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Showing papers on "Genomics published in 1992"


Book
01 Jan 1992
TL;DR: This book discusses life as Interacting Molecules, application of Human Genetics: Genetic Testing, Gene Therapy, and DNA Fingerprinting, and Genomics: Using Whole Genomes to Study Life.
Abstract: Chapter 1. Preview: Life as Interacting Molecules. PART I. BASIC MOLECULAR GENETICS. Chapter 2. Structure of DNA: Two Long, Interwound Chains. Chapter 3. Reproducing DNA: Information Transfer from One Generation to the Next. Chapter 4. Gene Expression: Cellular Use of Genetic Information. PART II. MANIPULATION DNA. Chapter 5. Microbial Growth: One-celled Organisms as Tools for Gene Cloning. Chapter 6. Plasmids and Phages: Submicroscopic Parasites Used to Deliver Genes to Cells. Chapter 7. Cutting and Joining DNA: Restriction Endonucleases and Ligases Used to Restructure DNA Molecules. Chapter 8. Using Complementary Base Pairing: Hybridization, Probes, and Amplification using PCR. Chapter 9. Cloning Genes: Isolation of a Hemoglobin Gene. Chapter 10. Using Cloned Genes: Gene Structure, Expression Vectors, and Gene Function. PART III. MODERN MOLECULAR GENETICS. Chapter 11. Beyond the Central Dogma: A Sampling of Insights Derived from Gene Cloning. Chapter 12. Retroviruses: AIDS and Gene Delivery. Chapter 13. Cancer Genes: The Loss of Growth Control. PART IV: HUMAN GENETICS. Chapter 14. Heredity: Pattern of Inheritance and Genetic Instability. Chapter 15. Application of Human Genetics: Genetic Testing, Gene Therapy, and DNA Fingerprinting. PART V. WHOLE GENOMES. Chapter 16. Genomics: Using Whole Genomes to Study Life. Additional Reading. Glossary. Abbreviations. Index.

22 citations


Journal ArticleDOI
TL;DR: The societal toll of human dysmorphogenesis and the evident progress with X-linked disorders provide a powerful rationale for the Human Genome Project.
Abstract: A survey of Mendelean Inheritance in Man emphasizes the large Mendelian contribution to human dysmorphogenesis and contrasts single gene conditions with chromosomal disorders. There were 1761 conditions that involved altered morphogenesis (49% of disease entries), including 1040 multiple defect syndromes and 721 inherited single birth defects

14 citations