Genetics: From Genes to Genomes (8版)

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【簡介】 Description Genetics: From Genes to Genomes represents a new approach to an undergraduate course in genetics. It reflects the way the authors currently view the molecular basis of life. The eighth edition emphasizes both the core concepts of genetics and the cutting-edge discoveries, modern tools, and analytical methods that will keep the science of genetics moving forward. 【目錄】 Table of Contents Part I Basic Principles: How Traits Are Transmitted 1. Mendel’s Principles of Heredity 2. Extensions to Mendel’s Laws 3. Chromosome and Inheritance 4. Sex Chromosomes 5. Linkage, Recombination, and Gen Mapping Part II What Genes Are and What They Do 6. DNA Structure, Replication, and Recombination 7. Mutation 8. Using Mutations to Study Genes 9. Gene Expression: The Flow of Information from DNA to RNA to Protein Part III Analysis of Genetic Information 10. Digital Analysis of DNA 11. Genome Annotation 12. Analyzing Genomic Variation Part IV How Genes Travel on Chromosomes 13. The Eukaryotic Chromosome 14. Chromosomal Rearrangements 15. Ploidy 16. Bacterial Genetics 17. Organellar Inheritance Part V How Genes Are Regulated 18. Gene Regulation in Prokaryotes 19. Gene Regulation in Eukaryotes 20. Epigenetics Part VI Using Genetics 21. Manipulating the Genomes of Eukaryotes 22. Genetic Analysis of Development 23. The Genetics of Cancer Part VII Beyond the Individual Gene and Genome 24. Variation and Selection in Populations 25. Genetics Analysis of Complex Traits

Clinical Genetics and Genomics at a Glance (1版)

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重量：0.79kg 　頁數：254 裝訂：平裝 　開數：27.5 x 21.8 cm 　印刷：彩色 The market-leading at a Glance series is popular among healthcare students and newly qualified practitioners, for its concise and simple approach and excellent illustrations. Each bite-sized chapter is covered in a double-page spread with clear, easy-to-follow diagrams, supported by succinct explanatory text. Covering a wide range of topics, books in the at a Glance series are ideal as introductory texts for teaching, learning and revision, and are useful throughout university and beyond. Everything you need to know about Clinical Genetics and Genomics … at a Glance! Comprehensive and accessible overview of genetics in clinical practice with a unique systems-based approach Clinical Genetics and Genomics at a Glance combines the clinical and scientific facets of a complex subject in a way that is both accessible and succinct to facilitate the diagnosis, treatment, and management of common genetic conditions. Using the popular “at a Glance” format, this book enables the reader to gain a solid understanding of the practical applications of clinical genetics in different systems. Covering a wide range of topics, this book is perfect for an introduction on the subject texts or for revision purposes and are useful throughout medical school and beyond. Clinical Genetics and Genomics at a Glance uses a systemic approach following all the systems in the body: General topics such as inheritance, cytogenetic and molecular genetic techniques, how to read a genetic test report, and genetic counselling Chapters on key conditions with a genetic basis, organised by body systems, for example: Cardiology topics such as congenital heart disease, ischaemic heart disease, cardiomyopathies, arrhythmias, and sudden cardiac death Dermatology topics such as tuberous sclerosis, Gorlin syndrome, Darier disease, lamellar ichthyosis, mal de meleda, cutaneous porphyria, and epidermolysis bullosa Endocrinology topics such as adrenal gland conditions, androgen insensitivity syndrome, ambiguous sex syndromes, anorchism, Klinefelter syndrome, Turner syndrome, and diabetes mellitus Clinical Genetics and Genomics at a Glance is a helpful learning aid that can be used at various stages of medical training to gain an understanding of the aspects of clinical genetics and the fundamentals behind the specialty. The text also functions as a useful on-ward reference tool for practitioners of all experience levels.

Thompson & Thompson Genetics and Genomics in Medicine (9版)

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重量：1.37kg 　頁數：645 裝訂：平裝 　開數：27.5 x 21.5 cm 　印刷：彩色 紙本+全文電子書(Enhanced Digital Version Included) First published in 1966, Thompson and Thompson Genetics and Genomics in Medicine has become an essential textbook for medical students, genetic counseling students, students in laboratory medicine, and more advanced trainees. With its focus on fundamental principles in human genetics and genomics and their application to medicine, the book has served many as a well-thumbed resource they return to over and over. Such students can continue to depend on this valuable text, joining those in newer fields of genome data analysis for all they need to know about genetics and genomics throughout their basic science training, clinical placements and beyond. Coverage includes new discoveries―such as the functional roles of non-coding RNAs, chromatin regulation and epigenetics―latest technologies, and new diagnoses they are enabling. Under an expanded title, this ninth edition has been completely revised by a new editorial team overseeing a large cadre of contributing authors. Support groups have also assisted to update illustrations featuring beautiful images of those living with genetic conditions. Comprehensive coverage of: genomes in biology and medicine; copy number and structural genomic variation; novel discoveries; latest technology; and new genetic diagnoses Over 40 clinical case studies, capturing the latest challenges of variable expression, pleiotropy, and complex disorders through new diagnostic strategies Full-color text, illustrations, updated line diagrams, and clinical photos End-of-chapter questions and comprehensive answers to challenge the reader to consolidate the material into practice and prepare for examinations USMLE-style and multiple choice questions available as part of the eBook An enhanced eBook version is included with purchase. The eBook allows you to access all the text, figures and references, with the ability to search, customize your content, make notes and highlights, and have content read aloud Updated and new clinical cases, supported with photography by the not-for-profit organization, Positive Exposure New content on growing role of sequencing and novel functional assays in diagnosis and screening of genetic conditions New chapter on Epigenetics Clearer and more precise terminology, in response to contemporary and evolving guidelines New sections describing the use (and need for) genetic information from diverse populations, including unique indigenous and founder populations, for diagnosis and management.