鍾 明怡

Medicine & Life Sciences

1. Spinocerebellar Ataxias 100%
2. Genes 92%
3. Genotype 87%
4. N,N-dimethylarginine 79%
5. Chromosomes 66%
6. Tetralogy of Fallot 55%
7. Renal Dialysis 55%
8. Arteriovenous Fistula 53%
9. Heme Oxygenase-1 49%
10. Microsatellite Repeats 45%
11. Attention Deficit Disorder with Hyperactivity 42%
12. Alleles 42%
13. Squamous Cell Carcinoma 35%
14. dimethylargininase 34%
15. Mutation 34%
16. Loss of Heterozygosity 30%
17. Chromosomes, Human, Pair 22 29%
18. Trinucleotide Repeats 28%
19. Restless Legs Syndrome 27%
20. Genetic Polymorphisms 27%
21. Organophosphates 26%
22. Matrix Metalloproteinase 1 25%
23. Migraine Disorders 24%
24. Ataxin-1 24%
25. Single Nucleotide Polymorphism 24%
26. Blood Cells 24%
27. Pesticides 23%
28. Spinocerebellar ataxia 22 23%
29. Areca 21%
30. Dopamine D4 Receptors 21%
31. Exons 20%
32. 2-((2-((dimethylamino)methyl)phenyl)thio)-5-iodophenylamine 20%
33. Chromosome Deletion 20%
34. Interleukin-4 19%
35. Organism Cloning 19%
36. Haplotypes 19%
37. Neoplasms 19%
38. Child 19%
39. Yeast Artificial Chromosomes 19%
40. Glycine N-Methyltransferase 18%
41. Taiwan 18%
42. Familial Exudative Vitreoretinopathies 18%
43. retinol dehydrogenase 17%
44. Messenger RNA 17%
45. Cerebellar Ataxia 17%
46. Endometrial Stromal Tumors 17%
47. Argininosuccinate Synthase 17%
48. Allelic Imbalance 17%