<?xml version="1.0" encoding="UTF-8"?>
<mods xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns="http://www.loc.gov/mods/v3" version="3.1" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
  <titleInfo>
    <title>The new clinical genetics</title>
  </titleInfo>
  <name type="personal">
    <namePart>Read, Andrew</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Donnai, Dian</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <originInfo>
    <place>
      <placeTerm type="text">Bloxham</placeTerm>
    </place>
    <publisher>SCION PUBLISHING LTD</publisher>
    <dateIssued>2007</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <physicalDescription>
    <extent>428 p.</extent>
  </physicalDescription>
  <tableOfContents>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 disease? 14. What can we do about genetic disease? Glossary</tableOfContents>
  <note type="statement of responsibility"> Edited By Andrew Read and  Dian Donnai </note>
  <subject>
    <topic>Medical Genetics   Genetics (non-medical)</topic>
  </subject>
  <classification authority="ddc">616.042 REA D</classification>
  <identifier type="isbn">9781904842316</identifier>
  <recordInfo/>
</mods>
