2008-11-01
Multiple familial trichoepithelioma and familial cylindroma: One cause!
Publication
Publication
Journal of the European Academy of Dermatology and Venereology , Volume 22 - Issue 11 p. 1395- 1396
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Adolescent, CYLD gene, adult, amino acid substitution, case report, chromosome 16, chromosome 9q, chromosome deletion, clinical feature, cylindroma, exon, familial disease, family history, gene, gene sequence, genetic linkage, histopathology, human, human tissue, intron, letter, male, nucleotide sequence, pedigree, phenotype, priority journal, scoring system, trichoepithelioma | |
dx.doi.org/10.1111/j.1468-3083.2008.02648.x, hdl.handle.net/1765/14590 | |
Journal of the European Academy of Dermatology and Venereology | |
Organisation | Erasmus MC: University Medical Center Rotterdam |
Oranje, A.P, Halley, D.J.J, den Hollander, J.C, Teepe, R.G.J, van de Graaf, R, van den Ouweland, A.M.W, & Wagner, A. (2008). Multiple familial trichoepithelioma and familial cylindroma: One cause!. Journal of the European Academy of Dermatology and Venereology, 22(11), 1395–1396. doi:10.1111/j.1468-3083.2008.02648.x
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