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The British Journal of Dermatology|February 21, 1998
Recessive epidermolysis bullosa simplex associated with plectin mutations: infantile respiratory complications in two unrelated casesJ E Mellerio, F J Smith, J R McMillan, et al.Diabetes & Metabolism|September 20, 2015
Potential influence of Type A personality on plasma C-reactive protein levels in people with diabetesJ-C Chauvet-Gélinier, B Trojak, C Lemogne, et al.JAMA Dermatology|April 14, 2017
Expanding the Genotypic Spectrum of Bathing Suit IchthyosisNareh V Marukian, Rong-Hua Hu, Brittany G Craiglow, et al.American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.Genes & Development|July 15, 1996
Loss of plectin causes epidermolysis bullosa with muscular dystrophy: cDNA cloning and genomic organizationW H McLean, L Pulkkinen, F J Smith, et al.Nature Genetics|August 1, 1996
Plectin deficiency results in muscular dystrophy with epidermolysis bullosaF J Smith, R A Eady, I M Leigh, et al.The Journal of Investigative Dermatology|August 21, 2001
The spectrum of pathogenic mutations in SPINK5 in 19 families with Netherton syndrome: implications for mutation detection and first case of prenatal diagnosisE Sprecher, S Chavanas, J J DiGiovanna, et al.The British Journal of Dermatology|February 5, 2020
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragilityC Has, J W Bauer, C Bodemer, et al.Journal of Molecular Medicine (Berlin, Germany)|April 12, 2000
A 500-kb region on chromosome 16p13.1 contains the pseudoxanthoma elasticum locus: high-resolution mapping and genomic structureL Cai, B Struk, M D Adams, et al.ESMO Open|November 26, 2025
PROMENADE: pembrolizumab for early ER-low/HER2-negative breast cancer, real-world French cohortF Cherifi, L Cabel, C Bousrih, et al.Pageof 67