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Volume 21 (2018): Issue 1 (Jun 2018)

Open Access
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Balkan Journal of Medical Genetics
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Issue 2 (December 2018)
Issue 1 (June 2018)

14 articles
Open Access
|Oct 2018
Family history as an important factor for stratifying participants in genetic studies of major depression
B Zalar,  A Blatnik,  A Maver,  Z Klemenc-Ketiš and  B Peterlin  
Open Access
|Oct 2018
Detecting EGFR mutations in patients with non-small cell lung cancer
ZA Hammoudeh,  O Antonova,  R Staneva,  D Nikolova,  Y Kyuchukov,  A Penev,  T Mintchev,  V Koleva,  S Hadjidekova and  D Toncheva  
Open Access
|Oct 2018
Analysis of the PPARD gene expression level changes in football players in response to the training cycle
D Domańska-Senderowska,  A Snochowska,  P Szmigielska,  Z Jastrzębski,  A Jegier,  J Kiszałkiewicz,  K Dróbka,  J Jastrzębska,  D Pastuszak-Lewandoska,  P Cięszczyk,  A Maciejewska-Skrendo,  P Zmijewski and  E Brzeziańska-Lasota  
Open Access
|Oct 2018
Association of E-selectin S128R polymorphism with hereditary breast carcinoma susceptibility in Turkish patients without BRCA1/2 germline mutations
K Yararbas and  PB Atalay  
Open Access
|Oct 2018
ADRB2 gene polymorphisms and salbutamol responsiveness in Serbian children with asthma
N Jovicic,  T Babic,  S Dragicevic,  B Nestorovic and  A Nikolic  
Open Access
|Oct 2018
PPAR𝛾 gene and atherosclerosis: Genetic polymorphisms, epigenetics and therapeutic implications
E Grbić,  A Peterlin,  T Kunej and  D Petrovič  
Open Access
|Oct 2018
Clinical variability in two Macedonian families with Arterial tortuosity syndrome
M Kocova,  R Kacarska,  K Kuzevska-Maneva,  S Prijic,  M Lazareska,  C Dordoni,  M Ritelli and  M Colombi  
Open Access
|Oct 2018
The mitochondrial tRNAGly T10003C mutation may not be associated with diabetes mellitus
Q Yuan,  ZG Zhao and  HJ Yuan  
Open Access
|Oct 2018
UGT1A1 (TA)n promoter genotype: Diagnostic and population pharmacogenetic marker in Serbia
M Vukovic,  N Radlovic,  Z Lekovic,  K Vucicevic,  N Maric,  N Kotur,  V Gasic,  M Ugrin,  M Stojiljkovic,  L Dokmanovic,  B Zukic and  S Pavlovic  
Open Access
|Oct 2018
Mutation in Phospholipase C, δ1 (PLCD1) gene underlies hereditary leukonychia in a Pashtun family and review of the literature
AK Khan,  SA Khan,  Na Muhammad,  No Muhammad,  J Ahmad,  H Nawaz,  A Nasir,  S Farman and  S Khan  
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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