Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging (Monographs in Human Genetics, Vol. 15) - kelloggchurch.org

May 15, 2007 · Fanconi Anemia: A Paradigmatic Disease for the Understanding of Cancer and Aging Monographs in Human Genetics, Vol. 15 Hardcover – May 15, 2007 by D. Schindler Editor, H. Hoehn Editor, M. Schmid Series Editor & 0 more. Fanconi anemia FA is a rare genetic disease discovered 80 years ago by Guido Fanconi, an eminent Swiss pediatrician. It is characterized by short stature, skeletal anomalies, increased incidence of solid tumors and leukemias, bone marrow failure and cellular sensitivity to DNA damaging agents. / Schroeder-Kurth, T. --Fanconi anemia: a disease with many faces / Dietrich, R., Velleuer, E. --Milestones in Fanconi anemia research / Digweed, M., Hoehn, H., Sperling K. --Fanconi anemia genes: structure, mutations, and genotype-phenotype correlations / Kalb, R. [and others] --Cancer in Fanconi anemia and Fanconi anemia genes in cancer. ISBN: 9783318014617 3318014613: OCLC Number: 728412385: Notes: Titel und Beschreibung vom Lieferanten 22.08.2007. Description: Online-Datei. Series Title. Fanconi anemia FA is an inherited human disorder clinically characterized by varying combinations of typical congenital anomalies, bone marrow failure, and cancer susceptibility. Cellular features include genomic and chromosomal instability and hypersensitivity to DNA-cross-linking agents.

Definition Fanconi anemia FA is a human inherited disorder clinically characterized by variable congenital anomalies, bone marrow failure and cancer susceptibility. Cellular features include genomic and chromosomal instability and hypersensitivity to DNA-crosslinking agents. Fanconi anemia FA is a recessive chromosomal instability syndrome that is clinically characterized by a wide variety of symptoms including growth retardation and developmental abnormalities such as malformed digits, absent radii, and microcephaly. Mar 10, 2017 · Fanconi anemia FA is an inherited human disorder clinically characterized by varying combinations of typical congenital anomalies, bone marrow failure, and cancer susceptibility. Cellular features include genomic and chromosomal instability, and hypersensitivity to. Jun 21, 2012 · Fanconi anemia FA is a rare inherited disease characterized by developmental defects, short stature, bone marrow failure, and a high risk of malignancies. FA is heterogeneous: 15 genetic subtypes have been distinguished so far.

disease for the understanding of cancer and aging, ” Mono-graphs in Human Genetics, vol. 15. Inactivating mutations in the corresponding genes underlie the recessive disease Fanconi anemia. Jul 31, 2009 · Fanconi anemia FA is a genetically and phenotypically heterogeneous recessive disorder characterized by diverse congenital malformations, progressive pancytopenia, and predisposition to both hematologic malignancies and solid tumors.

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