倉橋 浩樹

Medicine & Life Sciences

1. Alleles 26%
2. Aneuploidy 24%
3. Autosomal Recessive Polycystic Kidney 16%
4. Chromosome Pairing 20%
5. Chromosome Segregation 17%
6. Chromosomes 56%
7. Chromosomes, Human, Pair 22 48%
8. Chromothripsis 17%
9. Classical Lissencephalies and Subcortical Band Heterotopias 16%
10. Cosmids 25%
11. Cruciform DNA 24%
12. Delayed Graft Function 18%
13. DiGeorge Syndrome 33%
14. DNA 26%
15. Down Syndrome 15%
16. Exons 28%
17. Fluorescence In Situ Hybridization 22%
18. Genes 100%
19. Genetic Testing 23%
20. Genetic Translocation 31%
21. Genetic Variation 16%
22. Genomic Instability 34%
23. Genotype 16%
24. Haplotypes 16%
25. Human Chromosomes 17%
26. Human Genome 19%
27. Human Herpesvirus 6 45%
28. Incontinentia Pigmenti 15%
29. Indoleamine-Pyrrole 2,3,-Dioxygenase 18%
30. Kidney 31%
31. Kidney Transplantation 17%
32. Lipocalin-2 17%
33. Loss of Heterozygosity 17%
34. Meiosis 39%
35. Mosaicism 30%
36. Mothers 32%
37. Muscular Dystrophies 16%
38. Mutation 68%
39. Oocytes 20%
40. Placenta 30%
41. Polycystic Kidney Diseases 20%
42. Polymerase Chain Reaction 23%
43. Pre-Eclampsia 53%
44. Pregnancy 27%
45. Prophase 17%
46. Proteins 24%
47. Spermatozoa 29%
48. Tissue Donors 20%
49. Transient Myeloproliferative Syndrome 17%
50. Walker-Warburg Syndrome 37%