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	1.	Ultrastructural features of the osteoid of patients with fibrogenesis imperfecta ossium. [electronic resource] by Ralphs, J R Stamp, T C Dopping-Hepenstal, P J Ali, S Y Producer: 19891221 In: Bone vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The composition of wide-spaced collagen in normal and diseased Descemet's membrane. [electronic resource] by Levy, S G Moss, J Sawada, H Dopping-Hepenstal, P J McCartney, A C Producer: 19960702 In: Current eye research vol. 15 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Limitation of substratum size alters cytoskeletal organization and behaviour of Swiss 3T3 fibroblasts. [electronic resource] by Ireland, G W Dopping-Hepenstal, P J Jordan, P W O'Neill, C H Producer: 19891219 In: Cell biology international reports vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Descemet's membrane in the iridocorneal-endothelial syndrome: morphology and composition. [electronic resource] by Levy, S G McCartney, A C Sawada, H Dopping-Hepenstal, P J Alexander, R A Moss, J Producer: 19951122 In: Experimental eye research vol. 61 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Striate palmoplantar keratoderma resulting from desmoplakin haploinsufficiency. [electronic resource] by Whittock, N V Ashton, G H Dopping-Hepenstal, P J Gratian, M J Keane, F M Eady, R A McGrath, J A Producer: 20000113 In: The Journal of investigative dermatology vol. 113 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Transient bullous dermolysis of the newborn in three generations. [electronic resource] by Fassihi, H Diba, V C Wessagowit, V Dopping-Hepenstal, P J C Jones, C A Burrows, N P McGrath, J A Producer: 20060203 In: The British journal of dermatology vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Loricrin mutation in Vohwinkel's keratoderma is unique to the variant with ichthyosis. [electronic resource] by Korge, B P Ishida-Yamamoto, A Pünter, C Dopping-Hepenstal, P J Iizuka, H Stephenson, A Eady, R A Munro, C S Producer: 19971023 In: The Journal of investigative dermatology vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Expression in yeast of amino-terminal peptide fusions to hepatitis B core antigen and their immunological properties. [electronic resource] by Beesley, K M Francis, M J Clarke, B E Beesley, J E Dopping-Hepenstal, P J Clare, J J Brown, F Romanos, M A Producer: 19901214 In: Bio/technology (Nature Publishing Company) vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Autosomal dominant junctional epidermolysis bullosa. [electronic resource] by Almaani, N Liu, L Dopping-Hepenstal, P J C Lovell, P A Lai-Cheong, J E Graham, R M Mellerio, J E McGrath, J A Producer: 20090715 In: The British journal of dermatology vol. 160 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	A functional "knockout" of human keratin 14. [electronic resource] by Rugg, E L McLean, W H Lane, E B Pitera, R McMillan, J R Dopping-Hepenstal, P J Navsaria, H A Leigh, I M Eady, R A Producer: 19941215 In: Genes & development vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Keratin 16 and keratin 17 mutations cause pachyonychia congenita. [electronic resource] by McLean, W H Rugg, E L Lunny, D P Morley, S M Lane, E B Swensson, O Dopping-Hepenstal, P J Griffiths, W A Eady, R A Higgins, C Producer: 19950712 In: Nature genetics vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE). [electronic resource] by McLean, W H Eady, R A Dopping-Hepenstal, P J McMillan, J R Leigh, I M Navsaria, H A Higgins, C Harper, J I Paige, D G Morley, S M Producer: 19940223 In: The Journal of investigative dermatology vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Prenatal diagnosis for severe inherited skin disorders: 25 years' experience. [electronic resource] by Fassihi, H Eady, R A J Mellerio, J E Ashton, G H S Dopping-Hepenstal, P J C Denyer, J E Nicolaides, K H Rodeck, C H McGrath, J A Producer: 20060530 In: The British journal of dermatology vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1. [electronic resource] by McGrath, J A Hoeger, P H Christiano, A M McMillan, J R Mellerio, J E Ashton, G H Dopping-Hepenstal, P J Lake, B D Leigh, I M Harper, J I Eady, R A Producer: 20000317 In: The British journal of dermatology vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Striate palmoplantar keratoderma arising from desmoplakin and desmoglein 1 mutations is associated with contrasting perturbations of desmosomes and the keratin filament network. [electronic resource] by Wan, H Dopping-Hepenstal, P J C Gratian, M J Stone, M G Zhu, G Purkis, P E South, A P Keane, F Armstrong, D K B Buxton, R S McGrath, J A Eady, R A J Producer: 20040715 In: The British journal of dermatology vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma. [electronic resource] by Hunt, D M Rickman, L Whittock, N V Eady, R A Simrak, D Dopping-Hepenstal, P J Stevens, H P Armstrong, D K Hennies, H C Küster, W Hughes, A E Arnemann, J Leigh, I M McGrath, J A Kelsell, D P Buxton, R S Producer: 20010621 In: European journal of human genetics : EJHG vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)