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Frequency of Genetic Mutations Associated with Thromboembolism in the Western Black Sea Region

Internal Medicine, 2011, Vol.50(1), pp.17-21

2011

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Unique variant of Adams–Oliver syndrome with dilated cardiomyopathy and heart block

Pediatrics international, 2013-08, Vol.55 (4), p.508-512

2013

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Expression of the syncytin-1 and syncytin-2 genes in the trophoblastic tissue of the early pregnancy losses with normal and abnormal karyotypes

Gene, 2020-05, Vol.741, p.144533-144533, Article 144533

2020

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The value of interleukin‐12B (p40) gene promoter polymorphism in patients with schizophrenia in a region of East Turkey

Psychiatry and clinical neurosciences, 2008-06, Vol.62 (3), p.307-312

2008

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Investigation of the Relationship Between IL28B Polymorphisms and Plasma IL28B Levels in Patients with Chronic Hepatitis B or C

Mikrobiyoloji bülteni, 2021-07, Vol.55 (3), p.374-388

2021

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Relationship between Primary Nodal Generalized Osteoarthritis with Tissue Antigens HLA-A and HLA-B in the Western Black Sea Region of Turkey

Internal Medicine, 2011, Vol.50(6), pp.545-550

2011

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Direct embryonic biopsy with transcervical embryoscopy is an effective method for karyotyping and morphology assessment in miscarriages

Journal of assisted reproduction and genetics, 2024-07, Vol.41 (7), p.1925-1931

2024

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The interrelation between the high expression level of MIR34a and the trisomic abortion materials

The journal of obstetrics and gynaecology research, 2024-05, Vol.50 (5), p.842-848

2024

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Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses

The journal of maternal-fetal & neonatal medicine, 2017-07, Vol.30 (13), p.1579-1583

2017

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Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion

Journal of obstetrics and gynaecology, 2019-11, Vol.39 (8), p.1175-1176

2019

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The relationship between the clinical course of SARS-CoV-2 infections and ACE2 and TMPRSS2 expression and polymorphisms

Advances in clinical and experimental medicine : official organ Wroclaw Medical University, 2024-01, Vol.33 (1), p.39-51

2024

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Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region

Turkish journal of pediatrics, 2018-01, Vol.60 (1), p.94-98

2018

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Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case

American journal of medical genetics. Part A, 2014-07, Vol.164A (7), p.1770-1776

2014

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Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing

Turkish journal of medical sciences, 2018-04, Vol.48 (2), p.386-390

2018

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The relation between isolated micropenis in childhood with CAG and GGN repeat polymorphisms in the androgen receptor gene

Turkish journal of medical sciences, 2018-04, Vol.48 (2), p.430-434

2018

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Klinefelter Sendromlu ve normal karyotipli non-obstruktif azospermik hastaların in vitro fertilizasyon sonuçlarının değerlendirilmesi

Gazi tıp dergisi, 2020-09, Vol.31 (4), p.583-586

2020

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Retrospective analysis of the association of the expression and single nucleotide polymorphisms (SNPs) of the TLR4, PTX3 and Dectin‐1 (CLEC/A) genes with development of invasive aspergillosis among haematopoietic stem cell transplant recipients with oncohaematological disorders

Mycoses, 2020-08, Vol.63 (8), p.832-839

2020

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A Turkish family with Nance-Horan syndrome due to a novel mutation

Gene, 2013-08, Vol.525 (1), p.141-145

2013

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Interleukin-10 gene promoter polymorphism in patients with schizophrenia in a region of East Turkey

The world journal of biological psychiatry, 2009, Vol.10 (4_2), p.461-468

2009

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Cochlear involvement in Familial Mediterranean Fever: A new feature of an old disease

International journal of pediatric otorhinolaryngology, 2012-02, Vol.76 (2), p.244-247

2012

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Spondyloepiphyseal dysplasia tarda with progressive arthropathy with delayed diagnosis

Turkish journal of medical sciences, 2008-02, Vol.38 (1), p.83-89

2008

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Unique variant of A dams– O liver syndrome with dilated cardiomyopathy and heart block

Pediatrics international, 2013-08, Vol.55 (4), p.508-512

2013

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The effect of octreotide, an analog of somatostatin, on bleomycin-induced interstitial pulmonary fibrosis in rats

Drug and chemical toxicology (New York, N.Y. 1978), 2013-04, Vol.36 (2), p.181-186

2013

Volltextzugriff (PDF)

Identification of an A lu‐mediated 12.2‐kb deletion of the complete LPAR 6 ( P2 RY 5 ) gene in a T urkish family with hypotrichosis and woolly hair

Experimental dermatology, 2012-06, Vol.21 (6), p.469-471

2012

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Cystic hygroma: a single-centre experience

Singapore medical journal, 2023-04

2023

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Frequency of Genetic Mutations Associated with Thromboembolism in the Western Black Sea Region

Unique variant of Adams–Oliver syndrome with dilated cardiomyopathy and heart block

Expression of the syncytin-1 and syncytin-2 genes in the trophoblastic tissue of the early pregnancy losses with normal and abnormal karyotypes

The value of interleukin‐12B (p40) gene promoter polymorphism in patients with schizophrenia in a region of East Turkey

Investigation of the Relationship Between IL28B Polymorphisms and Plasma IL28B Levels in Patients with Chronic Hepatitis B or C

Relationship between Primary Nodal Generalized Osteoarthritis with Tissue Antigens HLA-A and HLA-B in the Western Black Sea Region of Turkey

Direct embryonic biopsy with transcervical embryoscopy is an effective method for karyotyping and morphology assessment in miscarriages

The interrelation between the high expression level of MIR34a and the trisomic abortion materials

Confirmation of the prenatal mosaic trisomy 2 via fetal USG and cytogenetic analyses

Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion

The relationship between the clinical course of SARS-CoV-2 infections and ACE2 and TMPRSS2 expression and polymorphisms

Clinical findings in cases with 9q deletion encompassing the 9q21.11q21.32 region

Chromosomal-array analysis reveals partial 11q duplication and partial 12p deletion in a mildly affected case

Microdeletion and mutation analysis of the SHOX gene in patients with idiopathic short stature with FISH and sequencing

The relation between isolated micropenis in childhood with CAG and GGN repeat polymorphisms in the androgen receptor gene

Klinefelter Sendromlu ve normal karyotipli non-obstruktif azospermik hastaların in vitro fertilizasyon sonuçlarının değerlendirilmesi

Retrospective analysis of the association of the expression and single nucleotide polymorphisms (SNPs) of the TLR4, PTX3 and Dectin‐1 (CLEC/A) genes with development of invasive aspergillosis among haematopoietic stem cell transplant recipients with oncohaematological disorders

A Turkish family with Nance-Horan syndrome due to a novel mutation

Interleukin-10 gene promoter polymorphism in patients with schizophrenia in a region of East Turkey

Cochlear involvement in Familial Mediterranean Fever: A new feature of an old disease

Spondyloepiphyseal dysplasia tarda with progressive arthropathy with delayed diagnosis

Unique variant of A dams– O liver syndrome with dilated cardiomyopathy and heart block

The effect of octreotide, an analog of somatostatin, on bleomycin-induced interstitial pulmonary fibrosis in rats

Identification of an A lu‐mediated 12.2‐kb deletion of the complete LPAR 6 ( P2 RY 5 ) gene in a T urkish family with hypotrichosis and woolly hair

Cystic hygroma: a single-centre experience

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