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The British Journal of Dermatology|March 27, 2007
Keratitis-ichthyosis-deafness syndrome: disease expression and spectrum of connexin 26 (GJB2) mutations in 14 patientsJ Mazereeuw-Hautier, E Bitoun, J Chevrant-Breton, et al.The British Journal of Dermatology|May 8, 1999
Skin fragility and hypohidrotic ectodermal dysplasia resulting from ablation of plakophilin 1J A McGrath, P H Hoeger, A M Christiano, et al.The British Journal of Dermatology|January 29, 2000
Cyclosporin for severe childhood atopic dermatitis: short course versus continuous therapyJ I Harper, I Ahmed, G Barclay, et al.Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|September 12, 2006
Killed Mycobacterium vaccae suspension in children with moderate-to-severe atopic dermatitis: a randomized, double-blind, placebo-controlled trialJ Berth-Jones, P D Arkwright, D Marasovic, et al.Journal of Medical Genetics|February 4, 2005
Four common glomulin mutations cause two thirds of glomuvenous malformations ("familial glomangiomas"): evidence for a founder effectP Brouillard, M Ghassibé, A Penington, et al.American Journal of Human Genetics|March 11, 2000
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mappingS Chavanas, C Garner, C Bodemer, et al.Pageof 11