Jens Michael Hertz

Medicin og biovidenskab

1. Hereditary Nephritis 100%
2. Mutation 79%
3. Genes 53%
4. Klinefelter Syndrome 49%
5. Exons 34%
6. Anhidrotic Ectodermal Dysplasia 1 32%
7. X Chromosome Inactivation 26%
8. Phenotype 26%
9. Genetic Association Studies 25%
10. Chromosomes 23%
11. Mothers 23%
12. Angelman Syndrome 23%
13. Denmark 23%
14. Molecular Biology 22%
15. Missense Mutation 21%
16. Collagen 20%
17. X Chromosome 19%
18. Nonsense Codon 19%
19. Alleles 17%
20. Hip Dislocation 16%
21. Mosaicism 16%
22. Whole Exome Sequencing 15%
23. Karyotype 15%
24. Myotonic Dystrophy 15%
25. Ectodermal Dysplasia 15%
26. DNA 14%
27. Pycnodysostosis 14%
28. Collagen Type IV 13%
29. Genetic Background 12%
30. Amelogenesis Imperfecta 12%
31. Polymerase Chain Reaction 12%
32. First Pregnancy Trimester 12%
33. Fetus 12%
34. Ring Chromosomes 12%
35. Hematuria 11%
36. Single-Stranded Conformational Polymorphism 11%
37. Mutation Rate 11%
38. Tooth 11%
39. Glycine 11%
40. Charcot-Marie-Tooth Disease 10%
41. Prenatal Diagnosis 10%
42. Spinal Muscular Atrophy 10%
43. Proteinuria 10%
44. Haplotypes 10%
45. Kidney 10%
46. Cytogenetic Analysis 10%
47. Parkinson Disease 10%
48. Renal Insufficiency 10%
49. Bothnian type Diffuse palmoplantar keratoderma 9%
50. Genetic Testing 9%