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	1.	Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations. [electronic resource] by Russell, Mark W Raeker, Maide O Geisler, Sarah B Thomas, Peedikayil E Simmons, Tracy A Bernat, John A Thorsson, Thor Innis, Jeffrey W Producer: 20160322 In: Human molecular genetics vol. 23 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	3xTg-AD mice exhibit an activated central stress axis during early-stage pathology. [electronic resource] by Hebda-Bauer, Elaine K Simmons, Tracy A Sugg, Andrew Ural, Eren Stewart, James A Beals, James L Wei, Qiang Watson, Stanley J Akil, Huda Producer: 20130528 In: Journal of Alzheimer's disease : JAD vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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