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Balkan Journal of Medical Genetics
Volume 21 (2018): Issue 1 (June 2018)
Volume 21 (2018): Issue 1 (Jun 2018)
Balkan Journal of Medical Genetics
Open Access
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Volume 28 (2025)
Volume 27 (2024)
Volume 26 (2023)
Volume 25 (2022)
Volume 24 (2021)
Volume 23 (2020)
Volume 22 (2019)
Volume 21 (2018)
Issue 2 (December 2018)
Issue 1 (June 2018)
Volume 20 (2017)
Volume 19 (2016)
Volume 18 (2015)
Volume 17 (2014)
Volume 16 (2013)
Volume 15 (2012)
Volume 14 (2011)
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14 articles
Open Access
|
Oct 2018
Abstract
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
Abstract
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
Abstract
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
Abstract
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
Abstract
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
Abstract
PPAR𝛾 gene and atherosclerosis: Genetic polymorphisms, epigenetics and therapeutic implications
E Grbić
,
A Peterlin
,
T Kunej
and
D Petrovič
Open Access
|
Oct 2018
Abstract
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
Abstract
The mitochondrial tRNAGly T10003C mutation may not be associated with diabetes mellitus
Q Yuan
,
ZG Zhao
and
HJ Yuan
Open Access
|
Oct 2018
Abstract
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
Abstract
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
1
2
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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