kostić, Tatjana  and Đorđević, N. and Suvajdžić, Nada",
year = "2008",
publisher = "Elsevier, Bridgewater",
journal = "Clinical Therapeutics",
title = "Monoclonal gammopathy and lymphocyte clonality in patients with gaucher disease",
pages = "S99-S98",
volume = "30",
url = "https://hdl.handle.net/21.15107/rcub_imagine_318"
}

Janić, D., Rodić, P., Kostić, T., Đorđević, N.,& Suvajdžić, N.. (2008). Monoclonal gammopathy and lymphocyte clonality in patients with gaucher disease. in Clinical Therapeutics
Elsevier, Bridgewater., 30, S98-S99.
https://hdl.handle.net/21.15107/rcub_imagine_318

Janić D, Rodić P, Kostić T, Đorđević N, Suvajdžić N. Monoclonal gammopathy and lymphocyte clonality in patients with gaucher disease. in Clinical Therapeutics. 2008;30:S98-S99.
https://hdl.handle.net/21.15107/rcub_imagine_318 .

Janić, D., Rodić, P., Kostić, Tatjana , Đorđević, N., Suvajdžić, Nada, "Monoclonal gammopathy and lymphocyte clonality in patients with gaucher disease" in Clinical Therapeutics, 30 (2008):S98-S99,
https://hdl.handle.net/21.15107/rcub_imagine_318 .

TY  - JOUR
AU  - Pavlović, Sonja
AU  - Urosević, J
AU  - Poznanić, J
AU  - Perisić, LJ
AU  - Petručev, Branka
AU  - Tošić, Nataša
AU  - Krivokapić-Dokmanović, L
AU  - Janić, D
AU  - Cvorkov-Drazić, M
AU  - Bunjevacki, G
PY  - 2005
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/226
AB  - This study reports the molecular characterization of thalassemia syndromes in Serbian and Montenegrin populations. We identified eight beta-thalassemia mutations [codon 39 (C - gt  T), IVS-I-110 (G - gt  A), IVS-II-745 (C - gt  G), codon 44 (-C), -87 (C - gt  G), IVS-II-1 (G - gt  A), IVS-I-6 (T - gt  C), IVS I-1 (G - gt  A)] in 70 members of 29 families using polymerase chain reaction, reverse dot blot, amplification refractory mutation system and direct sequencing analysis. Hemoglobin (Hb) Lepore was found to be the most common cause of the thalassemia phenotype. Hb Sabine and alpha-thalassemia were detected as well. We also studied beta-globin gene cluster haplotypes and their association with the most common mutations. A novel haplotype associated with the Hb Lepore gene was identified. The results presented herein allowed the implementation of a prenatal diagnosis program in Serbia and Montenegro.
PB  - Karger, Basel
T2  - Acta Haematologica
T1  - Molecular basis of Thalassemia syndromes in Serbia and Montenegro
EP  - 180
IS  - 3
SP  - 175
VL  - 113
DO  - 10.1159/000084447
ER  - 

@article{
author = "Pavlović, Sonja and Urosević, J and Poznanić, J and Perisić, LJ and Petručev, Branka and Tošić, Nataša and Krivokapić-Dokmanović, L and Janić, D and Cvorkov-Drazić, M and Bunjevacki, G",
year = "2005",
abstract = "This study reports the molecular characterization of thalassemia syndromes in Serbian and Montenegrin populations. We identified eight beta-thalassemia mutations [codon 39 (C - gt  T), IVS-I-110 (G - gt  A), IVS-II-745 (C - gt  G), codon 44 (-C), -87 (C - gt  G), IVS-II-1 (G - gt  A), IVS-I-6 (T - gt  C), IVS I-1 (G - gt  A)] in 70 members of 29 families using polymerase chain reaction, reverse dot blot, amplification refractory mutation system and direct sequencing analysis. Hemoglobin (Hb) Lepore was found to be the most common cause of the thalassemia phenotype. Hb Sabine and alpha-thalassemia were detected as well. We also studied beta-globin gene cluster haplotypes and their association with the most common mutations. A novel haplotype associated with the Hb Lepore gene was identified. The results presented herein allowed the implementation of a prenatal diagnosis program in Serbia and Montenegro.",
publisher = "Karger, Basel",
journal = "Acta Haematologica",
title = "Molecular basis of Thalassemia syndromes in Serbia and Montenegro",
pages = "180-175",
number = "3",
volume = "113",
doi = "10.1159/000084447"
}

Pavlović, S., Urosević, J., Poznanić, J., Perisić, L., Petručev, B., Tošić, N., Krivokapić-Dokmanović, L., Janić, D., Cvorkov-Drazić, M.,& Bunjevacki, G.. (2005). Molecular basis of Thalassemia syndromes in Serbia and Montenegro. in Acta Haematologica
Karger, Basel., 113(3), 175-180.
https://doi.org/10.1159/000084447

Pavlović S, Urosević J, Poznanić J, Perisić L, Petručev B, Tošić N, Krivokapić-Dokmanović L, Janić D, Cvorkov-Drazić M, Bunjevacki G. Molecular basis of Thalassemia syndromes in Serbia and Montenegro. in Acta Haematologica. 2005;113(3):175-180.
doi:10.1159/000084447 .

Pavlović, Sonja, Urosević, J, Poznanić, J, Perisić, LJ, Petručev, Branka, Tošić, Nataša, Krivokapić-Dokmanović, L, Janić, D, Cvorkov-Drazić, M, Bunjevacki, G, "Molecular basis of Thalassemia syndromes in Serbia and Montenegro" in Acta Haematologica, 113, no. 3 (2005):175-180,
https://doi.org/10.1159/000084447 . .

TY  - JOUR
AU  - Urosević, J.
AU  - Đureinović, T.
AU  - Poznanić, J.
AU  - Cvorkov-Drazić, M.
AU  - Bunjevacki, G.
AU  - Janić, D.
AU  - Krivokapić-Dokmanović, L.
AU  - Popović, Z.
AU  - Pavlović, Sonja
PY  - 2001
UR  - https://imagine.imgge.bg.ac.rs/handle/123456789/152
AB  - Screening analysis of Yugoslav patients with suspected thalassemia syndromes in last 4 years revealed six patients who were Hb Lepore carriers. Three were compound heterozygotes for Hb Lepore and β-thalassemia, and they were affected with a thalassemia major syndrome. Family studies revealed 12 heterozygous relatives. All heterozygous carriers of Hb Lepore had a clinical phenotype of thalassemia trait. The detection of Hb Lepore was carried out by electrophoresis on cellulose acetate and confirmed by gap-polymerase chain reaction analysis of patients' DNA. Sequence analysis of all the Hb Lepore genes showed the same DNA sequence, indicating that the mutation was of the Hb Lepore-Boston-Washington type. Moreover, a single base substitution within the second intervening sequence [IVS-II-74 (G→T)] was detected in all analyzed hybrid genes. The molecular characteristics of this homogeneity represent additional data for the probable Balkan origin of this mutation.
PB  - Macedonian Academy Of Sciences And Arts
T2  - Balkan Journal of Medical Genetics
T1  - Homogeneity of the Hb Lepore gene in FR Yugoslavia
EP  - 32
IS  - 1-2
SP  - 29
VL  - 4
UR  - https://hdl.handle.net/21.15107/rcub_imagine_152
ER  - 

@article{
author = "Urosević, J. and Đureinović, T. and Poznanić, J. and Cvorkov-Drazić, M. and Bunjevacki, G. and Janić, D. and Krivokapić-Dokmanović, L. and Popović, Z. and Pavlović, Sonja",
year = "2001",
abstract = "Screening analysis of Yugoslav patients with suspected thalassemia syndromes in last 4 years revealed six patients who were Hb Lepore carriers. Three were compound heterozygotes for Hb Lepore and β-thalassemia, and they were affected with a thalassemia major syndrome. Family studies revealed 12 heterozygous relatives. All heterozygous carriers of Hb Lepore had a clinical phenotype of thalassemia trait. The detection of Hb Lepore was carried out by electrophoresis on cellulose acetate and confirmed by gap-polymerase chain reaction analysis of patients' DNA. Sequence analysis of all the Hb Lepore genes showed the same DNA sequence, indicating that the mutation was of the Hb Lepore-Boston-Washington type. Moreover, a single base substitution within the second intervening sequence [IVS-II-74 (G→T)] was detected in all analyzed hybrid genes. The molecular characteristics of this homogeneity represent additional data for the probable Balkan origin of this mutation.",
publisher = "Macedonian Academy Of Sciences And Arts",
journal = "Balkan Journal of Medical Genetics",
title = "Homogeneity of the Hb Lepore gene in FR Yugoslavia",
pages = "32-29",
number = "1-2",
volume = "4",
url = "https://hdl.handle.net/21.15107/rcub_imagine_152"
}

Urosević, J., Đureinović, T., Poznanić, J., Cvorkov-Drazić, M., Bunjevacki, G., Janić, D., Krivokapić-Dokmanović, L., Popović, Z.,& Pavlović, S.. (2001). Homogeneity of the Hb Lepore gene in FR Yugoslavia. in Balkan Journal of Medical Genetics
Macedonian Academy Of Sciences And Arts., 4(1-2), 29-32.
https://hdl.handle.net/21.15107/rcub_imagine_152

Urosević J, Đureinović T, Poznanić J, Cvorkov-Drazić M, Bunjevacki G, Janić D, Krivokapić-Dokmanović L, Popović Z, Pavlović S. Homogeneity of the Hb Lepore gene in FR Yugoslavia. in Balkan Journal of Medical Genetics. 2001;4(1-2):29-32.
https://hdl.handle.net/21.15107/rcub_imagine_152 .

Urosević, J., Đureinović, T., Poznanić, J., Cvorkov-Drazić, M., Bunjevacki, G., Janić, D., Krivokapić-Dokmanović, L., Popović, Z., Pavlović, Sonja, "Homogeneity of the Hb Lepore gene in FR Yugoslavia" in Balkan Journal of Medical Genetics, 4, no. 1-2 (2001):29-32,
https://hdl.handle.net/21.15107/rcub_imagine_152 .