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	1.	Molecular analysis of the rhodopsin gene in southern France: identification of the first duplication responsible for retinitis pigmentosa, c.998999ins4. [electronic resource] by Bareil, C Hamel, C Pallarès-Ruiz, N Arnaud, B Demaille, J Claustres, M Producer: 19991203 In: Ophthalmic genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Complete mutational screening of the cystic fibrosis transmembrane conductance regulator gene: cystic fibrosis mutations are not involved in healthy men with reduced sperm quality. [electronic resource] by Pallares-Ruiz, N Carles, S Des Georges, M Guittard, C Arnal, F Humeau, C Claustres, M Producer: 20000113 In: Human reproduction (Oxford, England) vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Is isolated idiopathic pancreatitis associated with CFTR mutations? [electronic resource] by Pallares-Ruiz, N Carles, S des Georges, M Guittard, C Claustres, M Larrey, D Pageaux, G Producer: 20000216 In: Gut vol. 46 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A naturally occurring sequence variation that creates a YY1 element is associated with increased cystic fibrosis transmembrane conductance regulator gene expression. [electronic resource] by Romey, M C Pallares-Ruiz, N Mange, A Mettling, C Peytavi, R Demaille, J Claustres, M Producer: 20000302 In: The Journal of biological chemistry vol. 275 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Evaluation of dHPLC for CX26 mutation screening in patients from southern France with sensorineural deafness. [electronic resource] by Pallares-Ruiz, N Blanchet, P Mondain, M Low-Hong, S Demaille, J Claustres, M Roux, A F Producer: 20020515 In: Genetic testing vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Survey of the frequency of USH1 gene mutations in a cohort of Usher patients shows the importance of cadherin 23 and protocadherin 15 genes and establishes a detection rate of above 90%. [electronic resource] by Roux, A-F Faugère, V Le Guédard, S Pallares-Ruiz, N Vielle, A Chambert, S Marlin, S Hamel, C Gilbert, B Malcolm, S Claustres, M Producer: 20070103 In: Journal of medical genetics vol. 43 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	A new approach for identifying non-pathogenic mutations. An analysis of the cystic fibrosis transmembrane regulator gene in normal individuals. [electronic resource] by Bombieri, C Giorgi, S Carles, S de Cid, R Belpinati, F Tandoi, C Pallares-Ruiz, N Lazaro, C Ciminelli, B M Romey, M C Casals, T Pompei, F Gandini, G Claustres, M Estivill, X Pignatti, P F Modiano, G Producer: 20000413 In: Human genetics vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)