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Citation: M. Liovic et al., A novel keratin 5 mutation (K5V186L) in a family with EBS-K: a conservative substitution can lead to development of different disease phenotypes, J INVES DER, 116(6), 2001, pp. 964-969

Authors: Virtanen, M Gedde-Dahl, T Mork, NJ Leigh, I Bowden, PE Vahlquist, A

Citation: M. Virtanen et al., Phenotypic/genotypic correlations in patients with epidermolytic hyperkeratosis and the effects of retinoid therapy on keratin expression, ACT DER-VEN, 81(3), 2001, pp. 163-170

Authors: Bowden, PE

Citation: Pe. Bowden, Design and selection of mechanical seals to minimize emissions, P I MEC E J, 213(J3), 1999, pp. 177-188

Authors: Lin, MTS Levy, ML Bowden, PE Magro, C Baden, L Baden, HP Roop, DR

Citation: Mts. Lin et al., Identification of sporadic mutations in the helix initiation motif of keratin 6 in two pachyonychia congenita patients: further evidence for a mutational hot spot, EXP DERMATO, 8(2), 1999, pp. 115-119

Authors: McLean, WHI Morley, SM Higgins, C Bowden, PE White, M Leigh, IM Lane, EB

Citation: Whi. Mclean et al., Novel and recurrent mutations in keratin 10 causing bullous congenital ichthyosiform erythroderma, EXP DERMATO, 8(2), 1999, pp. 120-123

Authors: Pearce, EG Smith, SK Lanigan, SW Bowden, PE

Citation: Eg. Pearce et al., Two different mutations in the same codon of a type II hair keratin (hHb6)in patients with monilethrix, J INVES DER, 113(6), 1999, pp. 1123-1127