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	1.	22q13 deletion syndrome. [electronic resource] by Phelan, M C Rogers, R C Saul, R A Stapleton, G A Sweet, K McDermid, H Shaw, S R Claytor, J Willis, J Kelly, D P Producer: 20010712 In: American journal of medical genetics vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular characterisation of the 22q13 deletion syndrome supports the role of haploinsufficiency of SHANK3/PROSAP2 in the major neurological symptoms. [electronic resource] by Wilson, H L Wong, A C C Shaw, S R Tse, W-Y Stapleton, G A Phelan, M C Hu, S Marshall, J McDermid, H E Producer: 20031103 In: Journal of medical genetics vol. 40 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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