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Journals
Balkan Journal of Medical Genetics
Volume 20 (2017): Issue 2 (December 2017)
Open Access
Balkan Journal of Medical Genetics
Volume 20 (2017): Issue 2 (December 2017)
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14 Articles
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Original Article
Open Access | Dec 29, 2017
Detection of allelic variants of the
POLE
and
POLD1
genes in colorectal cancer patients
LA Pätzold
LA Pätzold
,
D Bērziņa
D Bērziņa
,
Z Daneberga
Z Daneberga
,
J Gardovskis
J Gardovskis
and
E Miklaševičs
E Miklaševičs
Open Access | Dec 29, 2017
Differential expression of FGFRs signaling pathway components in bladder cancer: A step toward personalized medicine
Z Ousati Ashtiani
Z Ousati Ashtiani
,
J Tavakkoly-Bazzaz
J Tavakkoly-Bazzaz
,
SA Salami
SA Salami
,
MR Pourmand
MR Pourmand
,
F Mansouri
F Mansouri
,
R Mashahdi
R Mashahdi
and
G Pourmand
G Pourmand
Open Access | Dec 29, 2017
Superoxide dismutase 1
and
2
gene polymorphism in Turkish vitiligo patients
A Tuna
A Tuna
,
G Ozturk
G Ozturk
,
TB Gerceker
TB Gerceker
,
E Karaca
E Karaca
,
H Onay
H Onay
,
SM Guvenc
SM Guvenc
and
O Cogulu
O Cogulu
Open Access | Dec 29, 2017
Association of the MMP7 –181A>G promoter polymorphism with early onset of chronic obstructive pulmonary disease
T Tacheva
T Tacheva
,
D Dimov
D Dimov
,
A Anastasov
A Anastasov
,
Y Zhelyazkova
Y Zhelyazkova
,
M Kurzawski
M Kurzawski
,
M Gulubova
M Gulubova
,
M Drozdzik
M Drozdzik
and
T Vlaykova
T Vlaykova
Open Access | Dec 29, 2017
Increased frequency of
MEFV
genes in patients with epigastric pain syndrome
BD Coskun
BD Coskun
,
A Kiraz
A Kiraz
,
E Sevinc
E Sevinc
,
O Baspinar
O Baspinar
and
E Cakmak
E Cakmak
Open Access | Dec 29, 2017
The mitochondrial COI/tRNA
SER(UCN)
G7444A mutation may be associated with hearing impairment in a Han Chinese family
Y Ding
Y Ding
,
B-H Xia
B-H Xia
,
Y-S Teng
Y-S Teng
,
G-C Zhuo
G-C Zhuo
and
J-H Leng
J-H Leng
Open Access | Dec 29, 2017
Polymorphism of the
ADRB2
rs1042713 gene is not associated with spontaneous preterm birth: Analyses in a Slovenian sample and meta analysis
A Peterlin
A Peterlin
,
A Maver
A Maver
,
Z Jan
Z Jan
,
L Lovrecic
L Lovrecic
,
N Tul
N Tul
and
B Peterlin
B Peterlin
Open Access | Dec 29, 2017
Association between Osteoprotegerin gene polymorphisms and risk of coronary artery disease: A systematic review and meta-analysis
P Jia
P Jia
,
N Wu
N Wu
,
D Jia
D Jia
and
Y Sun
Y Sun
Open Access | Dec 29, 2017
Molecular characterization of iranian patients with inherited coagulation factor VII deficiency
S Shahbazi
S Shahbazi
,
R Mahdian
R Mahdian
,
K Karimi
K Karimi
and
A Mashayekhi
A Mashayekhi
Open Access | Dec 29, 2017
Association between inherited thrombophilia in pregnancy and micronucleus frequency in peripheral blood lymphocytes
GM Šošić
GM Šošić
,
N Jović
N Jović
,
B Rakić
B Rakić
,
A Dimitrijević
A Dimitrijević
and
M Varjačić
M Varjačić
Open Access | Dec 29, 2017
Association of placenta previa with a history of previous Cesarian deliveries and indications for a possible role of a genetic component
M Matalliotakis
M Matalliotakis
,
A Velegrakis
A Velegrakis
,
GN Goulielmos
GN Goulielmos
,
E Niraki
E Niraki
,
AE Patelarou
AE Patelarou
and
I Matalliotakis
I Matalliotakis
Letter to the Editor
Open Access | Dec 29, 2017
Female and male carriers of
TAZ
mutations need to be thoroughly investigated
J Finsterer
J Finsterer
,
C Stollberger
C Stollberger
,
M Bakšienė
M Bakšienė
,
E Benušienė
E Benušienė
,
A Morkūnienė
A Morkūnienė
,
L Ambrozaitytė
L Ambrozaitytė
,
A Utkus
A Utkus
and
V Kučinskas
V Kučinskas
Open Access | Dec 29, 2017
Epidermal growth factor receptor
Mutation status: Does younger mean more frequently mutated?
P Wójcik
P Wójcik
,
P Krawczyk
P Krawczyk
,
J Chorostowska-Wynimko
J Chorostowska-Wynimko
,
K Reszka
K Reszka
,
K Duk
K Duk
,
B Muszczyńska-Bernhard
B Muszczyńska-Bernhard
,
J Pankowski
J Pankowski
,
K Wojas-Krawczyk
K Wojas-Krawczyk
,
G Czyżewicz
G Czyżewicz
,
R Ramlau
R Ramlau
,
M Skoczek
M Skoczek
,
A Grenda
A Grenda
,
T Orłowski
T Orłowski
,
T Grodzki
T Grodzki
,
M Piwowar
M Piwowar
,
K Roszkowski-Śliż
K Roszkowski-Śliż
and
J Milanowski
J Milanowski
Case Report
Open Access | Dec 29, 2017
Galactosialidosis in a newborn with a novel mutation in the
CTSA
gene presenting with transient hyperparathyroidism
E Okulu
E Okulu
,
G Tunc
G Tunc
,
T Eminoglu
T Eminoglu
,
O Erdeve
O Erdeve
,
B Atasay
B Atasay
and
S Arsan
S Arsan
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