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	1.	Exclusion of RAI2 as the causative gene for Nance-Horan syndrome. [electronic resource] by Walpole, S M Ronce, N Grayson, C Dessay, B Yates, J R Trump, D Toutain, A Producer: 19990723 In: Human genetics vol. 104 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	High-resolution physical map of the X-linked retinoschisis interval in Xp22. [electronic resource] by Walpole, S M Nicolaou, A Howell, G R Whittaker, A Bentley, D R Ross, M T Yates, J R Trump, D Producer: 19971103 In: Genomics vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region. [electronic resource] by Montini, E Andolfi, G Caruso, A Buchner, G Walpole, S M Mariani, M Consalez, G Trump, D Ballabio, A Franco, B Producer: 19981005 In: Genomics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22. [electronic resource] by Walpole, S M Hiriyana, K T Nicolaou, A Bingham, E L Durham, J Vaudin, M Ross, M T Yates, J R Sieving, P A Trump, D Producer: 19990524 In: Genomics vol. 55 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Characterization of SCML1, a new gene in Xp22, with homology to developmental polycomb genes. [electronic resource] by van de Vosse, E Walpole, S M Nicolaou, A van der Bent, P Cahn, A Vaudin, M Ross, M T Durham, J Pavitt, R Wilkinson, J Grafham, D Bergen, A A van Ommen, G J Yates, J R den Dunnen, J T Trump, D Producer: 19980625 In: Genomics vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)