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  • New Clinical Genetics, third edition

    New Clinical Genetics, third edition by Read, Andrew; Donnai, Dian;

      • Kiadói listaár GBP 35.99
      • Az ár azért becsült, mert a rendelés pillanatában nem lehet pontosan tudni, hogy a beérkezéskor milyen lesz a forint árfolyama az adott termék eredeti devizájához képest. Ha a forint romlana, kissé többet, ha javulna, kissé kevesebbet kell majd fizetnie.

        17 194 Ft (16 375 Ft + 5% áfa)

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    Why don't you give exact delivery time?

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    A termék adatai:

    • Kiadás sorszáma 3
    • Kiadó Scion Publishing
    • Megjelenés dátuma 2015. június 8.

    • ISBN 9781907904677
    • Kötéstípus Puhakötés
    • Terjedelem472 oldal
    • Méret 268x208x19 mm
    • Nyelv angol
    • Illusztrációk 250
    • 0

    Kategóriák

    Rövid leírás:

    This new, updated edition of New Clinical Genetics continues to offer
    the most innovative case-based approach to modern genetics. It is used
    worldwide as a textbook for medical students, and is also an essential guide for genetic counselors and clinical and nurse
    geneticists.

    Több

    Hosszú leírás:

    HIGHLY COMMENDED IN THE 2016 BMA MEDICAL BOOK AWARDS!


    Instructors? comments on new, 3rd edition:


    "I LOVED the book.  I've never seen anything like it,
    and I've reviewed a lot of genetics texts. The way that cases are presented
    throughout is extremely novel."

    "I am greatly pleased with the revisions.  In my
    opinion, there is an increased clarity in the text (which will serve students
    well), and many welcomed updates based on current literature. Good job!"


    "I LIKE IT A LOT!!"

    "The book looks good and we will certainly be recommending
    it for our medical genetics course this autumn."


    "This is a fantastic book that I enjoy so much teaching
    from."

    "I have been reviewing the book.  I think it is a great
    teaching tool since you can follow a case from beginning to end."


    "I have used this book every year since the first edition
    was published and it is a perfect fit for my human genetics course.  I
    will definitely continue to use it."

    "It?s great. I will recommend the book as a main text for
    the medical student class."


    In the few years since
    the previous edition technical progress, especially the widespread use of
    whole-genome technologies, has brought many advances in the understanding,
    diagnosis and treatment of genetic disease. As a result, most chapters have
    been substantially rewritten and updated to reflect this. The unique structure
    and format remains the same, but significant new material has been added to
    cover:



    • the widespread use of next-generation sequencing as a routine diagnostic tool

    • the checking of a patient?s whole exome for the cause of their problem

    • noninvasive prenatal diagnosis by next-generation sequencing of free fetal DNA in the maternal circulation

    • a new integrated treatment of epigenetics

    • mosaicism, ?RASopathies? and disorders of the spliceosome are described in new Disease boxes

    • dysmorphology in more detail



    New Clinical Genetics continues to offer
    the most innovative case-based approach to modern genetics. It is used
    worldwide as a textbook for medical students, but also as an essential guide to
    the field for genetic counselors, physician assistants, and clinical and nurse
    geneticists.



    Reviews of earlier editions:



    ?This book provides a
    wonderful case-based learning environment. There are also self-assessment
    questions. Students are not given model answers but are provided with guidance
    on how to work out the correct answers for themselves. Excellent!?

    Human Genetics



    ?This book is a very valuable tool that will be
    used by future geneticists all over Europe and beyond, both as a teaching
    material and as a source of excellent knowledge.?

    European Journal of Human
    Genetics



    Több

    Tartalomjegyzék:

    1. What can
    we learn from a family history?

    2. How
    can a patient's chromosomes be studied?

    3. How do genes work?

    4. How can
    a patient's DNA be studied?

    5. How can
    we check a patient's DNA for gene mutations?

    6. What do mutations do?

    7. What
    is epigenetics?

    8. How do genes affect
    our metabolism, drug responses and immune system?

    9. How do researchers identify genes for
    mendelian diseases?

    10. Why are some conditions
    common and others rare?

    11. When is
    screening useful?

    12. Is cancer
    genetic?

    13. Should we be testing for
    genetic susceptibility to common diseases?

    14. What clinical services are available for families with genetic disorders?

    Guidance for self-assessment questions

    Glossary

    Index



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