Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/49912
Title: Characterization of a newly discovered α-thalassaemia-1 in two Spanish patients with Hb H disease
Authors: Gonzalez-Redondo, J. M.
Diaz-Chico, J. C. 
Malcorra-Azpiazu, J. J.
Balda-Aguirre, M. I.
Huisman, T. H.J.
UNESCO Clasification: 32 Ciencias médicas
320102 Genética clínica
Issue Date: 1988
Journal: British journal of haematology (Print) 
Abstract: A new deletion of more than 27 kb, removing the Ψζ1, Ψα2, Ψα1, α2, α1 and θ1 globin genes has been found in four members of a Spanish family, including two patients with Hb H disease. The 5’end point of the deletion is located between the ζ and Ψζ genes, and the 3’end of the deletion is downstream of the 3’hypervariable region.
URI: http://hdl.handle.net/10553/49912
ISSN: 0007-1048
DOI: 10.1111/j.1365-2141.1988.tb02517.x
Source: British Journal of Haematology[ISSN 0007-1048],v. 70(4), p. 459-463 (Diciembre 1988)
Appears in Collections:Artículos
Show full item record

SCOPUSTM   
Citations

18
checked on Nov 27, 2022

Page view(s)

33
checked on Oct 29, 2022

Google ScholarTM

Check

Altmetric


Share



Export metadata



Items in accedaCRIS are protected by copyright, with all rights reserved, unless otherwise indicated.