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Evolution of Genetic Techniques: Past, Present, and Beyond

BioMed research international, 2015-01, Vol.2015, p.461524-7

2015

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Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy

Journal of pediatric endocrinology & metabolism : JPEM, 2021-08, Vol.34 (8), p.1049

2021

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Laboratory Genetic Testing in Clinical Practice 2016

BioMed research international, 2017-01, Vol.2017, p.5798714-2

2017

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Laboratory Genetic Testing in Clinical Practice 2014

BioMed research international, 2015-01, Vol.2015, p.574798-1

2015

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A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow

Turkish journal of haematology, 2010-12, Vol.27 (4), p.299-302

2010

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Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing

BioMed research international, 2014-01, Vol.2014, p.210401-13

2014

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A 3’UTR Polymorphism of IL-6R Is Associated with Chinese Pediatric Tuberculosis

BioMed research international, 2014, Vol.2014, p.483759-7

2014

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Relationship between testicular sperm extraction results and AZF gene mutations

Türk üroloji dergisi, 2011-09, Vol.37 (3), p.229-234

2011

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VHL gene mutation in patients with renal tumors

Türk üroloji dergisi, 2011-09, Vol.37 (3), p.191-197

2011

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A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion

Journal of pediatric hematology/oncology, 2009-08, Vol.31 (8), p.592-594

2009

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Demonstration of Uniparental-Isodisomy on Chromosome 22q11.2 in a Patient With Childhood Schizophrenia and Facial Dysmorphology by Whole-Genome Analysis

The journal of neuropsychiatry and clinical neurosciences, 2012, Vol.24 (1), p.E13-E14

2012

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A novel Aspartoacylase (ASPA) Gene Mutation in Canavan Disease

Fetal and pediatric pathology, 2012-08, Vol.31 (4), p.236-239

2012

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Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven-Year Period

Journal of genetic counseling, 2011-06, Vol.20 (3), p.287-293

2011

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A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow

Turkish journal of haematology, 2010-12, Vol.27 (4), p.299-302

2010

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A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow / Kemik iliginde ekstra kromozom 5 ve X'e ilave Philadelphia kromozomu iceren akut lenfoblastik losemi olgusu

Turkish journal of haematology, 2010-12, Vol.27 (4), p.299

2010

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A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletion

Journal of pediatric hematology/oncology, 2009-08, Vol.31 (8), p.592-594

2009

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Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis

The Journal of neuropsychiatry and clinical neurosciences, 2012, Vol.24 (1), p.E13-E14

2012

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Congenital supratentorial cystic hemangioblastoma. Case report and review of the literature

Journal of neurosurgery, 2007-12, Vol.107 (6 Suppl), p.515-518

2007

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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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Evaluation of the SMN and NAIP genes in a family: homozygous deletion of the SMN2 gene in the fetus and outcome of the pregnancy

Genetic testing and molecular biomarkers, 2009-06, Vol.13 (3), p.287

2009

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Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome

Acta oncologica, 2008, Vol.47 (8), p.1604-1606

2008

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The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey

Genetic testing and molecular biomarkers, 2009-04, Vol.13 (2), p.163

2009

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Evolution of Genetic Techniques: Past, Present, and Beyond

Different clinical entities of the same mutation: a case report of three sisters with Wolfram syndrome and efficacy of dipeptidyl peptidase-4 inhibitor therapy

Laboratory Genetic Testing in Clinical Practice 2016

Laboratory Genetic Testing in Clinical Practice 2014

A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow

Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing

A 3’UTR Polymorphism of IL-6R Is Associated with Chinese Pediatric Tuberculosis

Relationship between testicular sperm extraction results and AZF gene mutations

VHL gene mutation in patients with renal tumors

A Severe α Thalassemia Case Compound Heterozygous for Hb Adana in α1 Gene and 20.5 kb Double Gene Deletion

Demonstration of Uniparental-Isodisomy on Chromosome 22q11.2 in a Patient With Childhood Schizophrenia and Facial Dysmorphology by Whole-Genome Analysis

A novel Aspartoacylase (ASPA) Gene Mutation in Canavan Disease

Reasons for Adult Referrals for Genetic Counseling at a Genetics Center in Izmir, Turkey: Analysis of 8965 Cases over an Eleven-Year Period

A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow

A case of acute lymphoblastic leukemia with additional chromosomes X and 5 associated with a Philadelphia chromosome in the bone marrow / Kemik iliginde ekstra kromozom 5 ve X'e ilave Philadelphia kromozomu iceren akut lenfoblastik losemi olgusu

A severe alpha thalassemia case compound heterozygous for Hb Adana in alpha1 gene and 20.5 kb double gene deletion

Demonstration of uniparental-isodisomy on chromosome 22q11.2 in a patient with childhood schizophrenia and facial dysmorphology by whole-genome analysis

Congenital supratentorial cystic hemangioblastoma. Case report and review of the literature

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

Evaluation of the SMN and NAIP genes in a family: homozygous deletion of the SMN2 gene in the fetus and outcome of the pregnancy

Chronic myelogenous leukemia exhibiting trisomy 14 due to a Robertsonian translocation with philadelphia chromosome

The evaluation of the referral reasons of patients at a tertiary pediatric genetic center in Izmir, Turkey

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