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Volume 21 (2018): Issue 2 (Dec 2018)

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

13 articles
Open Access
|Dec 2018
Investigation of circulating serum microRNA-328-3p and microRNA-3135a expression as promising novel biomarkers for autism spectrum disorder
NT Popov,  DS Minchev,  MM Naydenov,  IN Minkov and  TI Vachev  
Open Access
|Dec 2018
Determining specific thyroid transcripts in peripheral blood: A single center study experience
T Makazlieva,  A Eftimov,  O Vaskova,  T Tripunoski,  D Miladinova,  S Risteski,  H Jovanovic and  Z Jakovski  
Open Access
|Dec 2018
The frequency of EGFR And KRAS mutations in the Turkish population with non-small cell lung cancer and their response to erlotinib therapy
A Demiray,  A Yaren,  N Karagenç,  F Bir,  AG Demiray,  ER Karagür,  O Tokgün,  L Elmas and  H Akça  
Open Access
|Dec 2018
Epigenetic signature of chronic maternal stress load during pregnancy might be a potential biomarker for spontaneous preterm birth
M Rogac and  B Peterlin  
Open Access
|Dec 2018
Characteristic diagnostic clues of metatropic dysplasia: The lumbothoracic humpback with dumbbell appearance of the long bones
Z Gucev,  G Kalcev,  N Laban,  Z Bozinovski,  N Popovski,  A Saveski,  B Daskalov,  D Plaseska-Karanfilska and  V Tasic  
Open Access
|Dec 2018
Myotonic dystrophy-2: Unusual phenotype due to a small CCTG-expansion
J Finsterer,  C Stöllberger,  A Reining-Festa,  M Loewe-Grgurin and  M Gencik  
Open Access
|Dec 2018
Next generation sequencing identified a novel multi exon deletion of the NF1 gene in a Chinese pedigree with neurofibromatosis type 1
J Yang,  J-X An,  X-L Liu,  Z-Q Wang,  G-M Xie,  X-L Yang,  S-J Xu,  F Feng and  Y Ni  
Open Access
|Dec 2018
The role of next generation sequencing in the differential diagnosis of caroli’s syndrome
B Smolović,  D Muhović,  A Hodžić,  G Bergant and  B Peterlin  
Open Access
|Dec 2018
A novel mutation in a newborn baby leading to glycogen storage disease type Ia
S Dorum and  O Gorukmez  
Open Access
|Dec 2018
Rare case of a heterozygous microdeletion 9q21.11-q21.2: Clinical and genetic characteristics
HY Ivanov,  V Stoyanova,  I Ivanov,  A Linev,  R Vazharova,  S Ivanov,  L Balabanski and  D Toncheva  
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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