Determining of cytogenetic differences and number of FMR 1 gene trinucleotide repeats in children with Fragile X syndrome prediagnosis
2010
0 görüntülenme
0 i̇ndirme
Danışman: Prof. Dr. Osman Demirhan
Özet (EN)
In this study, our goal was to determine the syndrome ratio of children who attended to our clinic with FXS pre-diagnosis using both cytogenetic and molecular analysis methods.
Yazar
Dr. Onur Özer
Bu Yayına Nasıl Atıf Yapılır
Onur Özer (Master Thesis). Determining of cytogenetic differences and number of FMR 1 gene trinucleotide repeats in children with Fragile X syndrome prediagnosis, 2010, Çukurova University.
Anahtar Kelimeler
Lisans
Tüm Hakları Saklıdır
Bu eser belirtilen lisans koşulları altında paylaşılmaktadır.
Çukurova University tezlerinden daha fazlası
- The effects of collaborative video-blog projects on Turkish EFL students' linguistic and digital literacy skills(2025)
- Role of Anti-Mullerian Hormone (AMH) in ındicating the over reserve of IVF Patients(2011)
- Credit risk management in banking sector: An application of variables determining credit risk in Turkish banking sector(2011)
- Comparasion of the shear bond strength of two different precoated and uncoated ceramic brackets(2014)
- The control tests of four anode photomultiplier tubes for hf calorimeter of CMS detector(2014)
- The predictive strength of career decision making difficulties on high school students' career maturity accordi̇ng to their levels of focus of control(2017)