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Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations

Genetic testing and molecular biomarkers, 2012-04, Vol.16 (4), p.279-286

2012

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Re-evaluation of Genetic Variants in Parkinson’s Disease Using Targeted Panel and Next-Generation Sequencing

Twin research and human genetics, 2023-04, Vol.26 (2), p.164-170

2023

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Combined germline variations of thrombophilic genes promote genesis of lung cancer

Asian Pacific journal of cancer prevention : APJCP, 2013-01, Vol.14 (9), p.5449-5454

2013

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The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients

Clinical neurology and neurosurgery, 2021-03, Vol.202, p.106487-106487, Article 106487

2021

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Prevelance of common YMDD motif mutations in long term treated chronic HBV infections in a Turkish population

Asian Pacific journal of cancer prevention : APJCP, 2013-01, Vol.14 (9), p.5489-5494

2013

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Design of a new balun bandpass filter with single‐band balance and dual‐band filtering characteristics

Microwave and optical technology letters, 2019-11, Vol.61 (11), p.2586-2590

2019

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Maximum lift/drag ratio improvement of TUAVs via small aerodynamic modifications

Aircraft engineering and aerospace technology, 2018-11, Vol.90 (9), p.1438-1444

2018

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An alternative coupling matrix arrangement for capacitively loaded multi-mode microstrip diplexers having close channel bands

International journal of electronics and communications, 2023-03, Vol.161, p.154540, Article 154540

2023

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Blau syndrome with a rare mutation in exon 9 of NOD2 gene

Autoimmunity (Chur, Switzerland), 2019-11, Vol.52 (7-8), p.256-263

2019

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Epigenetic Inactivation of Tumor Suppressor SFRP2 and Point Mutation in KRAS Proto-Oncogene in Fistula - Associated Mucinous Type Anal Adenocarcinoma: Report of Two Cases

Internal Medicine, 2010, Vol.49(15), pp.1637-1640

2010

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The role of apoptosis and protective effect of carnitine in contralateral testicular injury in experimental unilateral testicular torsion

Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES, 2009-11, Vol.15 (6), p.529

2009

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Aerodynamic Optimization of a UAV Wing subject to Weight, Geometric, Root Bending Moment, and Performance Constraints

International Journal of Aerospace Engineering, 2019, Vol.2019 (2019), p.1-14

2019

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The diagnostic accuracy of non-invasive fetal RhD genotyping by using cell-free fetal DNA in maternal plasma

Family practice and palliative care (Online), 2019-03, Vol.4 (1), p.1-6

2019

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Design of fourth order microstrip filter using the open loop resonator with a novel interdigital loading element

2017 IEEE MTT-S International Microwave Symposium (IMS), 2017, p.1819-1822

2017

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A novel microstrip diplexer design with tunable bandwidths and switchable channels for 4.5G applications

Elektrik : Turkish journal of electrical engineering & computer sciences, 2017, Vol.25, p.4445-4456

2017

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Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G variations in breast carcinoma

Asian Pacific journal of cancer prevention : APJCP, 2013-01, Vol.14 (5), p.2903-2908

2013

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The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

The Egyptian journal of medical human genetics, 2018-10, Vol.19 (4), p.437-441

2018

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Copy number variations in patients with idiopathic recurrent pregnancy loss: an array-CGH approach

Turkish journal of medical sciences, 2022-01, Vol.52 (5), p.1689-1696

2022

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Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

Annals of Saudi medicine, 2014-07, Vol.34 (4), p.340-345

2014

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A Frame-Shift Mutation in the SLC34A2 Gene in Three Patients with Pulmonary Alveolar Microlithiasis in an Inbred Family

Internal Medicine, 2010, Vol.49(1), pp.45-49

2010

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Alterations in promoter methylation status of tumor suppressor HIC1, SFRP2, and DAPK1 genes in prostate carcinomas

DNA and cell biology, 2012-05, Vol.31 (5), p.826-832

2012

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Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

Biodiscovery, 2017-08, Vol.20, p.e20113-2

2017

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Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation

Family practice and palliative care (Online), 2018-04, Vol.3 (1), p.23-27

2018

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A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels

Hemoglobin, 2022-03, Vol.46 (2), p.87-90

2022

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A New Mutation, Hb A 2 -Canakkale [δ10(A7)Ala→Val; HBD : c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A 2 Levels

Hemoglobin, 2022-03, Vol.46 (2), p.87-90

2022

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Recurrent pregnancy loss and its relation to combined parental thrombophilic gene mutations

Re-evaluation of Genetic Variants in Parkinson’s Disease Using Targeted Panel and Next-Generation Sequencing

Combined germline variations of thrombophilic genes promote genesis of lung cancer

The high frequency of chromosomal copy number variations and candidate genes in epilepsy patients

Prevelance of common YMDD motif mutations in long term treated chronic HBV infections in a Turkish population

Design of a new balun bandpass filter with single‐band balance and dual‐band filtering characteristics

Maximum lift/drag ratio improvement of TUAVs via small aerodynamic modifications

An alternative coupling matrix arrangement for capacitively loaded multi-mode microstrip diplexers having close channel bands

Blau syndrome with a rare mutation in exon 9 of NOD2 gene

Epigenetic Inactivation of Tumor Suppressor SFRP2 and Point Mutation in KRAS Proto-Oncogene in Fistula - Associated Mucinous Type Anal Adenocarcinoma: Report of Two Cases

The role of apoptosis and protective effect of carnitine in contralateral testicular injury in experimental unilateral testicular torsion

Aerodynamic Optimization of a UAV Wing subject to Weight, Geometric, Root Bending Moment, and Performance Constraints

The diagnostic accuracy of non-invasive fetal RhD genotyping by using cell-free fetal DNA in maternal plasma

Design of fourth order microstrip filter using the open loop resonator with a novel interdigital loading element

A novel microstrip diplexer design with tunable bandwidths and switchable channels for 4.5G applications

Germ-line MTHFR C677T, FV H1299R and PAI-1 5G/4G variations in breast carcinoma

The clinical, cytogenetics and molecular characterization of inverted duplication/deletion of chromosome 8p in a boy with mental and motor retardation: Genotype-phenotype correlation in a case report

Copy number variations in patients with idiopathic recurrent pregnancy loss: an array-CGH approach

Association of endothelial nitric oxide synthase Glu298Asp gene polymorphism in psoriasis cases with hypertension

A Frame-Shift Mutation in the SLC34A2 Gene in Three Patients with Pulmonary Alveolar Microlithiasis in an Inbred Family

Alterations in promoter methylation status of tumor suppressor HIC1, SFRP2, and DAPK1 genes in prostate carcinomas

Two candidate genes for recurrent pregnancy loss and infertility: Could ZP3 and UPK3B give us new diagnostic and therapeutic approach?

Macular and choroidal thickness of children with Familial Mediterranean Fever gene mutation

A New Mutation, Hb A2-Canakkale [δ10(A7)Ala→Val; HBD: c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A2 Levels

A New Mutation, Hb A 2 -Canakkale [δ10(A7)Ala→Val; HBD : c.32C>T], and Other Well-Known δ Variants Identified in a Selected Cohort with Low Hb A 2 Levels

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