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	1.	The screening of SLC6A8 deficiency among Estonian families with X-linked mental retardation. [electronic resource] by Puusepp, H Kall, K Salomons, G S Talvik, I Männamaa, M Rein, R Jakobs, C Õunap, K Producer: 20140408 In: Journal of inherited metabolic disease vol. 33 Suppl 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families. [electronic resource] by Zilina, O Reimand, T Zjablovskaja, P Männik, K Männamaa, M Traat, A Puusepp-Benazzouz, H Kurg, A Ounap, K Producer: 20130620 In: American journal of medical genetics. Part A vol. 158A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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