Претрага
Резултати
Chromosomal Variants in Klinefelter Syndrome
[2019]
Đorđević, Vesna R.; Jovanović, Jelica V.; Denčić-Fekete, Marija Study of TNF, IL1B, and IL6 genes polymorphisms and susceptibility to bronchopulmonary dysplasia in premature neonates
[2019]
Damnjanović, Tatjana M. GSTM! gene deletion as potential indicator of risk of childhood [2013]
R Milicevic; Lj Popovic; Lj Brankovic; Stamenković, HristinaRare case of androgenetic-biparental mosacism causing placental mesenchymal dysplasia [2024]
Joksic, Ivana D; Toljic, Mina; Milovanovic, Zagorka M; Dzuverovic, Marko; Stankovic, Andjela S; Mikovic, Zeljko MPolymorphism of the MTHFR gene and serum lipid levels in Serbian child population
[2005]
Damnjanović, Tatjana Analysis of ACE and eNOS gene polymorphism in hemodialysis patients
[2008]
Damnjanović, Tatjana Novel HSPB8 mutations in severe early-onset myopathy with involvement of respiratory and cardiac muscles cause proteostasis defects in cell models
[2025]
Tedesco, Barbara; Perić, Stojan RET oncogene mutations in Serbian patients with thyroid medullary carcinoma [2002]
Neskovic, GGStudy of the polymorphisms in genes IL-17, IL-23, TGFb, RORgT and FOXP3 in Serbian patients with antiphospholipid syndrome
[2018]
Novaković, Ivana V. Determination of the phylogenetic origins of the arpad Dynasty based on Y chromosome sequencing of Bela the Third [2021]
Nagy, Peter L; ...; Zgonjanin, Dragana M; ...; (broj, koautora 23)Филтери
По типу
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