Since its debut in 1966, Thompson and Thompson Genetics and Genomics in Medicine has been an indispensable companion for students and trainees in the medical and genetic fields. This ninth edition continues to provide an unrivaled exploration of human genetics and genomics, making it a well-loved resource for countless learners.
Key Features:
Comprehensive Coverage: Delve into the fascinating world of genomes in biology and medicine, copy number and structural genomic variation, novel discoveries, latest technology, and new genetic diagnoses.
Clinical Case Studies: Over 40 real-life clinical case studies offer insights into the challenges of variable expression, pleiotropy, and complex disorders, guiding readers through new diagnostic strategies.
Richly Illustrated: Enjoy a visually captivating experience with full-color text, updated line diagrams, clinical photos, and striking images of individuals living with genetic conditions.
Interactive Learning: Test your knowledge with end-of-chapter questions and comprehensive answers, allowing you to apply the material to practical scenarios and prepare for examinations. USMLE-style and multiple-choice questions are available in the eBook version.
Enhanced eBook: Access the enriched eBook version, offering full-text searchability, customizable content, note-taking, highlight features, and an option for content to be read aloud.
What’s New in the 9th Edition:
Updated Clinical Cases: Fresh clinical cases, supported by heartwarming photography from Positive Exposure, provide relevant context and real-world perspectives.
Growing Role of Sequencing and Functional Assays: Learn about the increasing significance of sequencing and novel functional assays in the diagnosis and screening of genetic conditions.
Epigenetics Chapter: Discover the latest advancements in the field of epigenetics, a crucial aspect of genetics.
Clearer Terminology: Updated terminology aligns with contemporary and evolving guidelines, ensuring clarity and precision.
Diverse Populations: Gain insights into the use and need for genetic information from diverse populations, including unique indigenous and founder populations, for diagnosis and management.
