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Fanconi Anemia : Clinical, Cytogenetic and Experimental Aspects

Author: Traute M Schroeder-Kurth; Arleen D Auerbach; G Obe
Publisher: Berlin, Heidelberg : Springer Berlin Heidelberg, 1989.
Edition/Format:   eBook : Document : EnglishView all editions and formats
Summary:
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  Read more...
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Genre/Form: Electronic books
Additional Physical Format: Print version:
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Traute M Schroeder-Kurth; Arleen D Auerbach; G Obe
ISBN: 9783642741791 3642741797
OCLC Number: 851782555
Description: 1 online resource (xx, 264 pages 69 illustrations)
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.
Responsibility: edited by Traute M. Schroeder-Kurth, Arleen D. Auerbach, Günter Obe.

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.

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