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	1.	Report on the p.Ser489X (p.Ser489*) CFTR mutation, a variant with severe associated phenotype and high prevalence in a Quebec French-Canadian cystic fibrosis patient population. [electronic resource] by De Bie, Isabelle Agatep, Ron Scott, Patrick Ruchon, Andrea Producer: 20130211 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Role of abnormal neutral endopeptidase-like activities in Hyp mouse bone cells in renal phosphate transport. [electronic resource] by Dubois, Stéphanie G Ruchon, Andréa Frota Delalandre, Aline Boileau, Guy Lajeunesse, Daniel Producer: 20021112 In: American journal of physiology. Cell physiology vol. 283 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Frequency and phenotypic consequences of the 3199del6 CFTR mutation in French Canadians. [electronic resource] by Ruchon, Andrea Frota Ryan, Shannon R Fetni, Raouf Rozen, Rima Scott, Patrick Producer: 20050705 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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