Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis

1. Introduction
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

Part I. Human Chromosome Methods and Nomenclature

2. Chromosome Heteromorphism
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

3. Frequencies of Heteromorphisms
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

4. Clinical Populations
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

5. Euchromatic Variants
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

6. Chromosome Heteromorphism (Summaries)
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

Part II. Genomics and DNA Polymorphism: Molecular Cytogenetics and DNA Diagnosis

7. Fragile Sites
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

8. Chromosome Variation Detected by Fluorescent In Situ Hybridization (FISH)
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

9. Array-Comparative Genomic Hybridization/Microarray Analysis: Interpretation of Copy Number Variants
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

10. A CNV Catalogue
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

11. Gene and Genome Sequencing: Interpreting Genetic Variation at the Nucleotide Level
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

12. Summary
Herman E. Wyandt, Golder N. Wilson, Vijay S. Tonk

Nyckelord: Biomedicine, Gene Function, General Practice / Family Medicine