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26 results on '"TEKİN, Mustafa"'

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1. Wear behavior of in-situ oxide dispersion strengthened Fe-8Ni alloy with Zr additions

2. OG-AG ELEKTRİK ŞEBEKELERİNDE DİNAMİK KONTROLLÜ KOMPANZASYON UYGULAMASI

3. VARS1 Mutations Associated with Neurodevelopmental Disorder Are Located on A Short Amino Acid Stretch of The Anticodon-Binding Domain

4. Do we really ponder about necessity of intravenous hydration in acute bronchiolitis?

5. Topical Steroid Induced Latrogenic Adrenocortical Insufficiency

6. Opinions of the Parents of Children with Upper Respiratory Tract Infection about the Influenza Vaccine

7. Frequency Of Rotavirus in Children With Acute Gastroenteritis

8. Complete Heart Block Related to Mumps Myocarditis in an 80-Year-Old Woman

9. Additional file 1: Figure S1. of Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome

10. Additional file 1: Figure S1. of Novel MASP1 mutations are associated with an expanded phenotype in 3MC1 syndrome

11. Trakeobronchial toy bow in a seven years old child: Case report

12. Audiological Findings In Otospondylomegaepiphyseal Dysplasia (Osmed) Associated With A Novel Mutation In Col11A2

13. Antenna Control With Pi, Lqg And H∞ Controllers

14. A Complex Tfap2A Allele Is Associated With Branchio-Oculo-Facial Syndrome And Inner Ear Malformation In A Deaf Child

15. Mawlana in Distinction Between Aristocratic Islam and Folk Islam

16. RELIGION IN THE CONTEXT OF SOCIAL INTEGRATION AND SOCIAL DISINTEGRATION IN MAWLANA JALAL AL-DIN RUMI’S WORKS

17. BIBLIOGRAPHY ON MAWLANA

18. TÜRKİYE’DE AYDIN KADINLARIN DİN ANLAYIŞI

20. The Fukuyama Type Congenital Muscular Dystrophy with hyperekplexia

21. A Novel Genetic Basis For Systemic Vasculitis: Polyarteritis Nodosa Caused By Recessive Mutations In An Immune-Related Gene

22. Humerus cisim kırıklarında minimal invaziv perkütan plak osteosentezi (MIPPO)

23. Detection of Ibuprofen Levels by High Performance Liquid Chromatography After Phonophoresis in the Tissues of Patients with Knee Osteoarthritis: A Controlled Preliminary Study

24. Novel EYA1 variants causing Branchio-oto-renal syndrome

25. Nijmegen-Breakage Syndrome; Two Siblings Presenting with Different Phenotypes

26. Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability

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