Sandra G.J. Arkesteijn

Occurrence of common and rare δ‐globin gene defects in two multiethnic populations: thirteen new mutations and the significance of δ‐globin gene defects in β‐thalassemia diagnostics

Marion Phylipsen, Monica V.E. Gallivan, Sandra G.J. Arkesteijn et al. · International Journal of Laboratory Hematology · 2010 · 39 citations

Life Sciences, Genetics, Molecular Genetics +14

The First Case of Hb Groene Hart [α119(H2)Pro→Ser,<i>C</i>CT→<i>T</i>CT (α1)] Homozygosity Confirms That a Thalassemia Phenotype Is Associated with this Abnormal Hemoglobin Variant

Piero C. Giordano, Sonja Zweegman, Nicole Akkermans et al. · Hemoglobin · 2007 · 27 citations

Life Sciences, Genetics, Molecular Genetics +11

Hb Lepore-Leiden: A New δ/β Rearrangement Associated with a β-Thalassemia Minor Phenotype

Cornelis L. Harteveld, Pierre W. Wijermans, Sandra G.J. Arkesteijn et al. · Hemoglobin · 2008 · 24 citations

Medicine, Genetics, Hematology +17

Hb Haaglanden: a new nonsickling β7Glu&gt;Val variant. Consequences for basic diagnostics, screening, and risk assessment when dealing with HbS‐like variants

Cornelis L. Harteveld, G. A. E. Ponjee, Margreet Bakker‐Verweij et al. · International Journal of Laboratory Hematology · 2012 · 18 citations

Life Sciences, Genetics, Hematology +16

Two New α1-Globin Gene Point Mutations: Hb Nedlands (HBA1:c.86C&gt;T) [α28(B9)Ala→Val] and Hb Queens Park (HBA1:c.98T&gt;A) [α32(B13)Met→Lys]

Marion Phylipsen, John F. Prior, Erna Lim et al. · Hemoglobin · 2010 · 17 citations

Life Sciences, Genetics, Molecular Genetics +17