Medicine & Life Sciences

1. Neurofibromatosis 1 100%
2. Mutation 79%
3. Plexiform Neurofibroma 75%
4. Genes 50%
5. pirfenidone 48%
6. Neurofibroma 45%
7. Phenotype 43%
8. Neurofibromatoses 41%
9. Congenital Disorders of Glycosylation 39%
10. Intellectual Disability 33%
11. Neoplasms 30%
12. Child 27%
13. Whole Exome Sequencing 25%
14. Muscle Hypotonia 23%
15. Schwannomatosis 23%
16. Lipectomy 20%
17. Legius syndrome 20%
18. Mannose-6-Phosphate Isomerase 19%
19. Precision Medicine 19%
20. Chromosomes 18%
21. Mannose-Binding Protein Deficiency 17%
22. Pheochromocytoma 17%
23. Glycosylation 17%
24. Missense Mutation 17%
25. Fluorescence In Situ Hybridization 16%
26. Smith-Lemli-Opitz Syndrome 16%
27. Neurilemmoma 16%
28. Ornithine Carbamoyltransferase Deficiency Disease 16%
29. Butyryl-CoA Dehydrogenase 16%
30. Dolichols 16%
31. Neurofibromatosis 2 16%
32. Genetic Association Studies 16%
33. Mosaicism 15%
34. Alleles 15%
35. Genetic Testing 15%
36. Mothers 15%
37. Cerebellar Ataxia 14%
38. Turner Syndrome 13%
39. Exons 12%
40. Megalencephaly 12%
41. Therapeutics 12%
42. Kennerknecht Sorgo Oberhoffer syndrome 12%
43. Growth 12%
44. Holoprosencephaly, Ectrodactyly, and Bilateral Cleft Lip-Palate 11%
45. Magnetic Resonance Imaging 11%
46. Short chain Acyl CoA dehydrogenase deficiency 11%
47. Type 2 Oto-palato-digital syndrome 11%
48. Pulmonary Valve Stenosis 11%
49. Polyprenols 11%