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A Negative Correlation Between MEFV Mutations and Allergic Diseases

The journal of pediatric research, 2022-06, Vol.9 (2), p.132-137

2022

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GATA-4 Variants in Two Unrelated Cases with 46, XY Disorder of Sex Development and Review of the Literature

Journal of clinical research in pediatric endocrinology, 2022-12, Vol.14 (4), p.469-474

2022

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CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis

Internal Medicine, 2011, Vol.50(21), pp.2457-2461

2011

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Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

Annals of Saudi medicine, 2019-11, Vol.39 (6), p.382-387

2019

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The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

The journal of international advanced otology, 2019-12, Vol.15 (3), p.373-378

2019

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An Examination of Paraoxonase 1 Gene Polymorphism in Cases of Chronic Otitis Media

ENT Updates, 2020-04

2020

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Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population

Turkish journal of nephrology, 2020-10, Vol.29 (4), p.304-309

2020

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The Association of MCP-1 Level and MCP-1 -2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension

Gazi tıp dergisi, 2021-01, Vol.32 (1), p.28-32

2021

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Angiotensin-Converting Enzyme (ACE) I/D and Alpha-Adducin (ADD1) G460W Gene Polymorphisms in Turkish Patients with Severe Chronic Tinnitus

The journal of international advanced otology, 2016-04, Vol.12 (1), p.77-81

2016

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Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

Molecular cytogenetics, 2015-11, Vol.8 (92), p.92, Article 92

2015

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The Association of Plasminogen Activator Inhibitor Type 1 (PAI-1) Level and PAI-1 4G/5G Gene Polymorphism with the Formation and the Grade of Endometrial Cancer

Biochemical genetics, 2017-08, Vol.55 (4), p.314-321

2017

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Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease

Cornea, 2019-03, Vol.38 (3), p.379

2019

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Heterozygous Deletion of Exon 8 in WFS1 Gene in Two Wolfram Syndrome Probands with Hearing Loss: Case Report

Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi, 2011, Vol.31 (1), p.245-250

2011

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Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Which a Different De Novo Actg2 Gene Mutation was Detected: A Case Report

Fetal and pediatric pathology, 2018-03, Vol.37 (2), p.109-116

2018

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The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study

Journal of gynecology obstetrics and human reproduction, 2019-09, Vol.48 (7), p.521-525

2019

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Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of Turkey

Biochemical genetics, 2016-08, Vol.54 (4), p.448-456

2016

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8Q22.3-Q24.23 Duplication: A Case Report

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (2), p.1

2017

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Bcıı-RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Renal failure, 2015-03, Vol.37 (2), p.292-296

2015

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Bc -RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Renal failure, 2015-03, Vol.37 (2), p.292-296

2015

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Bcı ı —RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Renal failure, 2015-02, Vol.37 (2), p.292-296

2015

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Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers

Molecular biology reports, 2011-06, Vol.38 (5), p.3195-3200

2011

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A Balanced Robertsonian Translocation (13;14) of a Male: A Case Report

Journal of medical cases, 2014, Vol.5 (12), p.615-617

2014

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8Q22.3-Q24.23 Duplication: A Case Report

Journal of clinical research in pediatric endocrinology, 2017-06, Vol.9 (1), p.1

2017

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Heterozygous Deletion of Exon 8 in WFS1 Gene in TwoWolfram Syndrome Probands with Hearing Loss: Case Report/Isitme Kaybi Olan Wolfram Sendromlu Iki Olguda WFS1 Geni Ekson 8'de Heterozigot Delesyon

Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi, 2011-01, Vol.31 (1), p.245

2011

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Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

Molecular cytogenetics, 2015, Vol.8, p.92-92

2015

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A Negative Correlation Between MEFV Mutations and Allergic Diseases

GATA-4 Variants in Two Unrelated Cases with 46, XY Disorder of Sex Development and Review of the Literature

CCR2 Polymorphism in Chronic Renal Failure Patients Requiring Long-Term Hemodialysis

Prevalence of MEFV gene mutations in a large cohort of patients with suspected familial Mediterranean fever in Central Anatolia

The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

An Examination of Paraoxonase 1 Gene Polymorphism in Cases of Chronic Otitis Media

Analysis of PKD1 and PKD2 Gene Mutations for Autosomal Dominant Polycystic Kidney Disease Cases in Turkish Population

The Association of MCP-1 Level and MCP-1 -2518 A/G and CCR2 190 G/A Gene Polymorphisms with COPD and Pulmonary Hypertension

Angiotensin-Converting Enzyme (ACE) I/D and Alpha-Adducin (ADD1) G460W Gene Polymorphisms in Turkish Patients with Severe Chronic Tinnitus

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

The Association of Plasminogen Activator Inhibitor Type 1 (PAI-1) Level and PAI-1 4G/5G Gene Polymorphism with the Formation and the Grade of Endometrial Cancer

Ocular and Genetic Characteristics Observed in Two Cases of Fish-Eye Disease

Heterozygous Deletion of Exon 8 in WFS1 Gene in Two Wolfram Syndrome Probands with Hearing Loss: Case Report

Megacystis Microcolon Intestinal Hypoperistalsis Syndrome in Which a Different De Novo Actg2 Gene Mutation was Detected: A Case Report

The type and prevalence of chromosomal abnormalities in couples with recurrent first trimester abortions: A Turkish retrospective study

Prevalence of Fabry Disease in Familial Mediterranean Fever Patients from Central Anatolia of Turkey

8Q22.3-Q24.23 Duplication: A Case Report

Bcıı-RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Bc -RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Bcı ı —RFLP profiles for serum amiloid A1 and mutated MEFV gene prevalence in chronic renal failure patients requiring long-term hemodialysis

Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers

A Balanced Robertsonian Translocation (13;14) of a Male: A Case Report

8Q22.3-Q24.23 Duplication: A Case Report

Heterozygous Deletion of Exon 8 in WFS1 Gene in TwoWolfram Syndrome Probands with Hearing Loss: Case Report/Isitme Kaybi Olan Wolfram Sendromlu Iki Olguda WFS1 Geni Ekson 8'de Heterozigot Delesyon

Recombinant chromosome with partial 14 q trisomy due to maternal pericentric inversion

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