- ホーム
- > 洋書
- > 英文書
- > Science / Mathematics
Full Description
For decades, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics has served as the ultimate resource for clinicians integrating genetics into medical practice. With nearly 5,000 pages of detailed coverage, contributions from over 250 of the world's most trusted authorities in medical genetics, and a series of 11 volumes available for individual sale, the Seventh Edition of this classic reference includes the latest information on seminal topics such as prenatal diagnosis, genome and exome sequencing, public health genetics, genetic counseling, and management and treatment strategies to complete its coverage of this growing field for medical students, residents, physicians, and researchers involved in the care of patients with genetic conditions.
This comprehensive yet practical resource emphasizes theory and research fundamentals related to applications of medical genetics across the full spectrum of inherited disorders and applications to medicine more broadly. In this volume, leading international contributors examine the genetics of neuropsychiatric, neurological, and neuromuscular disorders, with emphasis on understanding the genetic mechanisms underlying these disorders, diagnostic approaches, and treatment methods that make use of current genomic technologies and translational studies. Here genetic researchers, students, and health professionals will find new and fully revised chapters on the molecular genetics of intellectual disability, dyslexia, autism, schizophrenia, addictive disorders, human epilepsy, sensory disorders, multiple sclerosis, tubular necrosis, and stroke among other conditions. With regular advances in genomic technologies propelling precision medicine into the clinic, Emery and Rimoin's
Principles and Practice of Medical Genetics and Genomics: Seventh Edition bridges the gap between high-level molecular genetics and practical application and serves as an invaluable clinical tool for health professionals and researchers.
Contents
Section 1
1. Fragile X Syndrome and X-linked Intellectual Disability
2. Dyslexia and Related Communication Disorders
3. Attention-Deficit/Hyperactivity Disorder
4. Autism Spectrum Disorders
5. Genetics of Alzheimer Disease
6. Schizophrenia and Affective Disorders
7. Schizophrenia
8. Affective Disorders
9. Addictive Disorders
Section 2
10. Neural Tube Defects
11. Genetic Disorders of Cerebral Cortical Development
12. Genetic Aspects of Human Epilepsy
13. sleep genetics
14. Basal Ganglia Disorders
15. The Hereditary Ataxias
16. Hereditary Spastic Paraplegia
17. Autonomic and Sensory Disorders
18. The Phakomatoses
19. Multiple Sclerosis and Other Demyelinating Disorders
20. neurofibromatosis
21. tubular necrosis
22. Von Hippel-Lindau
23. Genetics of Stroke



