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GENETIC CAUSES OF MALE INFERTILITY; KARYOTYPING AND Y MICRODELETION ANALYSIS.
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- Genetics & Applications, 2024, p. 18
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- Article
APPLICATION OF MOLECULAR KARYOTYPING IN PRENATAL DIAGNOSTICS.
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- Genetics & Applications, 2024, p. 17
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- Article
POLYMORPHISMS OF 5,10-METHYLENETETRAHYDROFOLATE REDUCTASE GENE IN MULTIPLE SCLEROSIS.
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- Genetics & Applications, 2023, p. 57
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- Article
RARE RECIPROCAL TRANSLOCATION IN A PATIENT WITH ASTHENOZOOSPERMIA: CASE REPORT.
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- Genetics & Applications, 2023, p. 20
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- Article
Tumor Necrosis Factor-α-308 Gene Polymorphism in Croatian and Slovenian Multiple Sclerosis Patients.
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- European Neurology, 2007, v. 57, n. 4, p. 203, doi. 10.1159/000099159
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- Article
Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.
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- PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0190601
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- Article
The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis.
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- Brain & Behavior, 2017, v. 7, n. 1, p. n/a, doi. 10.1002/brb3.600
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- Article
GiOPARK Project: The Genetic Study of Parkinson's Disease in the Croatian Population.
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- Genes, 2024, v. 15, n. 2, p. 255, doi. 10.3390/genes15020255
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- Article
CCR5 Δ32 and CTLA-4 +49 A/G Gene Polymorphisms and Interferon-β Treatment Response in Croatian and Slovenian Multiple Sclerosis Patients.
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- International Journal of Molecular Sciences, 2024, v. 25, n. 13, p. 7412, doi. 10.3390/ijms25137412
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- Article
LETTER TO THE EDITOR.
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- Croatian Medical Journal, 2021, v. 62, n. 3, p. 305, doi. 10.3325/cmj.2021.62.305
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- Article
Does the CCR5-Δ32 mutation explain the variable coronavirus-2019 pandemic statistics in Europe?
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- 2020
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- Letter to the Editor
Frequency of CCR5 Gene 32-Basepair Deletion in Croatian Normal Population.
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- Croatian Medical Journal, 2005, v. 46, n. 4, p. 693
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- Article
Applicability of clinical genetic testing for deep brain stimulation treatment in monogenic Parkinson's disease and monogenic dystonia: a multidisciplinary team perspective.
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- Frontiers in Neuroscience, 2023, p. 1, doi. 10.3389/fnins.2023.1282267
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- Article
Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis.
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- 2016
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- journal article
Lack of association between C282Y and H63D polymorphisms in the hemochromatosis gene and risk of multiple sclerosis: A meta-analysis.
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- Biomedical Reports, 2022, v. 16, n. 2, p. 1, doi. 10.3892/br.2021.1495
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- Article
Potential protective role of a NOD2 polymorphism in the susceptibility to multiple sclerosis is not associated with interferon therapy.
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- Biomedical Reports, 2021, v. 15, n. 6, p. N.PAG, doi. 10.3892/br.2021.1476
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- Article
The Influence of Hemochromatosis Gene (HFE) Mutations on SARSCoV- 2 Susceptibility and COVID-19 Severity.
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- Balkan Medical Journal, 2023, v. 40, n. 3, p. 229, doi. 10.4274/balkanmedj.galenos.2023.2023-1-39
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- Article
Geni i celijakija.
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- Paediatria Croatica, 2015, v. 59, n. 2, p. 88, doi. 10.13112/PC.2015.14
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- Article
Could angiotensin-converting enzyme 1 I/D polymorphism be a modificator of COVID-19 response in different populations, diseases, and/or conditions?
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- Journal of the Renin-Angiotensin-Aldosterone System, 2020, v. 21, n. 3, p. 1, doi. 10.1177/1470320320957157
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- Article
Could the CCR5-Δ32 Mutation be Protective in SARS-CoV-2 Infection?
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- Physiological Research, 2021, v. 70, p. S249, doi. 10.33549/physiolres.934725
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- Article
The Role of TPAI/D and PAI-1 4G/5G Polymorphisms in Multiple Sclerosis.
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- Disease Markers, 2014, p. 1, doi. 10.1155/2014/362708
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- Article
Functional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia.
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- Disease Markers, 2010, v. 28, n. 5, p. 293, doi. 10.3233/DMA-2010-0704
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- Article
HLA-DQA1 i HLADQB1 geni u pacijenata s celijakijom.
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- Medicina Fluminensis, 2016, v. 52, n. 1, p. 87
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- Article
MTHFR C677T and A1298C polymorphisms as a risk factor for congenital heart defects in Down syndrome.
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- Pediatrics International, 2011, v. 53, n. 4, p. 546, doi. 10.1111/j.1442-200X.2010.03310.x
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- Article
Interleukin 7 receptor alpha polymorphism rs6897932 and susceptibility to multiple sclerosis in the Western Balkans.
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- Multiple Sclerosis (13524585), 2010, v. 16, n. 5, p. 533, doi. 10.1177/1352458509360548
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- Article
PAI and TPA gene polymorphisms in multiple sclerosis.
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- Multiple Sclerosis (13524585), 2008, v. 14, n. 2, p. 243
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- Article
No association of CCR5Δ32 gene mutation with multiple sclerosis in Croatian and Slovenian patients.
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- Multiple Sclerosis (13524585), 2006, v. 12, n. 3, p. 360, doi. 10.1191/135248506ms1305sr
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- Article