Lisa Kratz

Medicine & Life Sciences

1. Smith-Lemli-Opitz Syndrome 100%
2. Sterols 67%
3. Cholesterol 55%
4. Desmosterolosis 29%
5. Chondrodysplasia Punctata 27%
6. Prenatal Diagnosis 20%
7. 7-dehydrocholesterol 19%
8. Mutation 18%
9. Genes 16%
10. Oxidoreductases 15%
11. dehydropregnanetriol 14%
12. dehydroestriol 14%
13. lamin B receptor 14%
14. Hydroxysteroids 14%
15. Sitosterolemia 13%
16. Isomerases 13%
17. methylsterol monooxygenase 12%
18. Rett Syndrome 10%
19. Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 10%
20. Extremities 10%
21. Urine 10%
22. Ichthyosis 10%
23. Steroids 9%
24. Simvastatin 9%
25. Desmosterol 9%
26. Mothers 9%
27. Restriction Fragment Length Polymorphisms 9%
28. Microcephaly 8%
29. Enchondromatosis 8%
30. Leucine-tRNA Ligase 8%
31. lathosterol delta-5-dehydrogenase 8%
32. delta(8)-delta(7)-sterol isomerase 8%
33. Phenotype 8%
34. Lathosterolosis 8%
35. Lanosterol 8%
36. Costeff optic atrophy syndrome 8%
37. Autism Spectrum Disorder 8%
38. Pregnancy 7%
39. Rhizomelic Chondrodysplasia Punctata 7%
40. Plasmalogens 7%
41. Brain Injuries 7%
42. Choline 7%
43. ErbB Receptors 7%
44. Peroxisomal Disorders 7%
45. Cataract 7%
46. Fetus 7%
47. Antley-Bixler Syndrome Phenotype 7%
48. Molybdenum cofactor deficiency 7%
49. Phytosterols 7%
50. Glutaryl-CoA Dehydrogenase 7%