Blog

Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A

Journal of Clinical Research in Pediatric Endocrinology, 2019By Ahmet Can Turkoglu February 20, 2019

Fatma Dursun, Gamze Özgürhan, Heves Kırmızıbekmez, Ece Keskin, and Bülent Hacıhamdioğlu

A biallelic mutation links MYORG to autosomal-recessive primary familial brain calcification

Brain - Journal of Neurology, 2019By Ahmet Can Turkoglu January 12, 2019

Yalda Forouhideh, Kathrin Müller, Wolfgang Ruf, Muhannad Assi, Tuncay Şeker et al.

Targeted Next-Generation Sequencing of MLH1, MSH2, and MSH6 Genes in Patients with Endometrial Carcinoma under 50 Years of Age

Balkan Medical Journal, 2019By Ahmet Can Turkoglu January 1, 2019

Taha Reşid Özdemir, Murat Alan, Muzaffer Sancı, and Altuğ Koç

A Turkish Female Twin Sister Patient with Fibular Aplasia, Congenital Tibia Pseudoarthrosis, Oligosyndactyly, and Negative WNT7A Gene Mutation

Journal of Pediatric Genetics, 2019By Ahmet Can Turkoglu November 18, 2018

Hale Önder Yılmaz, Duran Topak, Orkun Yılmaz, and Seda Çakmaklı

Association of E-selectin S128R polymorphism with hereditary breast carcinoma susceptibility in Turkish patients without BRCA1/2 germline mutations

Balkan Journal of Medical Genetics, 2018By Ahmet Can Turkoglu October 29, 2018

K Yararbas and PB Atalay

Comparison of two groups for the apolipoprotein E polymorphisms by using next generation sequencing: The first group with three consecutive abortions and the second group with at most one abortion in three consecutive pregnancies

Gene, 2018By Ahmet Can Turkoglu August 20, 2018

Evren Gumus

The Frequency of MEFV Gene Mutations and Genotypes in Sanliurfa Province, South-Eastern Region of Turkey, after the Syrian Civil War by Using Next Generation Sequencing and Report of a Novel Exon 4 Mutation (I423T)

Journal of Clinical Medicine, 2018By Ahmet Can Turkoglu May 7, 2018

Evren Gumus

Comorbidity of the congenital absence of the vas deferens

International Journal of Andrology, 2018By Ahmet Can Turkoglu February 27, 2018

E. C. Akinsal, N. Baydilli, M. E. Dogan and O. Ekmekcioglu

IKZF1 Deletions at Diagnose and Relapse of Childhood B-ALL

American Society of Hematology - Blood, 2017By Ahmet Can Turkoglu December 7, 2017

Yücel Erbilgin, Sinem Firtina, Ozden Hatirnaz, Tiraje Celkan, Zeynep Karakas et al.

A novel pathogenic frameshift variant of CD3E gene in two T-B+ NK+ SCID patients from Turkey

Immunogenetics, 2017By Ahmet Can Turkoglu June 9, 2017

Sinem Firtina, Yuk Yin, Ozden Hatirnaz, Serdar Nepesov, Osman Yesilbas et al.