@ARTICLE{
author={Paripovic Aleksandra,Jankovic Aleksandar N,Ilic N,Ostojic Slavica B,Todorovic Sladjana,Radivojevic Danijela,Pejovic B,Naumovic Radomir T,Sarajlija Adrijan},
year={2025},
title={Townes-Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={28},
number={2},
pages={93-100},
document_type={Article},
} 

@ARTICLE{
author={Djurisic Marina,Sarajlija Adrijan,Radivojevic Danijela,Cirkovic Sanja,Djokic Dragoljub,Djuricic Slavisa M,Samardzija Gordana,Pasic Srdjan S},
year={2025},
title={Neuroblastoma Occurring in Nijmegen Breakage Syndrome},
journal={JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY},
volume={47},
number={1},
pages={e74-e76},
document_type={Article},
} 

@ARTICLE{
author={Ilic Nikola A,Maric Nina,...,Kravljanac Ruzica M,Cirkovic Jana,Krstic Jovana,Radivojevic Danijela,Cirkovic Sanja S,Ostojic Slavica B,Krasic Stasa D,Paripovic Aleksandra,Vukomanovic Vladislav A,...,Maric Gorica D,Sarajlija Adrijan},
year={2024},
title={Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?},
journal={GENES},
volume={15},
number={6},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Cupurdija Maja,Miskovic Marijana,Cirkovic Sanja S,Radivojevic Danijela,Ilic Nina,Lalic Tanja,Dobric Bojana,Djurisic Marina},
year={2024},
title={Genetic diagnosis of dup15q syndrome in a group of patients from Serbia},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={231-232},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Dobric Bojana,Radivojevic Danijela,Jecmenica Jovana R,Fanis Pavlos,Neocleous Vassos,Phylactou Leonidas A,Djurisic Marina},
year={2022},
title={Prevalence of Variants in DFNB1 Locus in Serbian Patients with Autosomal Recessive Non-Syndromic Hearing Loss},
journal={GENETIKA-BELGRADE},
volume={54},
number={1},
pages={447-456},
document_type={Article},
} 

@ARTICLE{
author={Kosac Ana P,Pesovic Jovan,Radenkovic Lana,Brkusanin Milos,Radovanovic Nemanja,Djurisic Marina,Radivojevic Danijela,Mladenovic Jelena M,Ostojic Slavica B,Kovacevic Gordana S,Kravljanac Ruzica M,Savic-Pavicevic Dusanka Lj,Milic-Rasic Vedrana M},
year={2022},
title={LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients},
journal={GENES},
volume={13},
number={8},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Dobric Bojana,Radivojevic Danijela,Jecmenica Jovana R,Neocleous Vassos,Fanis Pavlos,Phylactou Leonidas A,Djurisic Marina},
year={2021},
title={Audiological features in Serbian patients with hearing impairment identified with c.35delG in the GJB2 gene},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={149},
number={11-12},
pages={685-690},
document_type={Article},
} 

@ARTICLE{
author={Dobric Bojana,Radivojevic Danijela,Lalic Tanja,Miskovic Marijana,Cirkovic Sanja S,Djordjevic Maja S,Djurisic Marina},
year={2019},
title={Incidence of Genetic Causes of Idiopathic Male Infertility in Serbia - Ten Years' Experience of Single Centre},
journal={GENETIKA-BELGRADE},
volume={51},
number={3},
pages={1009-1019},
document_type={Article},
} 

@ARTICLE{
author={Dobric Bojana,Jecmenica Jovana R,Radivojevic Danijela,Djurisic Marina},
year={2018},
title={First results of genetic testing of non syndromic hearing impairment in patients from Serbia- case report of family with multiple affected members},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={26},
number={},
pages={845-845},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Aguilera Cinthia,Vinas-Jornet Marina,Baena Neus,Gabau Elisabeth,Fernandez Concepcion,Capdevila Nuria,Cirkovic Sanja S,Sarajlija Adrijan,Miskovic Marijana,Radivojevic Danijela,Ruiz Anna,Guitart Miriam},
year={2017},
title={Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature},
journal={BMC MEDICAL GENETICS},
volume={18},
number={},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Miskovic Marijana,Lalic Tanja,Radivojevic Danijela,Cirkovic Sanja S,Ostojic Slavica B,Guc-Scekic Marija P},
year={2014},
title={Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia},
journal={INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS},
volume={124},
number={1},
pages={55-58},
document_type={Article},
} 

@ARTICLE{
author={Radivojevic Danijela,Sovtic Aleksandar D,Minic Predrag B,Grkovic Sanja,Guc-Scekic Marija P,Lalic Tanja,Miskovic Marijana},
year={2013},
title={Newborn screening for cystic fibrosis in Serbia: A pilot study},
journal={PEDIATRICS INTERNATIONAL},
volume={55},
number={2},
pages={181-184},
document_type={Article},
} 

@ARTICLE{
author={Guc-Scekic Marija P,Milenkovic Tatjana,Zdravkovic Dragan S,Topic Vesna,Liehr Thomas,Joksic Gordana,Radivojevic Danijela,Lakic Nina},
year={2011},
title={Classic and molecular cytogenetic findings in a 10-year-old boy with ring Y chromosome mosaicism: a case report},
journal={CHROMOSOME RESEARCH},
volume={19},
number={},
pages={S38-S39},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Milenkovic Tatjana,Guc-Scekic Marija P,Zdravkovic Dragan S,Topic Vesna,Liehr Thomas,Joksic Gordana,Radivojevic Danijela,Lakic Nina},
year={2011},
title={Molecular Analysis of Ring Y Chromosome in a 10-Year-Old Boy with Mixed Gonadal Dysgenesis and Growth Hormone Deficiency},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={14},
number={2},
pages={71-76},
document_type={Article},
} 

@ARTICLE{
author={Miskovic Marijana,Lalic Tanja,Radivojevic Danijela,Cirkovic Sanja S,Vlahovic Gordana,Zamurovic Dragan R,Guc-Scekic Marija P},
year={2011},
title={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},
journal={TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE},
volume={225},
number={3},
pages={153-159},
document_type={Article},
} 

@ARTICLE{
author={Radivojevic Danijela,Lalic Tanja,Djurisic Marina,Guc-Scekic Marija P,Minic Predrag B,Sovtic Aleksandar D},
year={2008},
title={Analysis of extra- and intragenic marker haplotypes as part of molecular diagnosis of cystic fibrosis in patients from Serbia},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={60},
number={1},
pages={5-10},
document_type={Article},
} 

@ARTICLE{
author={Lalic Tanja,Vossen RH,Coffa J,Schouten JP,Guc-Scekic Marija P,Radivojevic Danijela,Djurisic Marina,Breuning MH,White SJ,den Dunnen JT},
year={2005},
title={Deletion and duplication screening in the DMD gene using MLPA},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={13},
number={11},
pages={1231-1234},
document_type={Article},
} 

@ARTICLE{
author={Radivojevic Danijela,Djurisic Marina,Lalic Tanja,Guc-Scekic Marija P,Savic Jovan,Minic Predrag B,Antoniadi T,Tzetis M,Kanavakis E},
year={2004},
title={Spectrum of cystic fibrosis mutations in Serbia and Montenegro and strategy for prenatal diagnosis},
journal={GENETIC TESTING},
volume={8},
number={3},
pages={276-280},
document_type={Article},
} 

@ARTICLE{
author={Radivojevic Danijela,Djurisic Marina,Minic Predrag B,Guc-Scekic Marija P,Lalic Tanja},
year={2002},
title={Genotype-phenotype correlations in a group of Yugoslavian adult cystic fibrosis patients},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={10},
number={},
pages={138-139},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djurisic Marina,Guc-Scekic Marija P,Radivojevic Danijela,Lalic Tanja,Djuricic Slavisa M,Djokic Dragan},
year={2002},
title={Cytogenetic and molecular genetic characterization of patients with neuroblastoma in Yugoslavia},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={10},
number={},
pages={105-105},
document_type={Meeting Abstract},
}