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	1.	A novel nonsense mutation of the mineralocorticoid receptor gene in a Swedish family with pseudohypoaldosteronism type I (PHA1). [electronic resource] by Nyström, A-M Bondeson, M-L Skanke, N Mårtensson, J Strömberg, B Gustafsson, J Annerén, G Producer: 20040211 In: The Journal of clinical endocrinology and metabolism vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Noonan syndrome and neurofibromatosis type I in a family with a novel mutation in NF1. [electronic resource] by Nyström, A M Ekvall, S Allanson, J Edeby, C Elinder, M Holmström, G Bondeson, M L Annerén, G Producer: 20100217 In: Clinical genetics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Noonan and cardio-facio-cutaneous syndromes: two clinically and genetically overlapping disorders. [electronic resource] by Nyström, A-M Ekvall, S Berglund, E Björkqvist, M Braathen, G Duchen, K Enell, H Holmberg, E Holmlund, U Olsson-Engman, M Annerén, G Bondeson, M-L Producer: 20080919 In: Journal of medical genetics vol. 45 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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