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Yayın Arama

Toplam 27822 kayıt

Intercellular Adhesion Molecule 1 K469E and Angiotensinogen T207M Polymorphisms in Coronary Slow Flow
0 0
2014 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
MEDICAL PRINCIPLES AND PRACTICE

Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population
0 0
2009 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Biologia

Clinical and molecular analysis of common MEFV gene mutations in familial Mediterranean fever in Sivas population
0 0
2009 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Biologia

Combined point mutations in codon 12 and 13 of KRAS oncogene in prostate carcinomas
0 0
2012 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Mol Biol Rep

Increased T Allele Frequency of 677 C T Polymorphism in the Methylenetetrahydrofolate Reductase Gene in Differentiated Thyroid Carcinoma
0 0
2012 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Genet Test Mol Biomarkers

Scientific Research
0 0
2010 Özgün Makale SCI/SSCI/AHCI ESCI Scopus
Health

Maternal Fetal eNOS Genotipleri ile Spontan Abortus İlişkisi
0 0
2013 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Erişkin Yaşta Görülen Genetik Hastalıklar Sempozyumu

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress. 17-20 April 2019

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress. 17-20 April 2019, Edirne/Turkey.

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress. 17-20 April 2019, Edirne/Turkey.

Mosaic Trisomy 9 Presenting With Congenital Diaphragmatic Hernia And Facial Dysmorphism
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balcan Human Genetic Congress. 17-20 April 2019, Edirne/Turkey.

BCL11B gene may be a candidate gene for mastocytosis in a patient with partial trisomy of distal 14q
0 0
2019 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
13th Balkan Congress of Human Genetics

Rare disease or rare diagnosed diseases: Blau syndrome with a rare mutation in exon 9 of NOD2 gene from Canakkale
0 0
2018 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
European Biotechnology Congress

The RFLP profiles at BRAF V600E mutations in thyroid FNAB nodules
0 0
2015 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
Europan Biotechnology Congress

Kronik hepatit B tedavisi alan hastalarda yaygın rtL80V I ve rtM204V I YMDD mutasyon profilleri
0 0
2009 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
11. Ulusal Tıbbi Biyoloji ve Genetik Kongresi

3 Metilkolantren Uygulanan Ratlarda Oluşan Yumuşak Doku Tümörlerinde Ki ras Ekson 2 Geni Mutasyon Analizi
0 0
2004 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
II.Klinik Biyokimya ve Kanser Sempozyumu

Down sendromlu bebek sahibi eşlerde anafaz köprüsü
0 0
0 Tebliğ/Bildiri SCI/SSCI/AHCI ESCI Scopus
XII. Gevher Nesibe Tıp Günleri, Türk Dünyası Tıp Bilimleri Kongresi