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	1.	A new missense mutation of fibrillin in a patient with Marfan syndrome. [electronic resource] by Hewett, D R Lynch, J R Child, A Sykes, B C Producer: 19940929 In: Journal of medical genetics vol. 31 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	G/A polymorphism in an intron of the fibrillin gene FBNI. [electronic resource] by Hewett, D R Lynch, J R Godfrey, M Sykes, B C Producer: 19920211 In: Nucleic acids research vol. 19 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	A novel fibrillin mutation in the Marfan syndrome which could disrupt calcium binding of the epidermal growth factor-like module. [electronic resource] by Hewett, D R Lynch, J R Smith, R Sykes, B C Producer: 19930702 In: Human molecular genetics vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	The calcium binding properties and molecular organization of epidermal growth factor-like domains in human fibrillin-1. [electronic resource] by Handford, P Downing, A K Rao, Z Hewett, D R Sykes, B C Kielty, C M Producer: 19950425 In: The Journal of biological chemistry vol. 270 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis. [electronic resource] by Maniatis, N Collins, A Xu, C F McCarthy, L C Hewett, D R Tapper, W Ennis, S Ke, X Morton, N E Producer: 20020325 In: Proceedings of the National Academy of Sciences of the United States of America vol. 99 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	FRA10B structure reveals common elements in repeat expansion and chromosomal fragile site genesis. [electronic resource] by Hewett, D R Handt, O Hobson, L Mangelsdorf, M Eyre, H J Baker, E Sutherland, G R Schuffenhauer, S Mao, J I Richards, R I Producer: 19980727 In: Molecular cell vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. [electronic resource] by McCarthy, L C Hosford, D A Riley, J H Bird, M I White, N J Hewett, D R Peroutka, S J Griffiths, L R Boyd, P R Lea, R A Bhatti, S M Hosking, L K Hood, C M Jones, K W Handley, A R Rallan, R Lewis, K F Yeo, A J Williams, P M Priest, R C Khan, P Donnelly, C Lumsden, S M O'Sullivan, J See, C G Smart, D H Shaw-Hawkins, S Patel, J Langrish, T C Feniuk, W Knowles, R G Thomas, M Libri, V Montgomery, D S Manasco, P K Xu, C F Dykes, C Humphrey, P P Roses, A D Purvis, I J Producer: 20020221 In: Genomics vol. 78 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)