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	1.	Clinical relevance of point mutations in the cytoplasmic domain of the granulocyte colony-stimulating factor receptor gene in patients with severe congenital neutropenia. [electronic resource] by Tidow, N Pilz, C Teichmann, B Müller-Brechlin, A Germeshausen, M Kasper, B Rauprich, P Sykora, K W Welte, K Producer: 19970422 In: Blood vol. 89 Availability: No items available. Save to lists Add to cart (remove)
	2.	No evidence for a major role of heterozygous deletion 657del5 within the NBS1 gene in the pathogenesis of non-Hodgkin's lymphoma of childhood and adolescence. [electronic resource] by Stanulla, M Stümm, M Dieckvoss, B O Seidemann, K Schemmel, V Müller Brechlin, A Schrappe, M Welte, K Reiter, A Producer: 20000712 In: British journal of haematology vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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