The following images are present:

Basic Genetics

1. Cell cycle and mitosis, diagram
2. Meiosis, table
3. Types of DNA
4. Genes
5. Gene mutations

Patterns of Inheritance

6. Patterns of Inheritance
7. Autosomal recessive - cystic fibrosis, sickle cell anemia
8. Autosomal dominant - osteogenesis imperfecta, Marfan syndrome
9. Autosomal dominant, reduced penetrance - Huntington disease
10. Autosomal dominant, spontaneous new mutation - achondroplasia
11. X-linked recessive - hemophilia A
12. X-linked dominant - fragile X syndrome
13. Mitochondrial inheritance - MELAS
14. Germline mosaicism - neurofibromatosis 1
15. Dosage sensitivity - familial hypercholesterolemia
16. Imprinting
17. Multifactorial inheritance
18. Teratogens - fetal alcohol syndrome
19. Neoplasia and genetics, diagrams
20. DNA repair
21. RFLP analysis

Chromosome Analysis

22. Normal chromosome at metaphase, diagram
23. Normal male karyotype, G-banding, diagram
24. Normal male karyotype, high resolution banding, diagram
25. Chromosomal abnormalities, diagram
26. Chromosomal abnormalities with karyotypes, table
27. Fluorescence in situ hybridization (FISH), diagram
28. Fluorescence in situ hybridization (FISH), abnormalities, diagram
29. Fluorescence in situ hybridization (FISH), abnormalities, diagram
30. Normal female 46, XX karyotype

Chromosomal Abnormalities

31. Trisomy 21 (47, XY, +21) karyotype
32. Down syndrome, facial features, gross
33. External ear, low set and simplified, gross
34. Hand, abnormal transverse crease, gross
35. Trisomy 13 (47, XX, +13) karyotype
36. Cleft lip with trisomy 13, gross
37. Polydactyly, with trisomy 13, gross
38. Polydactyly, with trisomy 13, gross
39. Cyclopia with trisomy 13, gross
40. Holoprosencephaly with trisomy 13, gross
41. Trisomy 18 (47, XY, +18) karyotype
42. Clenched hand with trisomy 18, gross
43. Clenched hand with trisomy 18, gross
44. Monosomy X, or Turner syndrome (45, X) karyotype
45. Monosomy X, or Turner syndrome, streak ovaries in adult, gross
46. Massive fetal hydrops with monosomy X, or Turner syndrome, gross
47. Cystic hygroma with monosomy X, or Turner syndrome, gross
48. Cystic hygroma with monosomy X, or Turner syndrome, gross
49. Cystic hygroma with monosomy X, or Turner syndrome, gross
50. Cystic hygroma with monosomy X, or Turner syndrome, microscopic
51. Trisomy 16 with single X chromosome (46, X, +16) karyotype
52. Chromosomal translocation, 14 to 13, balanced karyotype
53. Wolf-Hirschhorn (4p-) syndrome karyotype
54. Klinefelter syndrome (47, XXY) karyotype
55. XYY male (47, XYY) karyotype, diagram
56. Triple X female (47, XXX) karyotype, diagram
57. Fragile X syndrome, karyotype, diagram
58. Marker chromosome, karyotype, diagram
59. Philadelphia chromosome (9;22 translocation) karyotype with chronic myelogenous leukemia
60. DiGeorge anomaly, thymus, with 22q11 deletion syndrome
61. Triploidy (69, XXY) by flow cytometry
62. Triploidy (69, XXY) karyotype, diagram
63. Triploidy, with characteristic 3-4 syndactyly of fetal hand, gross