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Balkan Journal of Medical Genetics

Tom 20 (2017): Zeszyt 1 (Czerwiec 2017)

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12 Artykułów

Original Article

Otwarty dostęp | 30 cze 2017
Analysis of the mitochondrial 4977 bp deletion in patients with hepatocellular carcinoma
ZS Guo

ZS Guo

Department of Hepatobiliary Surgery, Zhuji People’s HospitalShaoxing, People’s Republic of China
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Guo, ZS
, 
CL Jin

CL Jin

Department of Endocrinology, Zhuji People’s HospitalShaoxing, People’s Republic of China
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Jin, CL
, 
ZJ Yao

ZJ Yao

Department of Hepatobiliary Surgery, Zhuji People’s HospitalShaoxing, People’s Republic of China
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Yao, ZJ
, 
YM Wang

YM Wang

Department of Hepatobiliary Surgery, Zhuji People’s HospitalShaoxing, People’s Republic of China
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Wang, YM
 oraz 
BT Xu

BT Xu

Department of Cardiothoracic Surgery, Zhuji People’s HospitalShaoxing, People’s Republic of China
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Xu, BT
  
Otwarty dostęp | 30 cze 2017
Effect of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor γ2 gene on lipid profile and adipokines levels in obese subjects
E Becer

E Becer

  • Department of Biochemistry, Faculty of Pharmacy, Near East UniversityNicosia, Turkey
  • Experimental Health Science Research Center, Near East UniversityNicosia, Turkey
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Becer, E
 oraz 
A Çırakoğlu

A Çırakoğlu

Department of Medical Biology, Cerrahpasa Faculty of Medicine, Istanbul UniversityIstanbul, Turkey
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Çırakoğlu, A
  
Otwarty dostęp | 30 cze 2017
Association of the Apolipoprotein A-I gene polymorphisms with cardiovascular disease risk factors and atherogenic indices in patients from assam, Northeast India
K Bora

K Bora

  • Regional Medical Research Centre, Northeast Region, Indian Council of Medical ResearchAssam, India
  • Department of Biochemistry, Gauhati Medical College and HospitalAssam, India
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Bora, K
, 
MS Pathak

MS Pathak

Department of Biochemistry, Gauhati Medical College and HospitalAssam, India
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Pathak, MS
, 
P Borah

P Borah

State Biotech Hub (Assam) and Department of Animal Biotechnology, College of Veterinary ScienceAssam, India
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Borah, P
, 
Md.I Hussain

Md.I Hussain

State Biotech Hub (Assam) and Department of Animal Biotechnology, College of Veterinary ScienceAssam, India
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Hussain, Md.I
 oraz 
D Das

D Das

Regional Nursing CollegeAssam, India
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Das, D
  
Otwarty dostęp | 30 cze 2017
The LRP1 gene polymorphism is associated with increased risk of metabolic syndrome prevalence in the Serbian population
N Vučinić

N Vučinić

University of Novi Sad, Faculty of Medicine, Department of PharmacyNovi Sad, Serbia
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Vučinić, N
, 
E Stokić

E Stokić

  • University of Novi Sad, Faculty of Medicine, Department of PharmacyNovi Sad, Serbia
  • Clinical Center of Vojvodina, Department of Endocrinology, and Metabolic DisordersNovi Sad, Serbia
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Stokić, E
, 
I Djan

I Djan

  • University of Novi Sad, Faculty of MedicineNovi Sad, Serbia
  • Institute of Oncology, Department of RadiotherapySremska Kamenica, Serbia
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Djan, I
, 
D Obreht

D Obreht

University of Novi Sad, Faculty of Sciences, Department of Biolgy and EcologyNovi Sad, Serbia
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Obreht, D
, 
N Veličković

N Veličković

University of Novi Sad, Faculty of Sciences, Department of Biolgy and EcologyNovi Sad, Serbia
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Veličković, N
, 
K Stankov

K Stankov

University of Novi Sad, Faculty of Medicine, Department of BiochemistryNovi Sad, Serbia
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Stankov, K
 oraz 
M Djan

M Djan

University of Novi Sad, Faculty of Sciences, Department of Biolgy and EcologyNovi Sad, Serbia
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Djan, M
  
Otwarty dostęp | 30 cze 2017
Analysis of meiotic segregation patterns and interchromosomal effects in sperm from 13 robertsonian translocations
B Wang

B Wang

Department of Clinical Laboratory, Hubei Maternal and Child Health HospitalWuhan, Hubei, People’s Republic of China
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Wang, B
, 
B Nie

B Nie

Department of Clinical Laboratory, Hubei Maternal and Child Health HospitalWuhan, Hubei, People’s Republic of China
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Nie, B
, 
D Tang

D Tang

Department of Clinical Laboratory, Renmin Hospital Wuhan UniversityWuhan, Hubei, People’s Republic of China
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Tang, D
, 
R Li

R Li

Internal Medicine-Cardiovascular Department, Xiaogan Hospital affiliated to Wuhan University of Science and TechnologyXiaogan, Hubei, People’s Republic of China
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Li, R
, 
X Liu

X Liu

Department of Clinical Laboratory, Hubei Maternal and Child Health HospitalWuhan, Hubei, People’s Republic of China
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Liu, X
, 
J Song

J Song

Department of Clinical Laboratory, Hubei Maternal and Child Health HospitalWuhan, Hubei, People’s Republic of China
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Song, J
, 
W Wang

W Wang

Department of Clinical Laboratory, Hubei Maternal and Child Health HospitalWuhan, Hubei, People’s Republic of China
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Wang, W
 oraz 
Z Liu

Z Liu

Department of Clinical Laboratory, Hubei Maternal and Child Health HospitalWuhan, Hubei, People’s Republic of China
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Liu, Z
  
Otwarty dostęp | 30 cze 2017
Genetic polymorphisms of hemostatic factors and thrombotic risk in non BCR-ABL myeloproliferative neoplasms: A pilot study
R Dambrauskienė

R Dambrauskienė

Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health SciencesKaunas, Lithuania
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Dambrauskienė, R
, 
R Gerbutavičius

R Gerbutavičius

Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health SciencesKaunas, Lithuania
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Gerbutavičius, R
, 
R Ugenskienė

R Ugenskienė

Lithuanian University of Health Sciences, Institute of Oncology, Oncology Research LaboratoryKaunas, Lithuania
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Ugenskienė, R
, 
R Jankauskaitė

R Jankauskaitė

Lithuanian University of Health Sciences, Institute of Oncology, Oncology Research LaboratoryKaunas, Lithuania
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Jankauskaitė, R
, 
A Savukaitytė

A Savukaitytė

Lithuanian University of Health Sciences, Institute of Oncology, Oncology Research LaboratoryKaunas, Lithuania
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Savukaitytė, A
, 
R Šimoliūnienė

R Šimoliūnienė

Department of Physics, Mathematics and Biophysics, Lithuanian University of Health SciencesKaunas, Lithuania
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Šimoliūnienė, R
, 
M Rudžianskienė

M Rudžianskienė

Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health SciencesKaunas, Lithuania
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Rudžianskienė, M
, 
R Gerbutavičienė

R Gerbutavičienė

Department of Drug Technology and Social Pharmacy, Faculty of Pharmacy, Lithuanian University of Health SciencesKaunas, Lithuania
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Gerbutavičienė, R
 oraz 
E Juozaitytė

E Juozaitytė

Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health SciencesKaunas, Lithuania
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Juozaitytė, E
  
Otwarty dostęp | 30 cze 2017
Molecular and immunohistochemical characteristics of complete hydatidiform moles
KB Kubelka-Sabit

KB Kubelka-Sabit

Department of Histopathology and Cytology, Clinical Hospital “Acibadem-Sistina”Skopje, Republic of Macedonia
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Kubelka-Sabit, KB
, 
I Prodanova

I Prodanova

Diagnostic Laboratory “Histolab”Skopje, Republic of Macedonia
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Prodanova, I
, 
D Jasar

D Jasar

Department of Histopathology and Cytology, Clinical Hospital “Acibadem-Sistina”Skopje, Republic of Macedonia
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Jasar, D
, 
G Bozinovski

G Bozinovski

Macedonian Academy of Sciences and Arts, Research Centre for Genetic Engineering and Biotechnology “Georgi D. Efremov”Skopje, Republic of Macedonia
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Bozinovski, G
, 
V Filipovski

V Filipovski

Department of Histopathology and Cytology, Clinical Hospital “Acibadem-Sistina”Skopje, Republic of Macedonia
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Filipovski, V
, 
S Drakulevski

S Drakulevski

Department of Histopathology and Cytology, Clinical Hospital “Acibadem-Sistina”Skopje, Republic of Macedonia
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Drakulevski, S
 oraz 
D Plaseska-Karanfilska

D Plaseska-Karanfilska

Macedonian Academy of Sciences and Arts, Research Centre for Genetic Engineering and Biotechnology “Georgi D. Efremov”Skopje, Republic of Macedonia
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Plaseska-Karanfilska, D
  
Otwarty dostęp | 30 cze 2017
Inherited thrombophilias could influence the reproductive outcome in women with systemic lupus erythematosus
R Robeva

R Robeva

Clinical Center of Endocrinology and Gerontology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Robeva, R
, 
D Tanev

D Tanev

Clinic of Rheumatology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Tanev, D
, 
S Andonova

S Andonova

National Genetic Laboratory, University Specialized Hospital for Active Treatment in Obstetrics and Gynecology, “Maichin dom”, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Andonova, S
, 
M Nikolova

M Nikolova

Clinic of Nephrology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Nikolova, M
, 
A Tomova

A Tomova

Clinical Center of Endocrinology and Gerontology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Tomova, A
, 
Ph Kumanov

Ph Kumanov

Clinical Center of Endocrinology and Gerontology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Kumanov, Ph
, 
A Savov

A Savov

National Genetic Laboratory, University Specialized Hospital for Active Treatment in Obstetrics and Gynecology, “Maichin dom”, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Savov, A
, 
R Rashkov

R Rashkov

Clinic of Rheumatology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Rashkov, R
 oraz 
Zl Kolarov

Zl Kolarov

Clinic of Rheumatology, Medical University, Sofia, Medical FacultySofia, Bulgaria
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Kolarov, Zl
  
Otwarty dostęp | 30 cze 2017
Genetic analyses of the NF1 gene in Turkish neurofibromatosis type I patients and definition of three novel variants
SD Ulusal

SD Ulusal

Department of Medical Genetics, Trakya University Faculty of MedicineEdirne, Turkey
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Ulusal, SD
, 
H Gürkan

H Gürkan

Department of Medical Genetics, Trakya University Faculty of MedicineEdirne, Turkey
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Gürkan, H
, 
E Atlı

E Atlı

Department of Medical Genetics, Trakya University Faculty of MedicineEdirne, Turkey
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Atlı, E
, 
SA Özal

SA Özal

Department of Opthalmology, Trakya University Faculty of MedicineEdirne, Turkey
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Özal, SA
, 
M Çiftdemir

M Çiftdemir

Department of Orthopedics and Traumatology, Trakya University Faculty of MedicineEdirne, Turkey
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Çiftdemir, M
, 
H Tozkır

H Tozkır

Department of Medical Genetics, Trakya University Faculty of MedicineEdirne, Turkey
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Tozkır, H
, 
Y Karal

Y Karal

Department of Pediatric Neurology, Trakya University Faculty of MedicineEdirne, Turkey
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Karal, Y
, 
H Güçlü

H Güçlü

Department of Opthalmology, Trakya University Faculty of MedicineEdirne, Turkey
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Güçlü, H
, 
D Eker

D Eker

Department of Medical Genetics, Trakya University Faculty of MedicineEdirne, Turkey
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Eker, D
 oraz 
I Görker

I Görker

Department of Child and Adolescent Psychiatry, Trakya University Faculty of MedicineEdirne, Turkey
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Görker, I
  
Otwarty dostęp | 30 cze 2017
Benign, pathogenic and copy number variations of unknown clinical significance in patients with congenital malformations and developmental delay
M Mihaylova

M Mihaylova

Department of Medical Genetics, Medical Faculty, Medical University of SofiaSofia, Bulgaria
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Mihaylova, M
, 
R Staneva

R Staneva

  • Department of Medical Genetics, Medical Faculty, Medical University of SofiaSofia, Bulgaria
  • Woman Health Hospital “Nadezhda”Sofia, Bulgaria
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Staneva, R
, 
D Toncheva

D Toncheva

Department of Medical Genetics, Medical Faculty, Medical University of SofiaSofia, Bulgaria
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Toncheva, D
, 
M Pancheva

M Pancheva

  • Department of Medical Genetics, Medical Faculty, Medical University of SofiaSofia, Bulgaria
  • Woman Health Hospital “Nadezhda”Sofia, Bulgaria
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Pancheva, M
 oraz 
S Hadjidekova

S Hadjidekova

  • Department of Medical Genetics, Medical Faculty, Medical University of SofiaSofia, Bulgaria
  • Woman Health Hospital “Nadezhda”Sofia, Bulgaria
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Hadjidekova, S
  

Case Report

Otwarty dostęp | 30 cze 2017
Sirenomelia associated with hypoplastic left heart in a newborn
H Turgut

H Turgut

Division of Neonatology, Department of Pediatrics, Inonu University School of MedicineMalatya, Turkey
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Turgut, H
, 
R Ozdemir

R Ozdemir

Division of Neonatology, Department of Pediatrics, Inonu University School of MedicineMalatya, Turkey
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Ozdemir, R
, 
IK Gokce

IK Gokce

Division of Neonatology, Department of Pediatrics, Inonu University School of MedicineMalatya, Turkey
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Gokce, IK
, 
C Karakurt

C Karakurt

Department of Pediatric Cardiology, Inonu University School of MedicineMalatya, Turkey
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Karakurt, C
 oraz 
A Karadag

A Karadag

Division of Neonatology, Department of Pediatrics, Inonu University School of MedicineMalatya, Turkey
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Karadag, A
  
Otwarty dostęp | 30 cze 2017
X-autosome and X-Y translocations in female carriers: X-chromosome inactivation easily detectable by 5-ethynyl-2-deoxyuridine (EdU)
M Donat

M Donat

Universtätsklinikum Jena, Institut für HumangenetikJena, Germany
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Donat, M
, 
A Louis

A Louis

Labor für Humangenetische DiagnostikHeidelberg, Germany
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Louis, A
, 
K Kreskowski

K Kreskowski

Universtätsklinikum Jena, Institut für HumangenetikJena, Germany
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Kreskowski, K
, 
M Ziegler

M Ziegler

Universtätsklinikum Jena, Institut für HumangenetikJena, Germany
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Ziegler, M
, 
A Weise

A Weise

Universtätsklinikum Jena, Institut für HumangenetikJena, Germany
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Weise, A
, 
I Schreyer

I Schreyer

  • Universtätsklinikum Jena, Institut für HumangenetikJena, Germany
  • Jena University Hospital, Center for Ambulant MedicineJena, Germany
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Schreyer, I
 oraz 
T Liehr

T Liehr

Universtätsklinikum Jena, Institut für HumangenetikJena, Germany
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Liehr, T
  

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