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The British Journal of Dermatology|August 19, 2016
Mutations in desmoglein 1 cause diverse inherited palmoplantar keratoderma phenotypes: implications for genetic screeningM-L Lovgren, M A McAleer, A D Irvine, et al.Allergy|March 1, 2008
Filaggrin null mutations are associated with increased asthma exacerbations in children and young adultsK Basu, C N A Palmer, B J Lipworth, et al.The British Journal of Ophthalmology|June 27, 2002
A novel mutation in KRT12 associated with Meesmann's epithelial corneal dystrophyA D Irvine, C M Coleman, J E Moore, et al.The British Journal of Dermatology|March 12, 2014
The molecular genetic analysis of the expanding pachyonychia congenita case collectionN J Wilson, E A O'Toole, L M Milstone, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|July 17, 2016
Mutations in the mevalonate pathway genes in Chinese patients with porokeratosisM Li, Z Li, J Wang, et al.Pageof 2