A new alpha(0)-thalassemia deletion found in a Dutch family (--(AW)) von Phylipsen, Marion, Vogelaar, Ingrid P, Schaap, Rianne A C, Arkesteijn, Sandra G J, Boxma, George L, van Helden, Willem C H, Wildschut, Irene C M, de Bruin-Roest, Andrea C, Giordano, Piero C, Harteveld, Cornelis L

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A new α0-thalassemia deletion found in a Dutch family (--AW) von Phylipsen, Marion, Vogelaar, Ingrid P., Schaap, Rianne A.C., Arkesteijn, Sandra G.J., Boxma, George L., van Helden, Willem C.H., Wildschut, Irene C.M., de Bruin-Roest, Andrea C., Giordano, Piero C., Harteveld, Cornelis L.

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A new α 0-thalassemia deletion found in a Dutch family (-- AW) von Phylipsen, Marion, Vogelaar, Ingrid P., Schaap, Rianne A.C., Arkesteijn, Sandra G.J., Boxma, George L., van Helden, Willem C.H., Wildschut, Irene C.M., de Bruin-Roest, Andrea C., Giordano, Piero C., Harteveld, Cornelis L.

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Hb Zoetermeer: A New Mutation on the α2 Gene Inducing an Ala→Ser Substitution at Codon 21 is Possibly Associated with a Mild Thalassemic Phenotype von Harteveld, Cornelis L., van Helden, Willem C.H., Boxma, George L., van Delft, Peter, Bakker-Verweij, Margaretha, Wajcman, Henri, Zanella-Cleon, Isabelle, Becchi, Michel, Giordano, Piero C.

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Hb 'T LANGE LAND [β136(H14)Gly → Arg]: A NEW HEMOGLOBIN VARIANT DESCRIBED IN A DUTCH PATIENT OF CHINESE ORIGIN von Harteveld, Cornelis, Plug, Robert J., Van Delft, Peter, Van Helden, Willem C. H., Giordano, Piero C.

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