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Volume 22 (2019): Issue 2 (Nov 2019)

Open Access
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Balkan Journal of Medical Genetics
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Issue 2 (November 2019)
Issue 1 (June 2019)

14 articles
Open Access
|Dec 2019
Molecular basis of inherited colorectal carcinomas in the Macedonian population: An update
M Staninova-Stojovska,  N Matevska-Geskovska,  M Panovski,  B Angelovska,  N Mitrevski,  M Ristevski,  R Jovanovic and  AJ Dimovski  
Open Access
|Dec 2019
Results of liquid biopsy studies by next generation sequencing in patients with advanced stage non-small cell lung cancer: Single center experience from Turkey
M Buyuksimsek,  M Togun,  Kara I Oguz,  A Bisgin,  I Boga,  M Tohumcuoglu,  A Ogul,  Yetisir A Evren,  B Sahin,  HE Sumbul and  C Mirili  
Open Access
|Dec 2019
TWIST1 Gene expression as a biomarker for predicting primary doxorubicin resistance in breast cancer
S Demir,  MH Müslümanoğlu,  M Müslümanoğlu,  S Başaran,  ZZ Çalay,  A Aydıner,  U Vogt,  T Çakır,  H Kadıoğlu and  S Artan  
Open Access
|Dec 2019
Evaluation of the JAK2V617F mutational burden in patients with philadelphia chromosome negative myeloproliferative neoplasms: A single-center experience
M Popova-Labachevska,  I Panovska-Stavridis,  A Eftimov,  Nestorovska A Kapedanovska,  L Cevreska,  M Ivanovski,  N Ridova,  S Trajkova and  AJ Dimovski  
Open Access
|Dec 2019
Association of variants in the CP, ATOX1 and COMMD1 genes with Wilson disease symptoms in Latvia
A Zarina,  I Tolmane,  Z Krumina,  AI Tutane and  L Gailite  
Open Access
|Dec 2019
Association of genetic polymorphisms in the Matrix Gla Protein (MGP) gene with coronary artery disease and serum mgp levels
S Karsli-Ceppioglu,  S Yazar,  Y Keskin,  M Karaca,  NE Luleci and  T Yurdun  
Open Access
|Dec 2019
Chronic obstructive pulmonary disease risk and smoking cessation changes induced by CHRNA5-A3 and CHRNB3-A6 variation in a Chinese male population
L Zhao,  L-Y Zou,  B-F Cheng,  X-J Yu,  J-H Zou and  W Han  
Open Access
|Dec 2019
Association of VDR gene variant (rs1544410) with type 2 diabetes in a Pakistani cohort
A Khan,  S Khan,  A Aman,  Y Ali,  M Jamal,  B Rahman,  M Ahmad,  M Aasim,  F Jalil and  AA Shah  
Open Access
|Dec 2019
Clinical next generation sequencing reveals an H3F3A gene as a new potential gene candidate for microcephaly associated with severe developmental delay, intellectual disability and growth retardation
A Maver,  G Čuturilo,  Stojanović J Ruml and  B Peterlin  
Open Access
|Dec 2019
Novel genotype in two siblings with 5-α-reductase 2 deficiency: Different clinical course due to the time of diagnosis
M Kocova,  D Plaseska-Karanfilska,  P Noveski and  M Kuzmanovska  
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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