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	1.	A founder mutation for ichthyosis prematurity syndrome restricted to 76 kb by haplotype association. [electronic resource] by Melin, M Klar, J Jr Gedde-Dahl, T Fredriksson, R Hausser, I Brandrup, F Bygum, A Vahlquist, A Hellström Pigg, M Dahl, N Producer: 20061211 In: Journal of human genetics vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by DSP mutations. [electronic resource] by Vahlquist, A Virtanen, M Hellström-Pigg, M Dragomir, A Ryberg, K Wilson, N J Östman--Smith, I Lu, L McGrath, J A Smith, F J D Producer: 20140925 In: Clinical and experimental dermatology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Novel and recurring ABCA12 mutations associated with harlequin ichthyosis: implications for prenatal diagnosis. [electronic resource] by Thomas, A C Sinclair, C Mahmud, N Cullup, T Mellerio, J E Harper, J Dale, B A Turc-Carel, C Hohl, D McGrath, J A Vahlquist, A Hellstrom-Pigg, M Ganemo, A Metcalfe, K Mein, C A O'Toole, E A Kelsell, D P Producer: 20080428 In: The British journal of dermatology vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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