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	1.	Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different families. [electronic resource] by Stasia, Marie José van Leeuwen, Karin de Boer, Martin Martel, Cecile Mollin, Michele Thuret, Isabelle Michel, Gerard Hanson, Celine Augustine, Nancy H Coutton, Charles Satre, Véronique Wittwer, Carl T Hill, Harry Roos, Dirk Producer: 20130122 In: Journal of clinical immunology vol. 32 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Functional and genetic characterization of two extremely rare cases of Williams-Beuren syndrome associated with chronic granulomatous disease. [electronic resource] by Stasia, Marie J Mollin, Michèle Martel, Cécile Satre, Véronique Coutton, Charles Amblard, Florence Vieville, Gaëlle van Montfrans, Joris M Boelens, Jaap J Veenstra-Knol, Hermine E van Leeuwen, Karen de Boer, Martin Brion, Jean-Paul Roos, Dirk Producer: 20140501 In: European journal of human genetics : EJHG vol. 21 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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