Tord Jonson

Medicin och livsvetenskap

1. Neoplasms 100%
2. Telomere 97%
3. Pancreatic Carcinoma 93%
4. Chromosomal Instability 80%
5. Chromosomes 78%
6. Chromosome Aberrations 70%
7. Phenotype 69%
8. Mutation 66%
9. Hypotonia-Cystinuria Syndrome 62%
10. Genes 62%
11. Ring Chromosomes 54%
12. Uniparental Disomy 52%
13. Genome 52%
14. Congenital Hyperinsulinism 44%
15. Fluorescence In Situ Hybridization 42%
16. Cell Line 41%
17. Giant Cell Tumor of Bone 41%
18. Chromosomes, Human, Pair 12 38%
19. Transforming Growth Factor beta Receptors 38%
20. Enteric Nervous System 38%
21. Polymerase Chain Reaction 37%
22. Hirschsprung Disease 37%
23. Liposarcoma 37%
24. Single Nucleotide Polymorphism 36%
25. Genetic Variation 35%
26. Telomerase 35%
27. Wilms Tumor 34%
28. Gene Dosage 34%
29. Rhabdomyosarcoma 34%
30. Genetic Heterogeneity 34%
31. Neurodevelopmental Disorders 33%
32. Loss of Heterozygosity 33%
33. Sensorineural Hearing Loss 32%
34. Beckwith-Wiedemann Syndrome 32%
35. Whole Exome Sequencing 31%
36. DNA Fragmentation 30%
37. Gene Expression 28%
38. Neuroblastoma 28%
39. Mitosis 28%
40. Pediatrics 28%
41. Precursor Cell Lymphoblastic Leukemia-Lymphoma 28%
42. Acute Myeloid Leukemia 27%
43. Neck 27%
44. Anaphase 27%
45. Transforming Growth Factor beta 26%
46. Heterografts 25%
47. Dissection 24%
48. Transforming Growth Factor-beta Type II Receptors 24%
49. Carcinoma 22%
50. Expressed Sequence Tags 21%