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Metoidioplasty

Urologic clinics of North America, 2019-11, Vol.46 (4), p.555-566

2019

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Isolated Male Epispadias Repair: Long-Term Outcomes

Life (Basel, Switzerland), 2024-04, Vol.14 (4), p.446

2024

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Small supernumerary marker chromosomes in prenatal diagnosis-molecular characterization and clinical outcomes

Frontiers in genetics, 2024-01, Vol.14, p.1326985

2024

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Autism spectrum disorder and Coffin–Siris syndrome—Case report

Frontiers in psychiatry, 2023-08, Vol.14

2023

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Substitution rate and natural selection in parvovirus B19

Scientific reports, 2016-10, Vol.6 (1), p.35759-35759, Article 35759

2016

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Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in Serbian population

Journal of medical biochemistry, 2020-01, Vol.39 (2), p.199-207

2020

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A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome

European journal of human genetics : EJHG, 2016-08, Vol.24 (9), p.1280-1286

2016

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Psychosexual Functioning Outcome Testing after Hypospadias Repair

Healthcare (Basel), 2020-02, Vol.8 (1), p.32

2020

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Potential of Gentiana lutea for the Treatment of Obesity-associated Diseases

Current pharmaceutical design, 2019-01, Vol.25 (18), p.2071-2076

2019

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Non-Coding RNAs in Preeclampsia-Molecular Mechanisms and Diagnostic Potential

International journal of molecular sciences, 2021-09, Vol.22 (19), p.10652

2021

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Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy–Walker malformation and single ventricle heart

Prenatal diagnosis, 2024-07, Vol.44 (8), p.1008-1011

2024

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Fanconi Anemia Is Characterized by Delayed Repair Kinetics of DNA Double-Strand Breaks

The Tohoku Journal of Experimental Medicine, 2010, Vol.221(1), pp.69-76

2010

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Telomere fragility in radiology workers occupationally exposed to low doses of ionising radiation

Arhiv za higijenu rada i toksikologiju, 2022-04, Vol.73 (1), p.23-30

2022

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Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability

The journal of histochemistry and cytochemistry, 2020-04, Vol.68 (4), p.239-251

2020

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Assessment of single nucleotide polymorphisms in screening 52 DNA repair and cell cycle control genes in Fanconi anemia patients

Genetika (Beograd), 2015, Vol.47 (2), p.695-710

2015

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Placenta-specific plasma miR518b is a potential biomarker for preeclampsia

Clinical biochemistry, 2020-05, Vol.79, p.28-33

2020

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Management of vaginoplasty canal complications

Current opinion in urology, 2024-09, Vol.34 (5), p.336-343

2024

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Expression analysis of microRNAs and cytokine mRNAs in pregnancies complicated by gestational hypertension

European journal of obstetrics & gynecology and reproductive biology, 2024-10, Vol.301, p.64-69

2024

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Accurate diagnostics of ataxia-telangiectasia cellular phenotype by employing in vitro lymphocyte radiosensitivity testing

Nuclear technology & radiation protection, 2013-06, Vol.28 (2), p.221-224

2013

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Vitamin B12 Reduces Ribavirin-Induced Genotoxicity in Phytohemaglutinin-Stimulated Human Lymphocytes

The Tohoku Journal of Experimental Medicine, 2006, Vol.209(4), pp.347-354

2006

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Expression of miRNAs and proinflammatory cytokines in pregnant women with gestational diabetes mellitus

Journal of reproductive immunology, 2024-03, Vol.162, p.104211-104211, Article 104211

2024

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Increased oxidative stress and cytokinesis-block micronucleus cytome assay parameters in pregnant women with gestational diabetes mellitus and gestational arterial hypertension

Reproductive toxicology (Elmsford, N.Y.), 2017-08, Vol.71, p.55-62

2017

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Optimization of the method for isolation of epithelial cells from the non-glandular part of the rat stomach for flow cytometry

Veterinarski arhiv, 2020-09, Vol.90 (5), p.517-525

2020

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Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter)

Vojnosanitetski pregled, 2020, Vol.77 (7), p.754-757

2020

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Metoidioplasty

Isolated Male Epispadias Repair: Long-Term Outcomes

Small supernumerary marker chromosomes in prenatal diagnosis-molecular characterization and clinical outcomes

Autism spectrum disorder and Coffin–Siris syndrome—Case report

Substitution rate and natural selection in parvovirus B19

Combined presence of coagulation factor XIII V34L and plasminogen activator inhibitor 1 4G/5G gene polymorphisms significantly contribute to recurrent pregnancy loss in Serbian population

A maternal deletion upstream of the imprint control region 2 in 11p15 causes loss of methylation and familial Beckwith-Wiedemann syndrome

Psychosexual Functioning Outcome Testing after Hypospadias Repair

Potential of Gentiana lutea for the Treatment of Obesity-associated Diseases

Non-Coding RNAs in Preeclampsia-Molecular Mechanisms and Diagnostic Potential

Expanding the phenotypic spectrum of MPDZ gene variants: A case report with prenatally detected Dandy–Walker malformation and single ventricle heart

Fanconi Anemia Is Characterized by Delayed Repair Kinetics of DNA Double-Strand Breaks

Telomere fragility in radiology workers occupationally exposed to low doses of ionising radiation

Long-term Culture of EBV-induced Human Lymphoblastoid Cell Lines Reveals Chromosomal Instability

Assessment of single nucleotide polymorphisms in screening 52 DNA repair and cell cycle control genes in Fanconi anemia patients

Placenta-specific plasma miR518b is a potential biomarker for preeclampsia

Management of vaginoplasty canal complications

Expression analysis of microRNAs and cytokine mRNAs in pregnancies complicated by gestational hypertension

Accurate diagnostics of ataxia-telangiectasia cellular phenotype by employing in vitro lymphocyte radiosensitivity testing

Vitamin B12 Reduces Ribavirin-Induced Genotoxicity in Phytohemaglutinin-Stimulated Human Lymphocytes

Expression of miRNAs and proinflammatory cytokines in pregnant women with gestational diabetes mellitus

Combined NGS Approaches Identify Mutations in the Intraflagellar Transport Gene IFT140 in Skeletal Ciliopathies with Early Progressive Kidney Disease

Increased oxidative stress and cytokinesis-block micronucleus cytome assay parameters in pregnant women with gestational diabetes mellitus and gestational arterial hypertension

Optimization of the method for isolation of epithelial cells from the non-glandular part of the rat stomach for flow cytometry

Prenatal ultrasonographic manifestations of partial trisomy 12q(12q24.2→qter) and partial monosomy 2q (2q37.3→qter)

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