Genetics in Medicine, 9780198841555
Paperback
Unlock the secrets of heredity, disease, and personalized medicine’s future.

$100.94

  • Paperback

    160 pages

  • Release Date

    6 July 2020

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Summary

Unlocking the Code: Genetics in Medicine for the Next Generation

Written primarily for students embarking on an undergraduate bioscience degree, this primer reviews the essential biological concepts that underpin any programme of more advanced study. It offers early-stage undergraduates the opportunity to review topics about which they may feel under-prepared or less confident.

Genetic medicine has entered an era of rapid expansion. It is no longer just relevant to families …

Book Details

ISBN-13:9780198841555
ISBN-10:0198841558
Series:Oxford Biology Primers
Author:Barbara Jennings, Gavin Willis, Nandu Thalange
Publisher:Oxford University Press
Imprint:Oxford University Press
Format:Paperback
Number of Pages:160
Release Date:6 July 2020
Weight:332g
Dimensions:247mm x 190mm x 10mm
About The Author

Barbara Jennings

Barbara Jennings was part of the faculty team that established Norwich Medical School at UEA. She is a senior lecturer and the academic lead for their genetics curriculum. Barbara is a scientist with a PhD about cancer genetics from UEA (1995), and a background in clinical molecular diagnostics for the NHS. Her published research spans cancer genetics, genetic epidemiology, and pharmacogenetics. Barbara is also the course director of a free online course about pharmacogenetics.

Nandu Thalange graduated from King’s College, London in 1988, intent on a career in paediatric endocrinology. During training, Nandu was exposed to a large number of genetic disorders with implications for the endocrinologist which stimulated his interest in this area. For many years he was a senior lecturer at UEA and taught genetics to medical students from the inception of the Norwich Medical School. He remains active as a teacher and clinician and was recently appointed as an honorary Professor of Paediatrics at Mohammed Bin Rashid University, Dubai.

Gavin Willis graduated from Imperial College, London in 1985, and began his career in molecular biology and human genetics. He completed his PhD at the John Innes Institute in Norwich, and joined the pathology department at the Norfolk and Norwich University Hospital in 1996, to develop molecular diagnostic markers for leukaemia. Gavin is the principal clinical scientist in the section of molecular genetics, and a specialist in the genetic tests used for the management of families affected by hereditary haemochromatosis.

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