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	1.	Two children with subtelomeric 11q deletions: a description and interpretation of their clinical presentations and molecular genetic findings. [electronic resource] by Cox, Helen Lucassen, Anneke Rio, Marlene Browne, Caroline Renforth, Glenn Craven, Lyndsey Salmon, Tony Wilson, David I Producer: 20090528 In: Clinical dysmorphology vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Subcellular localization of ALMS1 supports involvement of centrosome and basal body dysfunction in the pathogenesis of obesity, insulin resistance, and type 2 diabetes. [electronic resource] by Hearn, Tom Spalluto, Cosma Phillips, Victoria J Renforth, Glenn L Copin, Nane Hanley, Neil A Wilson, David I Producer: 20050705 In: Diabetes vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Mutation of ALMS1, a large gene with a tandem repeat encoding 47 amino acids, causes Alström syndrome. [electronic resource] by Hearn, Tom Renforth, Glenn L Spalluto, Cosma Hanley, Neil A Piper, Karen Brickwood, Sarah White, Chris Connolly, Vincent Taylor, James F N Russell-Eggitt, Isabelle Bonneau, Dominque Walker, Mark Wilson, David I Producer: 20020528 In: Nature genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Narrowing the critical region within 11q24-qter for hypoplastic left heart and identification of a candidate gene, JAM3, expressed during cardiogenesis. [electronic resource] by Phillips, Helen M Renforth, Glenn L Spalluto, Cosma Hearn, Tom Curtis, Andrew R J Craven, Lyndsey Havarani, Beatrice Clement-Jones, Mark English, Carol Stumper, Oliver Salmon, Tony Hutchinson, Susie Jackson, Mike S Wilson, David I Producer: 20020816 In: Genomics vol. 79 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)