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1. Chromosomal breakage and sister chromatid exchange analysis in breast cancer patients with heterozygous BLM gene variants

8. Biyobankalar

12. Health Sciences Research: Nursing and Midwifery II

16. Determining T and B Cell development by TREC/KREC analysis in primary immunodeficiency patients and healthy controls

17. Bağlantı ve Tüm Ekzom Dizileme Analizlerinin Birlikte Değerlendirilmesiyle CIC Geninin İzole Distoni Adayı Olarak Belirlenmesi

18. HUKUKUN DİNAMİZMİ: YARGIDA REFORM

21. Otozomal Resesif Nörogelişimsel Bozukluğun Nedeni Olarak Bi-alelik NALCN Varyantı

31. İfade özgürlüğü bağlamında terör örgütünün propagandası suçu

32. ER, SOCS1, p15, E-cadherin and RARB are more Likely to be Members of the Methylator Phenotype of Adult and Childhood AML and Their Methylation is Primarly Regulated by an Overexpression of DNMT 3A

34. Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry

38. Aberrant methylation profile and microsatellit instability in Turkish sporadic colorectal carcinoma

39. Dealing with the gray zones in the management of gastric cancer: the consensus statement of the İstanbul Group

40. PTEN and AKT1 Variations in Childhood T-Cell Acute Lymphoblastic Leukemia.

42. Clinical phenotype of hereditary spastic paraplegia due to KIF1C gene mutations across life span

44. EVALUATION OF DISTANCE LEARNING STUDENTS PERFORMANCE USING FUZZY LOGIC

46. The Role of the Local Bone Marrow Renin-Angiotensin System in Multiple Myeloma.

49. Video yardımı ile minimal invazif 'port-akses' kalp cerrahisi erken dönem sonuçları

50. Aberrant Methylation Profile and Microsatellit Instability In Turkish Sporadic Colorectal Carcinoma.

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