@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S,Stojanovski Natasa},
year={2024},
title={Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1384-1385},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Grk Milka B,Dusanovic-Pjevic Marija G,Djuranovic Ana S,Rasic Milica,Barzegar Parsa,El Hayani Badr,Perovic Dijana},
year={2024},
title={Chromosomal microarray analysis in children with syndromic short stature},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1115-1115},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Perovic Dijana,Maksimovic Nela S,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S},
year={2024},
title={Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1018-1018},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S,Stojanovski Natasa},
year={2024},
title={Enrichment of pathogenic copy number variants on 17q chromosome in patients with skeletal findings},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1384-1385},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maksimovic Nela S,Damnjanovic Tatjana M,Jekic Biljana B,Grk Milka B,Dusanovic-Pjevic Marija G,Djuranovic Ana S,Rasic Milica,Barzegar Parsa,El Hayani Badr,Perovic Dijana},
year={2024},
title={Chromosomal microarray analysis in children with syndromic short stature},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1115-1115},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Damnjanovic Tatjana M,Perovic Dijana,Maksimovic Nela S,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S},
year={2024},
title={Diagnostic yield of chromosomal microarray analysis in patients with congenital heart disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1018-1018},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Perovic Dijana,Maksimovic Nela S,Damnjanovic Tatjana M,Djuranovic Ana S,Sarajlija Adrijan,Mijovic Marija},
year={2023},
title={Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={267-268},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djuranovic Ana S,Cerovac Natasa M,Perovic Dijana,Stojanovski Natasa,Damnjanovic Tatjana M},
year={2023},
title={Study of IL6 and TNF genes polymorphisms as a risk factor for the development of early neurological disorders and subsequent consequences in neonates},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={171-171},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Perovic Dijana,Damnjanovic Tatjana M,Jekic Biljana B,Dusanovic-Pjevic Marija G,Grk Milka B,Djuranovic Ana S,Rasic Milica,Novakovic Ivana V,Maksimovic Nela S},
year={2022},
title={Chromosomal microarray in postnatal diagnosis of congenital anomalies and neurodevelopmental disorders in Serbian patients},
journal={JOURNAL OF CLINICAL LABORATORY ANALYSIS},
volume={36},
number={6},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Pesic Milica,Maksimovic Nela S,Aleksic Andjelka,Gulic Milica,Djuranovic Ana S,Grk Milka B,Dusanovic-Pjevic Marija G,Stankovic Iva D,Markovic Vladana V,Marjanovic Ana,Novakovic Ivana V,Dragasevic-Miskovic Natasa T,Kostic Vladimir S},
year={2020},
title={Polymorphisms in genes for proinflammatory cytokines IL-6, IL-1 ss, andTNF-alpha in relation with Parkinson's disease progression},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={888-888},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djuranovic Ana S,Cerovac Natasa M,Perovic Dijana,Grk Milka B,Pesic Milica,Damnjanovic Tatjana M},
year={2020},
title={Investigation of the MMP2 haplotype as a risk factor for the development of cerebral palsy},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={28},
number={SUPPL 1},
pages={351-351},
document_type={Meeting Abstract},
} 

