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: Fanconi Anemia
    sub title: Clinical, Cytogenetic and Experimental Aspects
  name:
    name part: Schroeder-Kurth, Traute M.
    role:
      role term: creator
  name:
    name part: Auerbach, Arleen D.
  name:
    name part: Obe, G.
  name:
    name part: SpringerLink (Online service)
  type of resource: text
  genre: Electronic books.
  origin info:
    place:
      place term: gw
    date issued: 1989
    issuance: monographic
  language:
    language term: eng
  physical description:
    reformatting quality: access
    form: remote
    extent: 1 online resource (xx, 264 pages 69 illustrations)
  abstract: This monograph represents the first attempt to gather all aspects of Fanconi's anemia in one source. The editors are well-known for their continuous research in the field and have aptly brought together contributions containing the most up-to-date information available. The difficulties in differential diagnosis and treatment are covered; and the outlook for cure via bone marrow transplantation is included. This overview will interest specialists in human genetics as well as all those dealing with this disease.
  table of contents: Clinical and Therapeutical Aspects: International Fanconi Anemia Registry: First Report. Fanconi Anemia in The Netherlands. Clinical Aspects of a Cluster of 42 Patients in South Africa with Fanconi Anemia. Therapeutic Aspects of Fanconi Anemia. Bone Marrow Transplantation for Fanconi Anemia -- Spontaneous and Induced Chromosomal Breakage for Diagnosis of Patients with Fanconi Anemia and Their Relatives: Diepoxybutane Test for Prenatal and Postnatal Diagnosis of Fanconi Anemia. Chromosomal Breakage in Response to Crosslinking Agents in the Diagnosis of Fanconi Anemia. Cytogenetic Studies in Fanconi Anemia: Induced Chromosomal Breakage and Cytogenetics of Leukemia. Aplastic Anemia and Fanconi Anemia: Response of Lymphocytes to X-Rays and Mitomycin C. Variation in Cellular Sensitivities Among Fanconi Anemia Patients, Non-Fanconi Anemia-Patients, Their Parents and Siblings, and Control Probands. Significance of Cellular Sensitivity in a Group of Parents of Fanconi Anemia Patients. Chromosomal Studies in Fanconi Anemia Heterozygotes -- Investigations of the Defect in Fanconi Anemia Cells: BrdU-Hoechst Flow Cytometry Links the Cell Kinetic Defect of Fanconi Anemia to Oxygen Hypersensitivity. Oxygen Metabolism and Chromosomal Breakage in Fanconi Anemia. Cellular Effects of Fanconi Anemia Genes and Their Correction by Microinjection. Phenotypic and Genetic Heterogeneity in Fanconi Anemia, Fate of Cross-Links, and Correction of the Defect by DNA Transfection -- Complementation Studies in Fanconi Anemia: Complementation Studies in Fanconi Anemia. Complementation and Gene Transfer Studies in Fanconi Anemia. Complementation Studies in Fanconi Anemia Using Cell Fusion and Microinjection of mRNA -- Fanconi Anemia: The Family's Point of View -- Subject Index.
  note: edited by Traute M. Schroeder-Kurth, Arleen D. Auerbach, Günter Obe.
  note: Electronic resource.
  subject:
    topic: Medicine
  subject:
    topic: Human genetics
  subject:
    topic: Obstetrics
  subject:
    topic: Hematology
  subject:
    topic: Oncology
  subject:
    topic: Hematology
  subject:
    topic: Human genetics
  subject:
    topic: Medicine
  subject:
    topic: Obstetrics
  subject:
    topic: Oncology
  classification: RB155-155.8
  classification: QH431
  classification: 611.01816
  classification: 599.935
  identifier: 9783642741791 (electronic bk.)
  identifier: 3642741797 (electronic bk.)
  identifier: 9783642741814
  identifier: 3642741819
  identifier: http://proxy.library.tamu.edu/login
  record info:
    record content source: AU@
    record creation date: 121227
    record change date: 20260422224648.9
    record identifier: in00003568799
    language of cataloging:
      language term: eng