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    Thompson & Thompson Genetics and Genomics in Medicine

    Thompson & Thompson Genetics and Genomics in Medicine by Cohn, Ronald; Scherer, Stephen; Hamosh, Ada;

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      • Publisher's listprice EUR 58.99
      • The price is estimated because at the time of ordering we do not know what conversion rates will apply to HUF / product currency when the book arrives. In case HUF is weaker, the price increases slightly, in case HUF is stronger, the price goes lower slightly.

        25 023 Ft (23 831 Ft + 5% VAT)
      • Discount 13% (cc. 3 253 Ft off)
      • Discounted price 21 770 Ft (20 733 Ft + 5% VAT)

    25 023 Ft

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    Availability

    Estimated delivery time: In stock at the publisher, but not at Prospero's office. Delivery time approx. 3-5 weeks.
    Not in stock at Prospero.

    Why don't you give exact delivery time?

    Delivery time is estimated on our previous experiences. We give estimations only, because we order from outside Hungary, and the delivery time mainly depends on how quickly the publisher supplies the book. Faster or slower deliveries both happen, but we do our best to supply as quickly as possible.

    Product details:

    • Edition number 9
    • Publisher Elsevier
    • Date of Publication 19 September 2023

    • ISBN 9780323547628
    • Binding Paperback
    • No. of pages580 pages
    • Size 276x215 mm
    • Weight 1440 g
    • Language English
    • Illustrations 543 illustrations (543 in full color)
    • 747

    Categories

    Long description:

    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 examination
    • 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.

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    Table of Contents:

    CHAPTER 1 Introduction
    CHAPTER 2 Introduction to the Human Genome
    CHAPTER 3 The Human Genome: Gene Structure and Function
    CHAPTER 4 Human Genetic Diversity: Genomic Variation
    CHAPTER 5 Principles of Clinical Cytogenetics and Genome Analysis
    CHAPTER 6 The Chromosomal and Genomic Basis of Disease: Disorders of the Autosomes and Sex Chromosomes
    CHAPTER 7 Patterns of Single-Gene Inheritance
    CHAPTER 8 Principles of Clinical Epigenetics
    CHAPTER 9 Complex Inheritance of Common Multifactorial Disorders
    CHAPTER 10 Population Genetics for Genomic Medicine
    CHAPTER 11 Identifying the Genetic Basis for Human Disease
    CHAPTER 12 The Molecular Basis of Genetic Disease
    CHAPTER 13 The Molecular, Biochemical, and Cellular Basis of Genetic Disease
    CHAPTER 14 The Treatment of Genetic Disease
    CHAPTER 15 Developmental Genetics and Birth Defects
    CHAPTER 16 Cancer Genetics and Genomics
    CHAPTER 17 Genetic Counseling and Risk Assessment
    CHAPTER 18 Preconception and Prenatal Screening and Diagnosis
    CHAPTER 19 Application of Genomics to Medicine and Individualized Health Care
    CHAPTER 20 Ethical and Social Issues in Genetics and Genomics
    Clinical Case Studies Illustrating Genetic Principles
    Glossary
    Answers to Problems
    Index

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    Thompson & Thompson Genetics and Genomics in Medicine

    Thompson & Thompson Genetics and Genomics in Medicine

    Cohn, Ronald; Scherer, Stephen; Hamosh, Ada; (ed.)

    25 023 HUF

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