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Clinical and Experimental Dermatology|July 24, 2012
MBTPS2 mutation in a British pedigree with keratosis follicularis spinulosa decalvansK Fong, E K Wedgeworth, J E Lai-Cheong, et al.
The British Journal of Dermatology|January 6, 2009
Kindler syndrome: a focal adhesion genodermatosisJ E Lai-Cheong, A Tanaka, G Hawche, et al.
Clinical and Experimental Dermatology|February 4, 2012
Infantile systemic hyalinosis associated with a putative splice-site mutation in the ANTXR2 geneK Fong, A R Rama Devi, J E Lai-Cheong, et al.
The British Journal of Dermatology|September 15, 2007
Unusual molecular findings in Kindler syndromeK Arita, V Wessagowit, A C Inamadar, et al.
The British Journal of Dermatology|January 6, 2009
Autosomal dominant junctional epidermolysis bullosaN Almaani, L Liu, P J C Dopping-Hepenstal, et al.
The British Journal of Dermatology|February 15, 2012
Mutations in AEC syndrome skin reveal a role for p63 in basement membrane adhesion, skin barrier integrity and hair follicle biologyS E Clements, T Techanukul, J E Lai-Cheong, et al.
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