Access to the complete content on Oxford Medicine Online requires a subscription or purchase. Public users are able to search the site and view the abstracts for each book and chapter without a subscription.
Please subscribe or login to access full text content.
If you have purchased a print title that contains an access token, please see the token for information about how to register your code.
For questions on access or troubleshooting, please check our FAQs, and if you can't find the answer there, please contact us.
Contents
- 1 Phenotype and Functional Genomics: Introduction
- 2 Evolution
- 3 Genomic Architecture and Copy Number Changes
- 4 Linkage, Association, and Linkage Disequilibrium
- 5 Regulation of Transcription, Splicing and Translation: Impact of Perturbation on Phenotype
- 6 Mitochondria: Genome, Functions, and Phenotype
- 7 Quality Surveillance
- 8 Neurodevelopment and Functional Genomics
- 9 Neurobehavioral Disorders
- 10 Molecular Analyses of Malformation Syndromes
- 11 Multiple Pathways including Environmental Factors that Lead to a Specific Phenotype with Later Onset
- Epilogue
