Identification and functional investigation of genes in patients with inherited bleeding disorders

Medicine & Life Sciences

1. Blood Platelets 100%
2. Hemorrhage 50%
3. Scott Syndrome 35%
4. Genes 25%
5. Whole Exome Sequencing 24%
6. Thrombomodulin 24%
7. Tropomyosin 23%
8. Menorrhagia 23%
9. Computational Biology 22%
10. Platelet Count 21%
11. Genomics 18%
12. Natural History 18%
13. High-Throughput Nucleotide Sequencing 17%
14. Thrombocytopenia 17%
15. Megakaryocytes 11%
16. 5' Untranslated Regions 10%
17. Phosphatidylserines 10%
18. Mutation 10%
19. Thrombin 9%
20. Point Mutation 8%
21. Thrombocytopenia chromosome breakage 8%
22. Inborn Genetic Diseases 7%
23. Disease Susceptibility 7%
24. GATA2 Deficiency 6%
25. Platelet Aggregation 5%
26. Blood Coagulation 5%