A female with dyskeratosis congenita

dc.contributor.author	Amarasena, S.
dc.contributor.author	Hapuarachchi, G. K.
dc.contributor.author	De Silva, M. H. A. D.
dc.date.accessioned	2023-05-31T03:44:09Z
dc.date.available	2023-05-31T03:44:09Z
dc.date.issued	2005-09
dc.identifier.uri	http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/12890
dc.description.abstract	Dyskeratosis congenita is an inherited bone marrow failure syndrome, with multisystem involvement. Incidence is approximately 1 case per million population. 225 individuals have been reported in the literature1.	en_US
dc.language.iso	en	en_US
dc.publisher	Faculty of Medicine, University of Ruhuna, Galle, Sri Lanka	en_US
dc.subject	Dyskeratosis congenita	en_US
dc.subject	Child	en_US
dc.title	A female with dyskeratosis congenita	en_US
dc.type	Article	en_US