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	1.	Hb Zoetermeer: a new mutation on the alpha2 gene inducing an Ala-->Ser substitution at codon 21 is possibly associated with a mild thalassemic phenotype. [electronic resource] by 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 Producer: 20071005 In: Hemoglobin vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene. [electronic resource] by Harteveld, Cornelis L Oosterhuis, Wytze P Schoenmakers, Christian H H Ananta, Hardjawardhama Kos, Snjezana Bakker Verweij, Margaretha van Delft, Peter Arkesteijn, Sandra G J Phylipsen, Marion Giordano, Piero C Producer: 20100603 In: European journal of haematology vol. 84 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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