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Volume 26 (2023): Issue 2 (Dec 2023)

Open Access
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Balkan Journal of Medical Genetics
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Issue 2 (December 2023)
Issue 1 (July 2023)

12 articles
Open Access
|Mar 2024
Preimplantation Genetic Testing within the Public Healthcare System in Slovenia
M Volk,  K Writzl,  A Veble,  H Jaklič,  N Teran,  B Prosenc,  M Štimpfel,  I Virant Klun,  E Vrtačnik Bokal,  H Ban Frangež and  B Peterlin  
Open Access
|Mar 2024
Chromosomal Abnormalities in Early Pregnancy Losses: A Study of 900 Samples
Gj Bozhinovski,  M Terzikj,  K Kubelka-Sabit,  Dz Jasar,  S Lazarevski,  V Livrinova and  D Plaseska-Karanfilska  
Open Access
|Mar 2024
Droplet Digital PCR as a Molecular Tool for the Detection of the EGFR T790M Mutation in NSCLC Patients with the EGFR Activating Mutations
S Durgut,  L Salihefendić,  D Pećar,  I Čeko,  N Mulahuseinović,  M Izmirlija and  R Konjhodžić  
Open Access
|Mar 2024
Association Between the Polymorphism of Angiotensin-Converting Enzyme Gene and Interleukin-1 Beta Gene and the Response to Erythropoietin Therapy in Dialysis Patients with Anemia
P Dzekova-Vidimliski,  N Eftimovska-Otovikj,  I G Nikolov,  Gj Selim,  I Rambabova-Bushljetik,  V Pushevski,  V Karanfilovski,  N Matevska-Geshovska and  A Dimovski  
Open Access
|Mar 2024
Co-Existence of CYP2C19*1/*2 and ABCB1c.3435 CT Genotype has a Potential Impact on Clinical Outcome in CAD Patients Treated with Clopidogrel
KA Nestorovska,  Z Naumovska,  M Staninova Stojovska,  Z Sterjev,  A Dimovski and  Lj Suturkova  
Open Access
|Mar 2024
Determination of the Relationship Between DNA Methylation Status of KLOTHO and ARNTL Genes With Hypertension
M Osum,  O Tosun,  H Birtan and  R Kalkan  
Open Access
|Mar 2024
Do Gene Polymorphisms Play a Role in Newborn Hyperbilirubinemia?
N Hakan,  M Aydin,  S Ceylaner,  D Dilli,  A Zenciroğlu and  N Okumuş  
Open Access
|Mar 2024
Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21
A Paripović,  A Maver,  N Stajić,  J Putnik,  S Ostojić,  B Alimpić,  N Ilić and  A Sarajlija  
Open Access
|Mar 2024
EPHA4 Genetic Variant in a Patient with Epilepsy, Ophthalmological Anomalies, and Neurodevelopmental Delay
M Sleptsova,  C Georgiev,  S Atemin,  P Dimova,  D Avdjieva-Tzavella,  G Tacheva,  I Litvinenko,  L Grozdanova,  T Todorov,  V Mitev and  A Todorova  
Open Access
|Mar 2024
Misdiagnosis of Tracher-Collins Syndrome Initially Attributed to Drug Teratogenicity: A Moroccan Case Report
A Lamzouri,  A EL Rherbi,  I Ratbi,  FZ Laarabi,  R Chahboune,  SC Elalaoui,  H Hamdaoui,  RS Bencheikh and  A Sefiani  
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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