Tord Jonson

Medicine & Life Sciences

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