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  <titleInfo>
    <title>Mental retardation and developmental delay</title>
    <subTitle>genetic and epigenetic factors</subTitle>
  </titleInfo>
  <name type="personal">
    <namePart>Smith, Moyra.</namePart>
    <role>
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  <name type="personal">
    <namePart>Arfin, Stuart M.</namePart>
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  <name type="personal">
    <namePart>Lott, Ira T.</namePart>
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    <place>
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    <publisher>Oxford University Press</publisher>
    <dateIssued>2006</dateIssued>
    <issuance>monographic</issuance>
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    <extent>xix, 317 p. : ill. ; 25 cm.</extent>
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  <tableOfContents>Science, society, and mental retardation: a history -- Neurogenesis, neuronal migration, maturation, and function: insights into learning and memory -- Structural brain anomalies and neural tube defects -- Mental retardation associated with dysmorphology, growth retardation, or overgrowth -- Mental retardation associated with other neurological defects -- Mental retardation that develops after a period of normal cognition -- Non-syndromic mental retardation, autism, and language deficits -- Genomics, functional genomics, and epigenetics -- Establishing a diagnosis and determining etiology -- The value of genetic diagnosis: applying knowledge about etiology to prevention and treatment -- Epilogue: The value of genetic diagnosis--Applying knowledge about etiology to prevention and treatment.</tableOfContents>
  <note type="statement of responsibility">Moyra Smith.</note>
  <note>Includes bibliographical references (p. 247-300) and index.</note>
  <subject authority="lcsh">
    <topic>Mental retardation</topic>
    <topic>Etiology</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Mental retardation</topic>
    <topic>Genetic aspects</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Developmental disabilities</topic>
    <topic>Etiology</topic>
  </subject>
  <subject authority="lcsh">
    <topic>Developmental disabilities</topic>
    <topic>Genetic aspects</topic>
  </subject>
  <subject authority="mesh">
    <topic>Mental Retardation</topic>
    <topic>genetics</topic>
  </subject>
  <subject authority="mesh">
    <topic>Child</topic>
  </subject>
  <subject authority="mesh">
    <topic>Developmental Disabilities</topic>
    <topic>etiology</topic>
  </subject>
  <subject authority="mesh">
    <topic>Developmental Disabilities</topic>
    <topic>genetics</topic>
  </subject>
  <subject authority="mesh">
    <topic>Infant</topic>
  </subject>
  <subject authority="mesh">
    <topic>Mental Retardation</topic>
    <topic>etiology</topic>
  </subject>
  <classification authority="lcc">RC570 .S64 2006</classification>
  <classification authority="ddc" edition="22">616.858 804 2 SMI</classification>
  <classification authority="nlm">2005 O-500</classification>
  <classification authority="nlm">WS 107.5.B4 S655m 2006</classification>
  <identifier type="isbn">9780195174328 (alk. paper)</identifier>
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