Marianne Lodahl

Medicine & Life Sciences

1. Agammaglobulinemia 9%
2. Age of Onset 26%
3. Animal Models 7%
4. Arginine 9%
5. Autosomal Dominant 10 Deafness 45%
6. Central Nervous System 7%
7. CHARGE Syndrome 80%
8. Chromatin Assembly and Disassembly 11%
9. Chromosome Aberrations 13%
10. Congresses 8%
11. Counselors 9%
12. Dilated Cardiomyopathy 15%
13. DNA-Binding Proteins 11%
14. Dystonia 58%
15. Ear 8%
16. Ectrodactyly 81%
17. Eosine Yellowish-(YS) 7%
18. Eye 10%
19. Frameshift Mutation 73%
20. Gene Deletion 15%
21. Genes 25%
22. Genetic Association Studies 7%
23. Genetic Counseling 54%
24. Haploinsufficiency 9%
25. Hearing Loss 81%
26. Hematoxylin 7%
27. Homologous Recombination 8%
28. Leber's Hereditary Optic Atrophy 42%
29. Loss of Function Mutation 11%
30. Mohr-Tranebjaerg syndrome 100%
31. Mutation 51%
32. Myelin Basic Protein 17%
33. Nonsense Codon 11%
34. Nonsyndromic Deafness 10%
35. Nose 13%
36. Nuclear Family 7%
37. Nucleic Acid Regulatory Sequences 8%
38. Nucleic Acid Repetitive Sequences 8%
39. Optic Atrophy 17%
40. Optic Nerve 51%
41. Optic Nerve Diseases 17%
42. Orofaciodigital Syndromes 85%
43. Penetrance 16%
44. Population Biological Variation 61%
45. Psychological Imprinting 10%
46. Retina 24%
47. Retinal Ganglion Cells 8%
48. Spain 8%
49. Terminator Codon 11%
50. Wolfram Syndrome 82%