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  <titleInfo>
    <title>Management of genetic syndromes</title>
  </titleInfo>
  <name type="personal">
    <namePart>Cassidy, Suzanne B.</namePart>
  </name>
  <name type="personal">
    <namePart>Allanson, Judith E.</namePart>
  </name>
  <typeOfResource>text</typeOfResource>
  <genre authority="marc">bibliography</genre>
  <originInfo>
    <place>
      <placeTerm type="code" authority="marccountry">nju</placeTerm>
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    <place>
      <placeTerm type="text">Hoboken, N.J</placeTerm>
    </place>
    <publisher>Wiley-Liss</publisher>
    <dateIssued>c2005</dateIssued>
    <dateIssued encoding="marc">2005</dateIssued>
    <edition>2nd ed.</edition>
    <issuance>monographic</issuance>
  </originInfo>
  <language>
    <languageTerm authority="iso639-2b" type="code">eng</languageTerm>
  </language>
  <physicalDescription>
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    <extent>xvii, 695 p. : ill. ; 29 cm.</extent>
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  <tableOfContents>Aarskog syndrome / Roger E. Stevenson --  Achondroplasia / Richard M. Pauli -- Alagille syndrome / Binita M. Kamath and Ian Krantz -- Albinism / Richard A. King and C. Gail Summers -- Angelman syndrome / Charles A. Williams -- Arthrogryposis / Judith G. Hall -- ATR-X / Richard J. Gibbons -- Bardet-Biedl syndrome / Anne M. Slavotinek -- Beckwith-Wiedemann syndrome / Rosanna Weksberg and Cheryl Shuman -- CHARGE association / Christine A. Oley -- Coffin-Lowry syndrome / Alasdair G.W. Hunter -- Cornelia de Lange syndrome / David E. Fitzpatrick and Antonie D. Kline -- Costello syndrome / Angela E. Lin, Karen W. Gripp and Bronwyn Kerr --</tableOfContents>
  <tableOfContents>Craniosynostosis / Karen W. Gripp and Elaine H. Zackai -- Denys-Drash syndrome / Carol L. Clericuzio -- Down syndrome / Alasdair G.W. Hunter -- Ehlers-Danlos syndrome / Richard J. Wenstrup and Leah B. Hoechstetter -- Fetal alcohol syndrome / Albert E. Chudley and Sally E. Longstaffe -- Fetal anticonvulsants / Renata C. Gallagher, Kerry Kingham and H. Eugene Hoyme -- Fragile X syndrome / Randi J. Hagerman -- Gorlin syndrome (nevoid basal cell carcinoma syndrome) / Peter Farndon -- Hereditary haemorrhagic telangiectasia / Mary E.M. Porteous -- Holoprosencephaly / Andrea L. Gropman and Maximilian Muenke --</tableOfContents>
  <tableOfContents>Incontinetia pigmenti / Dian Donnai -- Kabuki syndrome / Louanne Hudgins -- Klinefelter syndrome / Joe Leigh Simpson ... [et al.] -- Marfan syndrome / Iris Schrijver, Deborah M. Alcorn and Uta Francke -- Myotonic dystrophy / Christine E.M. deDie Smulders, Frans G.I. Jennekens and Chris J. H"weler -- Neurofibromatosis type 1 / David Viskochil -- Noonan syndrome / Judith E. Allanson -- Oculo-auriculo-vertebral spectrum / Robert J. Gorlin -- Osteogenesis imperfecta / Joan C, Marin, Anne Letocha and Edith J. Chernoff -- Pallister-Hall and Greig cephalopolysyndactyly syndrome / Leslie G. Biesecker --</tableOfContents>
  <tableOfContents>Prader-Willi syndrome / Suzanne B. Cassidy -- Proteus syndrome / Leslie G. Biesecker -- Rett syndrome / Eric E. Smeets and Connie T.R.M. Schrander-Stumpel -- Robin sequence / Robert J. Shprintzen -- Rubinstein-Taybi syndrome / Raoul C.M. Hennekam -- Russell-Silver syndrome / Howard M. Saal -- Smith-Lemli-Opitz syndrome / Christopher Cunniff and Theresa A. Grebe -- Smith-Magenis syndrome / Ann C.M. Smith -- Sotos syndrome / Trevor R.P. Cole -- Stickler syndrome / Clair Francomano, Douglas J. Wilkin and Ruth M. Liberfarb --</tableOfContents>
  <tableOfContents>Terminal 22q- / Mary C. Phelan, Gail A. Stapleton and R. Curtis Rogers -- Treacher-Collins syndrome / Marilyn C. Jones -- Trisomy 13 and 18 syndromes / John C. Carey -- Tuberous sclerosis / John R.W. Yates -- Turner syndrome / Virginia P. Sybert -- VATER syndrome / Bryan D. Hall -- Velo-Cario-facial syndrome / Robert J. Shprintzen -- Von Hippel Lindau syndrome / R. Neil Schimke and Debra L. Collins -- WAGR syndrome / Carol L. Clericuzio -- Williams syndrome / Colleen A. Morris -- Wolf-Hirschhorn / Agatino Battaglia.</tableOfContents>
  <note type="statement of responsibility">edited by Suzanne B. Cassidy, Judith E. Allanson.</note>
  <note>Includes bibliographical references and index.</note>
  <subject authority="lcsh">
    <topic>Genetic disorders</topic>
  </subject>
  <subject authority="mesh">
    <topic>Genetic Diseases, Inborn</topic>
    <topic>diagnosis</topic>
  </subject>
  <subject authority="mesh">
    <topic>Abnormalities, Multiple</topic>
    <topic>diagnosis</topic>
  </subject>
  <subject authority="mesh">
    <topic>Abnormalities, Multiple</topic>
    <topic>therapy</topic>
  </subject>
  <subject authority="mesh">
    <topic>Genetic Diseases, Inborn</topic>
    <topic>therapy</topic>
  </subject>
  <classification authority="lcc">RB 155.5 .M36 2005</classification>
  <classification authority="nlm">QZ 50 M2655 2005</classification>
  <identifier type="isbn">978-0471308706 (cloth : alk. paper)</identifier>
  <identifier type="lccn">2004004693</identifier>
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