Investigation of Genes Associated With Atherosclerosis in Patients With Systemic Lupus Erythematosus

por BALCI, Mehmet Ali, ATLI, Engin, GüRKAN, Hakan
Publicado 2021

Two Cases of Cystic Fibrosis with Compound Heterozygous Variants Reported for the First Time

por Yalçıntepe, Sinem, Gürkan, Hakan, Atlı, Engin, Sayın, Niyazi Cenk, Başaran, Ümit Nusret
Publicado 2020

Two Novel Pathogenic FBN1 Variations and Their Phenotypic Relationship of Marfan Syndrome

por Yalcintepe, Sinem, Demir, Selma, Atli, Emine Ikbal, Deveci, Murat, Atli, Engin, Gurkan, Hakan
Publicado 2020

Investigating the Genetic Etiology of Pediatric Patients with Peripheral Hypotonia Using the Next-Generation Sequencing Method

por Eker, Damla, Gurkan, Hakan, Karal, Yasemin, Yalcintepe, Sinem, Demir, Selma, Atli, Engin, Karasalihoglu, Serap T.
Publicado 2022

Investigation of the Genetic Etiology in Idiopathic Generalized Epileptic Disorders by Targeted Next-generation Sequencing Technique

por Atlı, Engin, Gürkan, Hakan, Güldiken, Babürhan, Eker, Damla, Yalçıntepe, Sinem, Demir, Selma, Atlı, Emine İkbal
Publicado 2023

Clinical Features of Aberrations Chromosome 22q: A Pilot Study

por Atli, Emine Ikbal, Atli, Engin, Yalcintepe, Sinem, Demir, Selma, Mail, Cisem, Eker, Damla, Ozen, Yasemin, Gurkan, Hakan
Publicado 2021

Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period

por Atli, Emine Ikbal, Atli, Engin, Yalcintepe, Sinem, Demir, Selma, Kalkan, Rasime, Akurut, Cisem, Ozen, Yasemin, Gurkan, Hakan
Publicado 2021

Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants

por Demir, Selma, Yalçıntepe, Sinem, Atlı, Engin, Yalçın, Yelda, İkbal Atlı, Emine, Eker, Damla, Karal, Yasemin, Gürkan, Hakan
Publicado 2021

Investigation on the Effects of Modifying Genes on the Spinal Muscular Atrophy Phenotype

por Zhuri, Drenushe, Gurkan, Hakan, Eker, Damla, Karal, Yasemin, Yalcintepe, Sinem, Atli, Engin, Demir, Selma, Atli, Emine Ikbal
Publicado 2022

The Application of Next Generation Sequencing Maturity Onset Diabetes of the Young Gene Panel in Turkish Patients from Trakya Region

por Yalçıntepe, Sinem, Özgüç Çömlek, Fatma, Gürkan, Hakan, Demir, Selma, Atlı, Emine İkbal, Atlı, Engin, Eker, Damla, Tütüncüler Kökenli, Filiz
Publicado 2021

The Frequency of SMN1, SMN2 Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method

por Yalcintepe, Sinem, Karal, Yasemin, Demir, Selma, Atli, Emine Ikbal, Atli, Engin, Eker, Damla, Mail, Cisem, Zhuri, Drenushe, Guler, Hazal Sezginer, Gurkan, Hakan
Publicado 2023

The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies

por Atli, Emine Ikbal, Gurkan, Hakan, Atli, Engin, Kirkizlar, Hakki Onur, Yalcintepe, Sinem, Demir, Selma, Demirci, Ufuk, Eker, Damla, Mail, Cisem, Kalkan, Rasime, Demir, Ahmet Muzaffer
Publicado 2021

Germline Pathogenic Variants Identified by Targeted Next-Generation Sequencing of Susceptibility Genes in Pheochromocytoma and Paraganglioma

por Yalcintepe, Sinem, Gurkan, Hakan, Korkmaz, Fatma Nur, Demir, Selma, Atli, Engin, Eker, Damla, Guler, Hazal Sezginer, Zhuri, Drenusha, Atli, Emine Ikbal, Salt, Semra Ayturk, Sahin, Mustafa, Guldiken, Sibel
Publicado 2021

Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes

por YALÇINTEPE, Sinem, GÖRKER, Işık, DEMİR, Selma, ATLI, Emine İkbal, ATLI, Engin, TOZKIR, Hilmi, SÜT, Necdet, ÖZEN, Yasemin, EKER, Damla, MAİL, Çisem, GÜLER, Hazal SEZGİNER, ZHURI, Drenushe, GURKAN, Hakan
Publicado 2021