619 results on '"Boduroğlu A"'
Search Results
2. A spectrum of TP63-related disorders with eight affected individuals in five unrelated families
3. International Academic Research & Reviews in Education Sciences -II-
4. Spondylo-meta-epiphyseal dysplasia (SMED), short limb-hand abnormal calcification type: Further expanding the mutational spectrum and dental findings of three new patients
5. Mean-Reverting Portfolio Optimization via a Surrogate Risk Measure - Conditional Desirability Value at Risk
6. A Life-Threatening Complication in a Patient with Ehlers-Danlos Syndrome Musculocontractural Type
7. A lethal and rare cause of arthrogryposis: Glyt1 encephalopathy
8. 6. Sınıf Türkçe Ortak Sınavının Cinsiyete ve Okul Coğrafyasına Göre Ölçme Değişmezliğinin İncelenmesi: Niğde İli Örneği.
9. Investigation of the relationship between comprehensive echocardiograhic findings and CRP/prealbumin ratio in patients with metabolic syndrome.
10. Professional, educational and psychosocial impacts of the COVID-19 pandemic on pediatricians.
11. Hyaline fibromatosis syndrome: a rare, yet recognizable syndrome
12. Sleep disordered breathing in patients with Prader willi syndrome: Impact of underlying genetic mechanism
13. Mean-Reverting Portfolio Optimization via a Surrogate Risk Measure - Conditional Desirability Value at Risk
14. Relationship Between Hemoglobin Glycation and AHI Index in Patients With Non-diabetic OSAS
15. Natural history of TRPV4-Related disorders: From skeletal dysplasia to neuromuscular phenotype
16. Genetic disorders with symptoms mimicking rheumatologic diseases: A single-center retrospective study
17. İngiltere Premier Lig Futbol Kulüplerinin Sosyal Değişim Uygulamalarının Spor ve Sosyal Hizmet Perspektifinde İncelenmesi.
18. A Novel ZBTB20 Variant in a Patient with Primrose Syndrome: A Rare Clinical Entity with Distinctive Features.
19. Portfolio Optimization via a Surrogate Risk Measure: Conditional Desirability Value at Risk (CDVaR)
20. Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families
21. A Long-Term Follow-Up of a Patient with a Novel PORCN Variant and Additional Clinical Features
22. Intrafamilial variability of XYLT2-related spondyloocular syndrome
23. Hyperphosphatasia with mental retardation syndrome type 4 In two siblings-expanding the phenotypic and mutational spectrum
24. A novel NKX3-2 mutation associated with perinatal lethal phenotype of spondylo-megaepiphyseal-metaphyseal dysplasia in a neonate
25. Fragile x-associated premature ovarian failure in a large Turkish cohort: Findings of Hacettepe Fragile X Registry
26. Echocardiographic evaluation from a different perspective in asthmatic patients
27. Okul Öncesi Öğretmenlerinin Görüşlerine Göre Okul Müdürlerinin Güçlendirici Liderlik Yeterliklerinin Belirlenmesi
28. Madde Güçlüklerinin Tahmin Edilmesinde Uzman Görüşleri ve ChatGPT Performansının Karşılaştırılması
29. Low Earth Orbit-Based Small-Size Constellation Satellite System Design For Communication Between Türkiye and Antarctica
30. HERC1 mutations in idiopathic intellectual disability
31. Portfolio Optimization via a Surrogate Risk Measure: Conditional Desirability Value at Risk (CDVaR)
32. Gorlin Syndrome in Eleven Patients
33. Obstrüktis Uyku Apnesi Olan Hastalarda Hastalık Şiddeti ile CRP/Prealbümin Oranı Arasındaki İlişki
34. Matematik Başarısında Grup Farklılıklarının İncelenmesi: Açıklayıcı Madde Tepki Modeli Uygulaması
35. Ergenler İçin Sosyal Medya Bağımlılığı Ölçeği’nin Cinsiyet ve Okul Kademesi Değişkenleri Açısından Ölçme Değişmezliğinin İncelenmesi
36. Examining The Measurement Invariance of The Social Media Addiction Scale For Adolescents in Terms of Gender and Grade Level Variables
37. A Long-Term Follow-Up of a Patient with a Novel PORCNVariant and Additional Clinical Features
38. A Novel ZBTB20Variant in a Patient with Primrose Syndrome: A Rare Clinical Entity with Distinctive Features
39. Arsenik ile oksidatif stres oluşturan ratlarda karvakrolün etkisinin araştırılması
40. A novel biallelicCRIPTvariant in a patient with short stature, microcephaly, and distinctive facial features
41. Obstructive sleep apnea in children with Down syndrome: is it possible to predict severe apnea?
42. The Influence of Culture on Memory
43. The Effects of Re-functioning to the Historical Houses
44. Effects of Functional Change on Historical Houses: The example of 'Alsancak Levantine Houses'
45. A Life-Threatening Complication in a Patient with Ehlers-Danlos Syndrome Musculocontractural Type
46. Novel homozygous mutations in the osteoprotegerin gene TNFRSF11B in two unrelated patients with juvenile Paget's disease
47. Dermatologic Manifestations of Colchicine Intoxication
48. Spondyloepimetaphyseal dysplasia <scp>EXTL3‐deficient</scp> type: Long‐term <scp>follow‐up</scp> and review of the literature
49. Homozygous indel mutation in CDH11 as the probable cause of Elsahy–Waters syndrome
50. Earthquake parameters affecting the performance of an RC frame with friction damper
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