Molecular analysis of complex cases of alpha- and beta-thalassemia in Mexican mestizo patients with microcytosis and hypochromia reveals two novel alpha(0)-thalassemia deletions --(Mex1) and --(Mex2)

Author(s):
De-La-Cruz-Salcedo, E.I.; Ibarra, B.; Rizo-De-La-Torre, L.C.; Sanchez-Lopez, J.Y.; Gonzalez-Mercado, A.; Harteveld, C.L.; Perea-Diaz, F.J.
Published
2016
Publication type
Article / Letter to editor
complex - and -thalassemia genotypesmicrocytosisalpha-globin deletion
Date issued
2016-10-31
Language
English
Is part of
International Journal of Laboratory Hematology (2016), Vol. 38, no. 5, p. 535-542
hdl
1887/113312
doi
10.1111/ijlh.12536