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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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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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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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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

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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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Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair

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

2012

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A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome

Genetic counseling, 2011, Vol.22 (1), p.11

2011

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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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A patient with 9q subtelomeric deletion syndrome with additional findings

Genetic counseling, 2012-01, Vol.23 (4), p.465

2012

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Thrombophilia gene mutations in oculoauriculovertebral spectrum

Genetic counseling, 2012, Vol.23 (1), p.65

2012

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A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutation

Genetic counseling, 2010-01, Vol.21 (2), p.225

2010

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Tumor suppressor gene alterations in patients with malignant mesothelioma due to environmental asbestos exposure in Turkey

Journal of carcinogenesis, 2006-08, Vol.5 (1), p.23-23

2006

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Prenatal and Postnatal Clinical Spectrum of a Mosaic Small Supernumerary Marker Chromosome 22

International Journal of Pediatrics and Child Health, 2019-03, Vol.7, p.36-39

2019

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Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion

Journal of Obstetrics and Gynaecology, 2019, Vol.39 (8), p.1175-1176

2019

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

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

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

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

Identification of an Alu-mediated 12.2-kb deletion of the complete LPAR6 (P2RY5) gene in a Turkish family with hypotrichosis and woolly hair

A Turkish patient with large 17p11.2 deletion presenting with Smith Magenis syndrome

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

A patient with 9q subtelomeric deletion syndrome with additional findings

Thrombophilia gene mutations in oculoauriculovertebral spectrum

A Turkish patient of typical Loeys-Dietz syndrome with a TGFBR2 mutation

Tumor suppressor gene alterations in patients with malignant mesothelioma due to environmental asbestos exposure in Turkey

Prenatal and Postnatal Clinical Spectrum of a Mosaic Small Supernumerary Marker Chromosome 22

Prenatal diagnosis of campomelic dysplasia due to SOX9 deletion

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