Mobilizing Mutations

This book PDF is perfect for those who love Medical genre, written by Daniel Navon and published by University of Chicago Press which was released on 20 September 2019 with total hardcover pages 409. You could read this book directly on your devices with pdf, epub and kindle format, check detail and related Mobilizing Mutations books below.

Mobilizing Mutations
Author : Daniel Navon
File Size : 51,9 Mb
Publisher : University of Chicago Press
Language : English
Release Date : 20 September 2019
ISBN : 9780226638096
Pages : 409 pages
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Mobilizing Mutations by Daniel Navon Book PDF Summary

With every passing year, more and more people learn that they or their young or unborn child carries a genetic mutation. But what does this mean for the way we understand a person? Today, genetic mutations are being used to diagnose novel conditions like the XYY, Fragile X, NGLY1 mutation, and 22q11.2 Deletion syndromes, carving out rich new categories of human disease and difference. Daniel Navon calls this form of categorization “genomic designation,” and in Mobilizing Mutations he shows how mutations, and the social factors that surround them, are reshaping human classification. Drawing on a wealth of fieldwork and historical material, Navon presents a sociological account of the ways genetic mutations have been mobilized and transformed in the sixty years since it became possible to see abnormal human genomes, providing a new vista onto the myriad ways contemporary genetic testing can transform people’s lives. Taking us inside these shifting worlds of research and advocacy over the last half century, Navon reveals the ways in which knowledge about genetic mutations can redefine what it means to be ill, different, and ultimately, human.

Mobilizing Mutations

With every passing year, more and more people learn that they or their young or unborn child carries a genetic mutation. But what does this mean for the way we understand a person? Today, genetic mutations are being used to diagnose novel conditions like the XYY, Fragile X, NGLY1 mutation,

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