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Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

Orphanet journal of rare diseases, 2011-06, Vol.6 (1), p.46-46

2011

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Effects of GLP-1 Receptor Polymorphisms on Adolescent Obesity

Acta medica Iranica, 2023, Vol.61 (4), p.238

2023

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Relationship between plasminogen activator inhibitor‐1 gene alterations and fibrosis in peritoneal dialysis patients

Therapeutic apheresis and dialysis, 2021-02, Vol.25 (1), p.97-102

2021

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The Generalization of Inflectional and Derivational Patterns to Novel Stems by L1 Turkish Learners of L2 English

Dilbilim araştırmaları, 2019-06, Vol.30 (1), p.103-121

2019

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Effects of APOE, ACE, PICALM, and CYP2D6 Gene Variants on Alzheimer's Disease

Current Psychiatry Research and Reviews, 2021-01, Vol.17 (2), p.127-136

2021

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The Investigation of English Teachers’ Views on Computer Assisted Language Learning

The Universal Academic Research Journal, 2020-01, Vol.2 (1), p.46-57

Ataman, Esra

2020

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Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy

Annals of the Indian Academy of Neurology, 2020-03, Vol.23 (2), p.206-210

2020

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Dilbilim Araştırmalarında Açık Bilim

Dilbilim araştırmaları, 2021-12, Vol.32 (2), p.149-175

2021

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Prenatally Diagnosed Turner Syndrome and Cystic Hygroma: Incidence and Reasons for Referrals

Fetal diagnosis and therapy, 2009-01, Vol.25 (1), p.58-61

2009

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Yetişkinlik Döneminde Dini Başa Çıkma Üzerine bir Araştırma

Ataman, Esra Burcu

2022

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Genetic Approach to Frequently Seen Pediatric Gastrointestinal System Diseases: Review

Turkiye Klinikleri Journal of Pediatrics, 2016, Vol.25 (3), p.159-173

2016

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Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype

International journal of cardiology, 2015-05, Vol.186, p.13-15

2015

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CYP4F22 gene mutations in patients with autosomal recessive congenital ichthyosis: Identification of two novel mutations

Turkish Journal of Dermatology, 2020, Vol.14 (4), p.90

2020

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A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel

Journal of Pediatric Endocrinology and Metabolism, 2016-09, Vol.29 (9), p.1111

2016

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The Multilingual Picture Database

Scientific data, 2022-07, Vol.9 (1), p.431-431, Article 431

2022

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The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

International journal of human genetics, 2015-01, Vol.60 (1), p.1-9

2015

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Identification of a novel frameshift heterozygous deletion in exon 8 of the PAX6 gene in a pedigree with aniridia

Molecular medicine reports, 2016-09, Vol.14 (3), p.2150-2154

2016

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Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

TURKISH JOURNAL OF MEDICAL SCIENCES, 2020-10, Vol.50 (6), p.1573-1579

2020

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Identification of the largest homozygous glycine decarboxylase gene deletion in a Turkish infant

Pediatrics and neonatology, 2018-12, Vol.59 (6), p.632-633

2018

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Phenotypic spectrum of CHARGE syndrome based on clinical characteristics

Turkish journal of medical sciences, 2018-10, Vol.48 (5), p.911-915

2018

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Thanatophoric Dysplasia Detected During Prenatal Period

Dokuz Eylül Üniversitesi Tıp Fakültesi dergisi, 2017, Vol.31 (3), p.181-186

2017

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The Processing of English-Turkish (False) Cognates: Evidence from a Backward Lexical Translation Task

Cankaya University Journal of Humanities and Social Sciences, 2021-12, Vol.15 (2), p.293-310

2021

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The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey

Genetic testing and molecular biomarkers, 2012-02, Vol.16 (2), p.150-153

2012

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Phenotypic variability of the kyphoscoliotic type of Ehlers-Danlos syndrome (EDS VIA): clinical, molecular and biochemical delineation

Effects of GLP-1 Receptor Polymorphisms on Adolescent Obesity

Relationship between plasminogen activator inhibitor‐1 gene alterations and fibrosis in peritoneal dialysis patients

The Generalization of Inflectional and Derivational Patterns to Novel Stems by L1 Turkish Learners of L2 English

Effects of APOE, ACE, PICALM, and CYP2D6 Gene Variants on Alzheimer's Disease

The Investigation of English Teachers’ Views on Computer Assisted Language Learning

Identification of PCDH19 gene mutations/deletions in patients with early onset epilepsy

Erratum: The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Dilbilim Araştırmalarında Açık Bilim

Prenatally Diagnosed Turner Syndrome and Cystic Hygroma: Incidence and Reasons for Referrals

Yetişkinlik Döneminde Dini Başa Çıkma Üzerine bir Araştırma

Genetic Approach to Frequently Seen Pediatric Gastrointestinal System Diseases: Review

Novel mutations in PTPN11 gene in two girls with Noonan syndrome phenotype

CYP4F22 gene mutations in patients with autosomal recessive congenital ichthyosis: Identification of two novel mutations

A novel splice site mutation of FGD1 gene in an Aarskog-Scott syndrome patient with a large anterior fontanel

The Multilingual Picture Database

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

Identification of a novel frameshift heterozygous deletion in exon 8 of the PAX6 gene in a pedigree with aniridia

Investigation of the most common clinical and imaging findings and the role of tubulin genes in the etiology of malformations of cortical development

Identification of the largest homozygous glycine decarboxylase gene deletion in a Turkish infant

Phenotypic spectrum of CHARGE syndrome based on clinical characteristics

Thanatophoric Dysplasia Detected During Prenatal Period

The Processing of English-Turkish (False) Cognates: Evidence from a Backward Lexical Translation Task

The phenotypic and molecular genetic spectrum of Alström syndrome in 44 Turkish kindreds and a literature review of Alström syndrome in Turkey

The rate of sex chromosome aneuploidies in prenatal diagnosis and subsequent decisions in Western Turkey

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