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Titlebook: Bone Marrow Failure; Gary M. Kupfer,Gregory H. Reaman,Franklin O. Smith Book 2018 Springer International Publishing AG, part of Springer N

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Literature and Visual Technologiess involved in Diamond-Blackfan anemia. The recent finding that several genes affecting ribosome biogenesis are somatically mutated in human tumors implies that understanding the molecular mechanisms underlying this rare group of disorders will likely have much broader implications.
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https://doi.org/10.1007/978-3-031-12330-6syndrome (.) gene. SBDS functions in ribosomal biogenesis as well as other cellular processes. In this chapter we will summarize clinical manifestations of SDS and diagnostic and treatment approaches, as well as highlight novel advances in the understanding of the molecular pathogenesis of SDS.
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Gertrude Stein’s Machinery of Perceptionand supportive care. Advances in gene discovery and genetic diagnostic techniques have shown that as many as 20–30% of patients previously thought to have idiopathic AA actually have an underlying genetic cause, making it clear that extending genetic testing beyond basic screening is of paramount im
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https://doi.org/10.1007/978-3-031-12330-6transplantation in severe aplastic anemia, Fanconi anemia, dyskeratosis congenita, Diamond-Blackfan anemia, Shwachman-Diamond syndrome, severe congenital neutropenia, and congenital amegakaryocytic thrombocytopenia. The forthcoming role of gene therapy is also discussed.
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Acquired Aplastic Anemia,and supportive care. Advances in gene discovery and genetic diagnostic techniques have shown that as many as 20–30% of patients previously thought to have idiopathic AA actually have an underlying genetic cause, making it clear that extending genetic testing beyond basic screening is of paramount im
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