rdf-syntax-grammar
mods:
  schema location: http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-2.xsd
  title info:
    title: Muscular dystrophy
    sub title: methods and protocols
  name:
    name part: Bushby, Katherine.
  name:
    name part: Anderson, Louise V. B.
  type of resource: text
  genre: bibliography
  origin info:
    place:
      place term: nju
    date issued: 2001
    issuance: monographic
  language:
    language term: eng
  physical description:
    form: print
    extent: xii, 457 pages : illustrations
  table of contents: Application of molecular methodologies in muscular dystrophies / K.M.D. Bushby ... [et al.] -- Clinical examination as a tool for diagnosis : historical perspective / D. Gardner-Medwin -- Histopathological diagnosis of muscular dystrophies / M.A. Johnson -- Serum creatine kinase in progressive muscular dystrophies / M. Zatz ... [et al.] -- Deletion and duplication analysis in males affected with Duchenne or Becker muscular dystrophy / A. Curtis ... [et al.] -- Point mutation detection in the dystrophin gene / J.T. den Dunnen -- DNA-based techniques for detection of carriers of Duchenne and Becker muscular dystrophy / E. Bakker -- Fluorescence in situ hybridization analysis for carrier detection in Duchenne/Becker muscular dystrophy / J.K. Dore ... [et al.] -- DNA-based prenatal diagnosis for Duchenne and Becker muscular dystrophy / A. Curtis ... [et al.] -- Molecular diagnosis and genetic counseling of the manifesting carrier of Duchenne muscular dystrophy / E.P. Hoffman ... [et al.] -- Mutation analysis of X-linked Emery-Dreifuss muscular dystrophy gene / D. Toniolo -- Analysis of the LAMA2 gene in merosin-deficient congenital dystrophy / A. Helbling-Leclerc ... [et al.] -- Alpha-carcoglycan mutations / F. Piccolo ... [et al.] -- Mutation detection in beta- and gamma-sarcoglycan (LGMD2E and LGMD2C) / C.G. Bönnemann ... [et al.] -- Mutation analysis in delta-sarcoglycan (LGMD2F) / V. Nigro -- Molecular diagnosis of calpainopathies : methods used for detection of mutations in CAPN3 gene implicated in limb-girdle muscular dystrophy type 2A / I. Richard ... [et al.] -- Molecular investigation of LGMD2B-haplotype analysis and mutation screening / R. Bashir ... [et al.] -- Molecular analysis of facioscapulohumeral muscular dystrophy (FSHD1) / S.M. van der Maarel ... [et al.] -- Analysis of protein expression in muscular dystrophies / L.V.B. Anderson -- Immunological reagents and amplification systems / C.A. Sewry ... [et al.] -- Immunocytochemical analysis / M.A. Johnson…
  note: edited by Katherine M.D. Bushby and Louise V.B. Anderson.
  note: Includes bibliographical references and index.
  subject:
    topic: Muscular Dystrophies
    topic: genetics
  subject:
    topic: Genetic Testing
  subject:
    topic: Molecular Biology
  subject:
    topic: Muscular Dystrophies
    topic: diagnosis
  classification: RC935.M7 M87 2001
  classification: 616.7
  classification: 2001 I-384
  classification: WE 559 M9853 2001
  related item:
    title info:
      title: Methods in molecular medicine ; 43
  identifier: 0896036952 (alk. paper)
  identifier: 00053902
  record info:
    record content source: NLM
    record creation date: 001020
    record change date: 20191203081959.0
    record identifier: in00004493470