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The British Journal of Dermatology|April 16, 1998
Association of atopic dermatitis to the beta subunit of the high affinity immunoglobulin E receptorH E Cox, M F Moffatt, J A Faux, et al.Dermatology (Basel, Switzerland)|September 11, 2001
Cyclosporin for atopic dermatitis in childrenJ I Harper, J Berth-Jones, R D Camp, et al.American Journal of Human Genetics|October 1, 1993
A new nucleotide-excision-repair gene associated with the disorder trichothiodystrophyM Stefanini, W Vermeulen, G Weeda, et al.The Journal of Investigative Dermatology|September 1, 1994
Ichthyosis bullosa of Siemens--a disease involving keratin 2eW H McLean, S M Morley, E B Lane, et al.The British Journal of Dermatology|January 20, 1999
Pyloric atresia-junctional epidermolysis bullosa syndrome: mutations in the integrin beta4 gene (ITGB4) in two unrelated patients with mild diseaseJ E Mellerio, L Pulkkinen, J R McMillan, et al.Human Mutation|April 29, 1998
Homozygous nonsense mutation in helix 2 of K14 causes severe recessive epidermolysis bullosa simplexL D Corden, J E Mellerio, M J Gratian, et al.Nature Genetics|March 30, 2001
Genetic linkage of childhood atopic dermatitis to psoriasis susceptibility lociW O Cookson, B Ubhi, R Lawrence, et al.The Journal of Investigative Dermatology|January 1, 1994
Mutations in the rod 1A domain of keratins 1 and 10 in bullous congenital ichthyosiform erythroderma (BCIE)W H McLean, R A Eady, P J Dopping-Hepenstal, et al.Nature Genetics|September 7, 2001
Gene polymorphism in Netherton and common atopic diseaseA J Walley, S Chavanas, M F Moffatt, et al.Nature Genetics|June 3, 2000
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeS Chavanas, C Bodemer, A Rochat, et al.Pageof 11