Interactive Case Study Companion
1 - Aorta, cystic medionecrosis - Very low power (Glass slide 114)
2 - Aorta, cystic medionecrosis - Medium power (Glass slide 114)
3 - Aorta, cystic medionecrosis, elastic stain - Medium power
4 - Heart, glycogen storage disease - Gross, cut surfaces
5 - Heart, glycogen storage disease - Medium power (Glass slide 8)
6 - Heart, glycogen storage disease - High power (Glass slide 8)
7 - Spleen, Gaucher disease - Medium power (Glass slide 11)
8 - Spleen, Gaucher disease - High power (Glass slide 11)
9 - Bone marrow smear, Gaucher disease - High power
10 - Pancreas, cystic fibrosis - Gross, cut surface
11 - Pancreas, cystic fibrosis - Low power
12 - Trisomy 21 - Karyotype
13 - Trisomy 21, phenotype - Illustration
14 - Trisomy 21 - Clinical presentation
15 - Trisomy 18 - Karyotype
16 - Trisomy 18, phenotype - Illustration
17 - Trisomy 18 - Clinical presentation
18 - Trisomy 13 - Karyotype
19 - Trisomy 13, phenotype - Illustration
20 - Trisomy 13 - Clinical presentation
21 - Turner syndrome (monosomy X) - Karyotype
22 - Turner syndrome (isochromosome Xq, resulting in monosomy Xp) - Karyotype
23 - Turner syndrome, phenotype - Illustration
24 - Turner syndrome - Clinical presentation
25 - The fragile X chromosome in fragile X syndrome - Illustration
26 - Fragile X syndrome - Clinical presentation
27 - Molecular diagnosis of fragile X premutation and full mutation - Schematic
28 - Prader-Willi syndrome - Clinical presentation
29 - Angelman syndrome - Clinical presentation
30 - Deletion of band q12 in one #15 chromosome (the chromosome on the right) - Illustration
31 - Fluorescence in situ hybridization (FISH) of DNA probes to metaphase chromosomes