Fanconi anemia: A disease with many faces

Monographs in Human Genetics

Volumn 15, Issue , 2007, Pages 9-22

  Dietrich, R ^a   Velleuer, E ^b  

^a Deutsche Fanconi Anämie Hilfe EV ^*  (Germany)

^b UNIVERSITY HOSPITAL DÜSSELDORF   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84870178243     PISSN: 00770876     EISSN: 16623835     Source Type: Book Series    
DOI: 10.1159/000102545     Document Type: Article

References (7)

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2. Frohnmayer L, Frohnmeyer D: Fanconi Anemia. A Handbook for Families and Their Physicians. ed 3. Eugene, Oregon, Fanconi Anemia Research Fund Inc., 2000.
3. Fanconi Anämie. Ein Handbuch für Eltern, Patienten und ihre Ärzte. Translated version and extension of reference 2. Deutsche Fanconi-Anämie-Hilfe e. V., Unna, 2005.
4. Schoof E, Beck JD, Joenje H, Doerr HG: Growth hormone deficiency in one of two siblings with Fanconi's anemia complementation group FA-D. Growth Horm IGF Res 2000;10:290-294.
5. Metzger S, Bauer P, Tomiuk J, Laccone F, Didonato S, et al: The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington's disease. Neurogenetics 2006;7:27-30. (Pubitemid 43327681)
6. Kwee ML, Van der Kleij JM, Van Essen AJ, Begeer JH, Joenje H, et al: An atypical case of Fanconi anemia in elderly sibs. Am J Med Genet 1997;68:62-66.
7. Huck K, Hanenberg H, Gudowius S, Fenk R, Kalb R, et al: Delayed diagnosis and complications of Fanconi anemia at advanced age - a paradigm. Br J Haematol 2006;133:188-197.