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Volume 25 (2022): Issue 1 (Jun 2022)

Open Access
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Balkan Journal of Medical Genetics
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Issue 2 (December 2022)
Issue 1 (June 2022)

14 articles
Open Access
|Mar 2023
“We’ve opened pandora’s box, haven’t we?” clinical geneticists’ views on ethical aspects of genomic testing in neonatal intensive care
T Arsov  
Open Access
|Mar 2023
APOE4 Status and cognitive function in middle-aged and elderly people
N.A. Pavel,  M.R. Paun,  P.V. Matei,  I. Dutu and  C. Tudose  
Open Access
|Mar 2023
Comprehensive genetic evaluation of Bulgarian children with syndromic craniosynostosis
T Delchev,  S Hadjidekova,  S Bichev,  Ts Veleva,  I Boneva and  D Avdjieva-Tzavella  
Open Access
|Mar 2023
Identification of key target genes and pathway analysis in nonalcoholic fatty liver disease via integrated bioinformatics analysis
X. Chen,  L. Zhang,  Y. Wang,  R. Li,  M. Yang and  L. Gao  
Open Access
|Mar 2023
Matrix metalloproteinase-2 (MMP-2 ) and-9 (MMP-9) gene variants and microvascular complications in type 2 diabetes patients
Jelic M Andjelic,  D Radojkovic,  A Nikolic,  Lj Rakicevic,  T Babic,  D Jelic and  NM Lalic  
Open Access
|Mar 2023
Vitamin D receptor polymorphisms among the Turkish population are associated with multiple sclerosis
B Bulan,  AY Hoscan,  SN Keskin,  A Cavus,  EA Culcu,  N Isik,  EO List and  A Arman  
Open Access
|Mar 2023
Single nucleotide polymorphisms in IL-1A RS1800587, IL-1B RS1143634 and vitamin D receptor rs731236 in stage III grade B/C periodontitis
Özener H. Özturk,  Aslan B. Tacal,  B.F. Eken,  Ö.B. Agrali,  H.S. Yildrim,  E.Ç. Altunok,  K. Ulucan and  L. Kuru  
Open Access
|Mar 2023
MIR-147B regulated proliferation and apoptosis of gastric cancer cells by targeting CPEB2 via the PTEN pathway
Tao К,  J-H. Dong,  D. Wang,  F. Li and  Z-T. Zhang  
Open Access
|Mar 2023
A novel Loss-of-function Mutation in MYBPC3 Causes familial hypertrophic cardiomyopathy with extreme intrafamilial phenotypic heterogeneity
Y Peng,  J Xu,  Y Wang,  J Zhao,  L Zhang,  Z Chen,  Y Jiang,  S Banerjee,  Z Zhang and  M Bai  
Open Access
|Mar 2023
Keratitis-ichthyosis-deafness syndrome with heterozygous p.D50N in the GJB2 gene in two Serbian adult patients
T Kalezić,  I Vuković,  M Stojković,  S Stanojlović,  J Karanović,  G Brajušković and  D Savić-Pavićević  
eISSN: 2199-5761|Language: English|Publication frequency: 2 times per year
Published by: Macedonian Academy of Sciences and Arts
In partnership with: Paradigm Publishing Services
Related subjects:
Medicine,
Basic medical science,
Basic medical science, other
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