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34 results on '"Yaldiz, Burcu"'

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1. Comprehensive reanalysis for CNVs in ES data from unsolved rare disease cases results in new diagnoses

2. Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing

5. Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples

6. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

7. Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant

8. Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing

9. Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

10. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

11. Twist exome capture allows for lower average sequence coverage in clinical exome sequencing

12. Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples

13. Solving unsolved rare neurological diseases-a Solve-RD viewpoint

14. A QUALITATIVE ANALYSIS ON THE LEVEL OF SATISFACTION OF THE TRAINEES ATTENDING THE COURSES IN PUBLIC EDUCATION CENTERS: THE EXAMPLE OF BANDIRMA PUBLIC EDUCATION CENTER

16. MESLEK AŞKI VE İŞ PERFORMANSI İLİŞKİSİ SAĞLIK ÇALIŞANLARI ÜZERİNE BİR ARAŞTIRMA

17. Correction to: Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

18. Decellularised extracellular matrix-based biomaterials for repair and regeneration of central nervous system

19. Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant

21. Solving patients with rare diseases through programmatic reanalysis of genome-phenome data

22. Correction: Solving unsolved rare neurological diseases : A Solve-RD viewpoint

23. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

24. Advances in microfluidic synthesis and coupling with synchrotron SAXS for continuous production and real-time structural characterization of nano-self-assemblies

27. Konaklama öğretmenlerinin özel eğitim alanı ile ilgili yaşadıkları güçlüklerin belirlenmesi ve kat hizmetleri eğitim modülü önerisi

28. Konaklama Öğretmenlerinin Özel Eğitim Alanında Zorlandığı Konular, MEB'e ve Eğitim Fakültelerine Öneriler.

29. Investigation of structural properties of methylated human promoter regions in terms of DNA helical rise

30. Analysis of the log-domain filters designed with E-cells

32. A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing

33. Genome-wide variant calling in reanalysis of exome sequencing data uncovered a pathogenic TUBB3 variant.

34. Decellularised extracellular matrix-based biomaterials for repair and regeneration of central nervous system.

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