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Fanconi Anemia
. Ed(S): Schroeder-Kurth, T.M.; Auerbach, Arleen D.; Obe, Gunter
€ 128.07
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Description for Fanconi Anemia
Paperback. Editor(s): Schroeder-Kurth, T.M.; Auerbach, Arleen D.; Obe, Gunter. Num Pages: 264 pages, biography. BIC Classification: MFN; MJCL; MJF; MJT. Category: (P) Professional & Vocational. Dimension: 244 x 170 x 15. Weight in Grams: 501.
Sixty years ago, G. Fanconi published a paper entitled: "Familiiire infantile pemiziosaartige Aniimie (pemizioses Blutbild und Konstitu- tion)", in which he reported that this type of severe aplastic anemia represents a hereditary disease distinct from other pancytopenias of childhood (Fanconi 1927). Later this syndrome was named Fan- coni anemia (FA; van Leeuwen 1933). A more recent study of the genetics of FA confirmed that the syndrome is inherited in an au- tosomal recessive manner (Schroeder et al. 1976). Prenatal diagno- sis in FA families showed that about 25% of fetuses are affected (Auerbach et al. 1985, 1986). In 1964, Schroeder ... Read more
Sixty years ago, G. Fanconi published a paper entitled: "Familiiire infantile pemiziosaartige Aniimie (pemizioses Blutbild und Konstitu- tion)", in which he reported that this type of severe aplastic anemia represents a hereditary disease distinct from other pancytopenias of childhood (Fanconi 1927). Later this syndrome was named Fan- coni anemia (FA; van Leeuwen 1933). A more recent study of the genetics of FA confirmed that the syndrome is inherited in an au- tosomal recessive manner (Schroeder et al. 1976). Prenatal diagno- sis in FA families showed that about 25% of fetuses are affected (Auerbach et al. 1985, 1986). In 1964, Schroeder ... Read more
Product Details
Format
Paperback
Publication date
2011
Publisher
Springer-Verlag Berlin and Heidelberg GmbH & Co. KG Germany
Number of pages
264
Condition
New
Number of Pages
264
Place of Publication
Berlin, Germany
ISBN
9783642741814
SKU
V9783642741814
Shipping Time
Usually ships in 15 to 20 working days
Ref
99-15
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