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2. Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder

3. Loss-of-function in RBBP5 results in a syndromic neurodevelopmental disorder associated with microcephaly

5. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

6. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

7. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

8. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

9. De novo variants in DENND5B cause a neurodevelopmental disorder

10. Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

11. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

14. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

15. Geleneksel sinterleme ve spark plazma sinterleme yöntemlerinin nanokristal yapılı CoCrFeNi yüksek entropili alaşımın mikroyapısal özellikleri ve sertliği üzerine etkilerinin araştırılması

18. De novo variants in DENND5B cause a neurodevelopmental disorder

19. Intra-articular administration of extra-virgin olive oil in degenerative osteoarthritis.

20. Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss.

22. ADAMTSL2 mutations determine the phenotypic severity in Geleophysic Dysplasia

23. RExPRT: a machine learning tool to predict pathogenicity of tandem repeat loci

24. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

25. Genetic Landscape of Hearing Loss in the Caribbean: A Narrative Review.

26. Readability of online educational materials for brainstem implants: An assessment.

27. Recurrent ATP1A1 variant Gly903Arg causes developmental delay, intellectual disability, and autism.

28. Two novel heterozygous exonic deletions lead to Chanarin–Dorfman syndrome in a patient with congenital ichthyosis, sensorineural hearing loss, and liver dysfunction.

32. Loss-of-function in RBBP5results in a syndromic neurodevelopmental disorder associated with microcephaly

33. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

34. Dominant missense variants in SREBF2are associated with complex dermatological, neurological, and skeletal abnormalities

35. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

36. Biallelic CRELD1variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections

37. Identifying DNA Variants in a Turkish Cohort with Inner Ear Anomalies

38. The Effect of Thymoquinone on Acoustic Trauma-Induced Hearing Loss in Rats.

39. Advancing Equity in Rare Disease Research: Insights From the Undiagnosed Disease Network.

40. The Frequency of Presence of the Infraorbital Canal in the Maxillary Sinus and its Clinical Importance.

42. A Scopus-Based Bibliometric Analysis of the Journal of Craniofacial Surgery From 1990 to 2023.

43. Journal Metrics of the Journal of Craniofacial Surgery: An Analysis Based on the Journal Citation Report 2024.

45. Evaluating the Success of ChatGPT in Addressing Patient Questions Concerning Thyroid Surgery.

46. Human Organoids for Rapid Validation of Gene Variants Linked to Cochlear Malformations.

47. EFEMP1 haploinsufficiency causes a Marfan-like hereditary connective tissue disorder.

48. Triple Primary Cancers: An Analysis of Genetic and Environmental Factors.

49. SNUPN deficiency causes a recessive muscular dystrophy due to RNA mis-splicing and ECM dysregulation.

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