At least 180,000 autochthonous and allochthonous people are carriers of a large spectrum of hemoglobinopathies in The Netherlands. We describe two cases, the first, a 33-year old Surinamese Creole woman, studied because of an intermediate hemolytic anemia; the second, a couple requesting analysis because of a previously diagnosed carrier state in the male partner, while the carrier state in the pregnant female was uncertain.
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Vol. 90 No. 4 (2005): April, 2005 : Case Reports
Ferrata Storti Foundation, Pavia, Italy
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How to Cite
PC Giordano, MJ Bouva, P Van Delft, N Akkerman, MC Kappers-Klunne, CL Harteveld. A new polyadenylation site mutation associated with a mild beta-thalassemia phenotype. Haematologica 2005;90(4):551-552; https://doi.org/10.3324/%x.