Gail Stetten

Medicine & Life Sciences

1. Chromosomes 100%
2. Karyotype 79%
3. Chromosomes, Human, Pair 21 67%
4. Mosaicism 64%
5. Fluorescence In Situ Hybridization 60%
6. Cytogenetics 57%
7. Fetus 52%
8. X Chromosome 47%
9. Prenatal Diagnosis 44%
10. Amniocentesis 42%
11. Bisbenzimidazole 40%
12. Phenotype 40%
13. Trisomy Chromosome 20 37%
14. DNA 34%
15. Genes 32%
16. Ring Chromosomes 31%
17. Cytogenetic Analysis 31%
18. Chromosome 21 ring 30%
19. Pregnancy 28%
20. Trisomy 7q Chromosome 7 26%
21. Chromosome Aberrations 26%
22. Turner Syndrome 26%
23. Comparative Genomic Hybridization 25%
24. Y Chromosome 25%
25. Centromere 24%
26. Karyotyping 23%
27. Ovotesticular Disorders of Sex Development 23%
28. Chorionic Villi 23%
29. Cell Line 22%
30. Hematopoietic Stem Cell Transplantation 22%
31. Chimerism 22%
32. Spontaneous Abortion 21%
33. Chromosome Painting 21%
34. Trisomy 18 Syndrome 21%
35. Bromodeoxyuridine 21%
36. Yeast Artificial Chromosomes 20%
37. X Chromosome Inactivation 20%
38. Lymphocytes 20%
39. Adrenoleukodystrophy 20%
40. Human Chromosomes 19%
41. Down Syndrome 19%
42. Chromosomes, Human, Pair 18 19%
43. Genetic Markers 18%
44. Canidae 18%
45. Chromosomes, Human, Pair 7 17%
46. Amniotic Fluid 17%
47. Chromosomes, Human, Pair 13 16%
48. Clone Cells 15%