about
The role of TPA I/D and PAI-1 4G/5G polymorphisms in multiple sclerosis.Identification of rare genetic variation of NLRP1 gene in familial multiple sclerosis.Functional polymorphisms of matrix metalloproteinases 1 and 9 genes in women with spontaneous preterm birthGenetic heritage of Croatians in the Southeastern European gene pool-Y chromosome analysis of the Croatian continental and Island population.Altered LINE-1 Methylation in Mothers of Children with Down Syndrome.The -2549 insertion/deletion polymorphism in the promoter region of the VEGFA gene in couples with idiopathic recurrent spontaneous abortionPrenatal diagnosis of complete trisomy 19q.Tumor necrosis factor-alpha gene promoter -308 and -238 polymorphisms in patients with lung cancer as a second primary tumorFunctional inference of methylenetetrahydrofolate reductase gene polymorphisms on enzyme stability as a potential risk factor for Down syndrome in Croatia.The lack of association between angiotensin-converting enzyme gene insertion/deletion polymorphism and nicotine dependence in multiple sclerosis.Y chromosome azoospermia factor region microdeletions are not associated with idiopathic recurrent spontaneous abortion in a Slovenian population: association study and literature review.A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses.Insertion/deletion polymorphism in intron 16 of ACE gene in idiopathic recurrent spontaneous abortion: case-control study, systematic review and meta-analysis.Systematic review and meta-analysis of genetic association studies in idiopathic recurrent spontaneous abortion.Angiotensin-converting enzyme insertion/deletion gene polymorphism in multiple sclerosis: a meta-analysis.Genetic variation in tissue inhibitors of metalloproteinases as a risk factor for idiopathic recurrent spontaneous abortion.Mutations in the hemochromatosis gene (HFE) and multiple sclerosis.Angiotensin-converting enzyme insertion/deletion gene polymorphism in lung cancer patients.Secular change in body height and cephalic index of Croatian medical students (University of Rijeka).Angiotensin-converting enzyme insertion/deletion gene polymorphism and interferon-β treatment response in multiple sclerosis patients: a preliminary report.The insertion/deletion polymorphism in the angiotensin-converting enzyme gene and nicotine dependence in schizophrenia patients.Functional single nucleotide polymorphisms of matrix metalloproteinase 7 and 12 genes in idiopathic recurrent spontaneous abortion.Severe psychomotor retardation in a boy with a small supernumerary marker chromosome 19p.Association of circadian rhythm genes ARNTL/BMAL1 and CLOCK with multiple sclerosis.Genetic predisposition to idiopathic recurrent spontaneous abortion: contribution of genetic variations in IGF-2 and H19 imprinted genes.Secular change of craniofacial measures in Croatian younger adults.Matrix metalloproteinases 1, 2, 3 and 9 functional single-nucleotide polymorphisms in idiopathic recurrent spontaneous abortion.The insulin-like growth factor 2 receptor gene Gly1619Arg polymorphism and idiopathic recurrent spontaneous abortion.Genetic polymorphisms of 15 STR loci in the population of the island of Cres (Croatia).Angiotensin-converting enzyme I/D gene polymorphism and risk of multiple sclerosis.Human Y-specific STR haplotypes in the Western Croatian population sample.Third case of 8q23.3-q24.13 deletion in a patient with Langer-Giedion syndrome phenotype without TRPS1 gene deletion.CTLA-4 +49 A/G gene polymorphism in Croatian and Slovenian multiple sclerosis patientsBanI polymorphism of cytosolic phospholipase A2 gene is associated with age at onset in male patients with schizophrenia and schizoaffective disorderSex-specific differences of craniofacial traits in Croatia: The impact of environment in a small geographic areaChromosomal anomalies in abnormal human pregnanciesThe influence of smoking and parity on serum markers for Down's syndrome screeningScreening for Down's syndrome and neural tube defect in Croatia. A regional prospective studyHemochromatosis gene mutations in the Croatian and Slovenian populationsTumor necrosis factor-alpha-308 gene polymorphism in Croatian and Slovenian multiple sclerosis patients
P50
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P50
description
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Miljenko Kapović
@ast
Miljenko Kapović
@en
Miljenko Kapović
@es
Miljenko Kapović
@nl
type
label
Miljenko Kapović
@ast
Miljenko Kapović
@en
Miljenko Kapović
@es
Miljenko Kapović
@nl
prefLabel
Miljenko Kapović
@ast
Miljenko Kapović
@en
Miljenko Kapović
@es
Miljenko Kapović
@nl
P214
P106
P1153
6603836708
P214
P31
P496
0000-0002-8466-1011
P7859
viaf-305498151