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	1.	Hypoxia-inducible factor 1alpha polymorphism and coronary collaterals in patients with ischemic heart disease. [electronic resource] by Resar, Jon R Roguin, Ariel Voner, Jeffery Nasir, Khurram Hennebry, Thomas A Miller, Julie M Ingersoll, Roxann Kasch, Laura M Semenza, Gregg L Producer: 20050906 In: Chest vol. 128 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes. [electronic resource] by Hamvas, Aaron Nogee, Lawrence M Wegner, Daniel J Depass, Kelcey Christodoulou, John Bennetts, Bruce McQuade, Leon R Gray, Peter H Deterding, Robin R Carroll, Travis R Kammesheidt, Anja Kasch, Laura M Kulkarni, Shashikant Cole, F Sessions Producer: 20100107 In: The Journal of pediatrics vol. 155 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification of an HMGB3 frameshift mutation in a family with an X-linked colobomatous microphthalmia syndrome using whole-genome and X-exome sequencing. [electronic resource] by Scott, Alan F Mohr, David W Kasch, Laura M Barton, Jill A Pittiglio, Raquel Ingersoll, Roxann Craig, Brian Marosy, Beth A Doheny, Kimberly F Bromley, William C Roderick, Thomas H Chassaing, Nicolas Calvas, Patrick Prabhu, Shreya S Jabs, Ethylin Wang Producer: 20150212 In: JAMA ophthalmology vol. 132 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)