Steve Mumm

Medicine & Life Sciences

1. Hypophosphatasia 100%
2. Mutation 80%
3. Alkaline Phosphatase 63%
4. Genes 57%
5. Bone and Bones 52%
6. Hyperostosis corticalis deformans juvenilis 46%
7. Isoenzymes 43%
8. Osteosclerosis 37%
9. Adult Hypophosphatasia 33%
10. Sequence Tagged Sites 31%
11. Exons 30%
12. Osteopetrosis 30%
13. Serum 29%
14. Infantile Hypophosphatasia 28%
15. Osteoprotegerin 28%
16. Osteitis Deformans 27%
17. Yeast Artificial Chromosomes 26%
18. Missense Mutation 25%
19. Familial Hypophosphatemic Rickets 24%
20. Bone Density 23%
21. Dysosteosclerosis 22%
22. Bone Remodeling 22%
23. X Chromosome 21%
24. Osteochondrodysplasias 21%
25. Bone Diseases 20%
26. Osteoclasts 19%
27. Rickets 18%
28. Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia 17%
29. Osteogenesis 16%
30. Rous sarcoma virus 16%
31. Diphosphonates 16%
32. Clone Cells 15%
33. Teriparatide 15%
34. Middle Aged 15%
35. X Chromosome Inactivation 15%
36. Osteopoikilosis 14%
37. Childhood Hypophosphatasia 14%
38. Loss of Function Mutation 14%
39. Integrases 14%
40. Base Pairing 13%
41. Buschke-Ollendorff syndrome 13%
42. Hereditary expansile Polyostotic osteolytic dysplasia 13%
43. Metabolic Bone Diseases 13%
44. DNA 13%
45. Osteomalacia 13%
46. Hajdu-Cheney Syndrome 13%
47. Spine 13%
48. Camurati-Engelmann Syndrome 12%
49. RANK Ligand 12%
50. Muscular Diseases 12%