|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|
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