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  <titleInfo>
    <title>Medical genetics</title>
    <subTitle>its application to speech, hearing, and craniofacial disorders</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Robin, Nathaniel.</namePart>
    <role>
      <roleTerm authority="marcrelator" type="text">creator</roleTerm>
    </role>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">cau</placeTerm>
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    <place>
      <placeTerm type="text">San Diego</placeTerm>
    </place>
    <publisher>Plural Pub.</publisher>
    <dateIssued>c2008</dateIssued>
    <dateIssued encoding="marc">2008</dateIssued>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
    <form authority="marcform">print</form>
    <extent>xii, 182 p. : ill. (chiefly col.) ; 26 cm.</extent>
  </physicalDescription>
  <tableOfContents>Genetics professionals: an overview / Nathaniel Robin -- Genetic inheritance: Mendelian, non-Mendelian and multi-factorial / Nathaniel H. Robin -- Evaluation of the patient with a congenital anomaly / Nathaniel H. Robin -- Classification of birth defects / Nathaniel H. Robin and Marni Falk -- Genetic testing: cytogenetics, biochemical genetics and molecular genetics / Nathaniel H. Robin and Edward J. Lose -- Ethical issues in genetic testing / Nathaniel H. Robin -- Genetic counseling and your practice / Nathaniel H. Robin and Sandra Prucka -- Genetics and hearing loss / Nathaniel H. Robin -- Craniofacial genetics I: cleft lip and cleft palate / Nathaniel H. Robin -- Craniofacial genetics II: craniosynostosis and related syndromes / Nathaniel H. Robin.</tableOfContents>
  <note type="statement of responsibility">Nathaniel H. Robin.</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>Genetic Diseases, Inborn</topic>
  </subject>
  <subject authority="mesh">
    <topic>Genetic Screening</topic>
  </subject>
  <classification authority="lcc">RB155 .R656 2008</classification>
  <classification authority="ddc" edition="22">616.042 ROB</classification>
  <relatedItem type="series">
    <titleInfo>
      <title>Genetic syndromes and communication disorders series</title>
    </titleInfo>
  </relatedItem>
  <identifier type="isbn">9781597562584 (pbk.)</identifier>
  <identifier type="isbn">1597562580 (pbk.)</identifier>
  <identifier type="lccn">2007036511</identifier>
  <identifier type="uri">http://www.loc.gov/catdir/toc/ecip0726/2007036511.html</identifier>
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    <url displayLabel="Table of contents only">http://www.loc.gov/catdir/toc/ecip0726/2007036511.html</url>
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    <recordCreationDate encoding="marc">070904</recordCreationDate>
    <recordChangeDate encoding="iso8601">20200226162324.0</recordChangeDate>
    <recordIdentifier source="OSt">14997294</recordIdentifier>
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