References
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- Giordano PC, Harteveld CL, Bernini LF, et al. Haplotype analysis of two new, independent cases of Hb Osu-Christiansborg. Hemoglobin. 1999;23(2):193–195.
- Harteveld CL, van Delft P, Plug R, et al. Hb Groene Hart: a new Pro→Ser amino acid substitution at position 119 of the α1-globin chain is associated with a mild α-thalassemia phenotype. Hemoglobin. 2002;26(3):255–260.
- Harteveld CL, Wijermans PW, de Ree JE, et al. A new Hb Evanston allele [α14(A12)Trp → Arg] found solely, and in the presence of common α-thalassemia deletions, in three independent Asian cases. Hemoglobin. 2004;28(1):1–5.
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- Harteveld CL, Versteegh FG, Kok PJ, et al. Hb Bleuland [α108(G15)Thr→Asn, ACC→AAC (α2)]: a new abnormal hemoglobin associated with a mild α-thalassemia phenotype. Hemoglobin. 2006;30(3):349–354.
- Giordano PC, Plancke A, Van Meir CA, et al. Carrier diagnostics and prevention of hemoglobinopathies in early pregnancy in The Netherlands: a pilot study. Prenat Diagn. 2006;26(8):719–724.