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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.	A new alpha(0)-thalassemia deletion found in a Dutch family (--(AW)). [electronic resource] by 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 Producer: 20101207 In: Blood cells, molecules & diseases vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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