Emilia Stellacci

Medicine & Life Sciences

1. Primrose syndrome 100%
2. Spondyloepimetaphyseal Dysplasia With Joint Laxity 97%
3. Phenotype 73%
4. Intellectual Disability 64%
5. Mutation 60%
6. Chromosome 1p36 Deletion Syndrome 43%
7. tRNA nucleotidyltransferase 41%
8. Al-Gazali Syndrome 35%
9. Tarsal Bones 34%
10. Zinc Fingers 34%
11. Developmental Bone Disease 34%
12. Carpal Bones 32%
13. Progeroid form Ehlers-Danlos syndrome 32%
14. STAT1 Transcription Factor 31%
15. Organoids 29%
16. Haploinsufficiency 29%
17. Etanercept 28%
18. Hip Dislocation 27%
19. Transducers 27%
20. Neurodevelopmental Disorders 26%
21. Sensorineural Hearing Loss 25%
22. Germ-Line Mutation 25%
23. X Chromosome 25%
24. Regenerative Medicine 24%
25. Guanosine Triphosphate 24%
26. Exome 23%
27. Missense Mutation 23%
28. Growth and Development 23%
29. Galactosyltransferases 22%
30. Amino Acid Substitution 21%
31. Megalencephaly 21%
32. Ehlers-Danlos Syndrome 21%
33. Cataract 21%
34. Pathologic Dilatations 19%
35. Exons 18%
36. Nucleotides 18%
37. Transcription Factors 17%
38. Proteins 16%
39. Cell Membrane 16%
40. Glycosaminoglycans 16%
41. Joints 16%
42. Neoplasms 14%
43. Bone and Bones 13%
44. Dilatation 12%
45. Kidney 12%
46. Genes 12%
47. Growth 11%
48. Insulin 10%
49. Kidney Neoplasms 9%
50. Glucose 9%