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  <titleInfo>
    <title>ISCN 1985</title>
    <subTitle>an international system for human cytogenetic nomenclature (1985) : report of the Standing Committee on Human Cytogenetic Nomenclature</subTitle>
  </titleInfo>
  <titleInfo type="uniform">
    <title>Cytogenetics and cell genetics</title>
  </titleInfo>
  <titleInfo type="alternative">
    <title>International system for human cytogenetic nomenclature (1985)</title>
  </titleInfo>
  <name type="corporate">
    <namePart>Standing Committee on Human Cytogenetic Nomenclature</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <name type="personal">
    <namePart>Harnden, D. G.</namePart>
  </name>
  <name type="personal">
    <namePart>Klinger, Harold P.</namePart>
    <namePart type="date">1929-</namePart>
  </name>
  <name type="corporate">
    <namePart>March of Dimes Birth Defects Foundation</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">sz</placeTerm>
    </place>
    <place>
      <placeTerm type="text">Basel</placeTerm>
    </place>
    <place>
      <placeTerm type="text">New York</placeTerm>
    </place>
    <publisher>S. Karger</publisher>
    <dateIssued>1985</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>vi, 117 p. : ill. ; 26 cm.</extent>
  </physicalDescription>
  <note type="statement of responsibility">scientific editors, David G. Harnden, Harold P. Klinger ; assistant editors, Joseph T. Jensen, Margot Kaelbling.</note>
  <note>Includes index.</note>
  <note>"Published in collaboration with the March of Dimes Birth Defects Foundation and Cytogenetics and cell genetics."--Verso t.p.</note>
  <note>Bibliography: ( p. 108-109).</note>
  <subject authority="lcsh">
    <topic>Human cytogenetics</topic>
    <topic>Nomenclature</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Human cytogenetics</topic>
    <topic>Terminology</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Human chromosome abnormalities</topic>
    <topic>Nomenclature</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Human chromosome abnormalities</topic>
    <topic>Terminology</topic>
  </subject>
  <classification authority="ddc">611.0181 INT</classification>
  <classification authority="nlm">QH 431 S785i (P)</classification>
  <identifier type="isbn">3805538707</identifier>
  <identifier type="lccn">85050076</identifier>
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    <recordCreationDate encoding="marc">861120</recordCreationDate>
    <recordChangeDate encoding="iso8601">20150123152023.0</recordChangeDate>
    <recordIdentifier source="BD-DhUL">428818</recordIdentifier>
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