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2. The impact of the Turkish population variome on the genomic architecture of rare disease traits

4. Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies

6. Contributors

7. The impact of the Turkish (TK) population variome on the genomic architecture of rare disease traits

10. Association between Human Leukocyte Antigen E (HLA-E) Polymorphism, HLA-E Mismatch and Clinical Outcomes in Hematopoietic Cell Transplant for Acute Myeloid Leukemia and Myelodysplastic Syndrome

11. Points to consider in the detection of germline structural variants using next-generation sequencing: A statement of the American College of Medical Genetics and Genomics (ACMG)

12. Human Leukocyte Antigen F (HLA-F) Mismatch Is Associated with Improved Relapse-Free Survival and Overall Survival in Matched Unrelated Donor (MUD) Transplant for Acute Myeloid Leukemia and Myelodysplastic Syndrome

14. Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability

15. Centers for Mendelian Genomics: A decade of facilitating gene discovery

17. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

19. 125 - Human Leukocyte Antigen F (HLA-F) Mismatch Is Associated with Improved Relapse-Free Survival and Overall Survival in Matched Unrelated Donor (MUD) Transplant for Acute Myeloid Leukemia and Myelodysplastic Syndrome

20. DLG2intragenic exonic deletions reinforce the link to neurodevelopmental disorders and suggest a potential association with congenital anomalies and dysmorphism

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