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Chromosomal Breakage in Response to Cross-linking Agents in the Diagnosis of Fanconi Anemia

  • F. Arwert
  • M. L. Kwee

Abstract

The Fanconi anemia (FA) syndrome was originally described by Guido Fanconi in 1927. In his report he described three brothers with a condition resembling pernicious anemia. Evidently the anemia was the main symptom of the disease. Subsequently, other clinical symptoms (e.g., thumb aplasia and other skeletal abnormalities, café au lait spots, and growth retardation) frequently observed in FA have been described (Nilsson 1960; Fanconi 1967).

Keywords

Aplastic Anemia Fanconi Anemia Lymphocyte Culture Xeroderma Pigmentosum Ataxia Telangiectasia 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Copyright information

© Springer-Verlag Berlin Heidelberg 1989

Authors and Affiliations

  • F. Arwert
  • M. L. Kwee

There are no affiliations available

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