Includes bibliographical reference and index.

DNA structure and function
Genetic variation
Patterns of inheritance
The human genome
Multifactorial inheritance
Cell division and chromosomes
Population genetics
Cancer genetics
Chromosome translocation
Molecular diagnosis
Newborn screening
Developmental genetics
Carrier screening
Genetic risk assessment
Genetic testing for risk of cancer
Pharmacogenetics
Treatment of genetic disorders

This text clearly explains the key principles needed by medical and health sciences students, from the basis of molecular genetics, to clinical applications used in the treatment of both rare and common conditions. A newly expanded Part 1, Basic Principles of Human Genetics, focuses on introducing the reader to key concepts such as Mendelian principles, DNA replication and gene expression. Part 2, Genetics and Genomics in Medical Practice, uses case scenarios to help you engage with current genetic practice. Now featuring full-color diagrams, Human Genetics and Genomics has been rigorously updated to reflect today's genetics teaching, and includes updated discussion of genetic risk assessment, single gene disorders and therapeutics. Key learning features include: Clinical snapshots to help relate science to practice 'Hot topics' boxes that focus on the latest developments in testing, assessment and treatment 'Ethical issues' boxes to prompt further thought and discussion on the implications of genetic developments 'Sources of information' boxes to assist with the practicalities of clinical research and information provision.