Pt. I. Basic concepts and background -- Ch. 1. History of clinical cytogenetics -- Ch. 2. DNA, chromosomes, and cell division -- Ch. 3. Human chromosome nomenclature: an overview and definition of terms -- Pt. II. Examining and analyzing chromosomes -- Ch. 4. Basic laboratory procedures -- Ch. 5. Microscopy and photomicrography -- Ch. 6. Quality control and quality assurance -- Ch. 7. Automation in the cytogenetics laboratory Pt. III. Clinical cytogenetics-- Ch. 8. Autosomal aneuploidy -- Ch. 9. Structural chromosome rearrangements -- Ch. 10. Sex chromosomes and sex chromosome abnormalities -- Ch. 11. Prenatal cytogenetics -- Ch. 12. Cytogenetics of spontaneous abortion -- Ch. 13. Cancer cytogenetics -- Pt. IV. Beyond chromosomes -- Ch. 14. Fragile X: from cytogenetics to molecular genetics -- Ch. 15. Fluorescence in situ hybridization -- Ch. 16. Genomic imprinting and uniparental disomy -- Ch. 17. Genetic counseling.
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