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  <titleInfo>
    <title>Medical genetics</title>
  </titleInfo>
  <name type="personal">
    <namePart>Young, Ian D.</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <genre authority="local">Print books.</genre>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">enk</placeTerm>
    </place>
    <place>
      <placeTerm type="text">Oxford</placeTerm>
    </place>
    <place>
      <placeTerm type="text">New York</placeTerm>
    </place>
    <publisher>Oxford University Press</publisher>
    <dateIssued>2010</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>xi, 304 p. : ill. (some col.) ; 25 cm.</extent>
  </physicalDescription>
  <tableOfContents>Gene structure and function -- Chromosomes and cell division -- Common chromosome disorders -- Single-gene (Mendelian) inheritance -- Identifying genes for Mendelian diseases -- Polygenic inheritance and complex diseases -- Genes and populations -- Genes and haemoglobin -- Genes and development -- Genes and cancer -- Genes and biochemistry -- Genes, drugs, and treatment -- Clinical skills and scenarios -- Applied clinical genetics -- Appendix 1: Medical school core curriculum in genetics -- Appendix 2: Teaching medical genetics to undergraduate medical students -- Glossary.</tableOfContents>
  <note type="statement of responsibility">Ian D. Young.</note>
  <note>Originally published: 2005.</note>
  <note>Includes bibliographical references and index.</note>
  <subject authority="lcsh">
    <topic>Medical genetics</topic>
  </subject>
  <subject authority="mesh">
    <topic>Genetics, Medical</topic>
  </subject>
  <subject authority="mesh">
    <topic>Chromosome Aberrations</topic>
  </subject>
  <subject authority="mesh">
    <topic>Genetic Diseases, Inborn</topic>
  </subject>
  <classification authority="lcc">RB155 .Y68 2010</classification>
  <classification authority="ddc" edition="22">616.042</classification>
  <identifier type="isbn">0199594619 (pbk.)</identifier>
  <identifier type="isbn">9780199594610 (pbk.)</identifier>
  <identifier type="lccn">2011280131</identifier>
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    <recordCreationDate encoding="marc">110224</recordCreationDate>
    <recordChangeDate encoding="iso8601">20161026150907.0</recordChangeDate>
    <recordIdentifier source="US-DLC">16664688</recordIdentifier>
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