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  • 2020
  • 2018
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Author

  • Sheau-Chiou Chao
2018

Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in WNT10A

Hsu, T. C., Lee, J. Y. Y., Hsu, M. M. L. & Chao, S. C., 2018 Apr, In : Journal of Dermatology. 45, 4, p. 475-478 4 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Cerebrotendinous xanthomatosis-a case report with novel compound heterozygous mutation of CYP27A1 gene

Yuan, J., Sung, P. S., Lee, J. Y. Y. & Chao, S. C., 2018 Dec, In : Dermatologica Sinica. 36, 4, p. 200-202 3 p.

Research output: Contribution to journalArticle

Generalized Dowling-Degos disease with an initiation codon mutation of KRT5 mutation

Hsieh, F. N., Chao, S. C. & Lee, J. Y. Y., 2018 Jun, In : Dermatologica Sinica. 36, 2, p. 103-104 2 p.

Research output: Contribution to journalLetter

2020

Plectin missense mutation p.Leu319pro in the pathogenesis of autosomal recessive epidermolysis bullosa simplex

Tu, W. T., Chen, P. C., Hou, P. C., Huang, H. Y., Wang, J. Y., Chao, S. C., Lee, J. Y. Y., McGrath, J. A., Natsuga, K. & Hsu, C. K., 2020 Aug, In : Acta Dermato-Venereologica. 100, 15, p. 1-2 2 p., adv00242.

Research output: Contribution to journalArticle

Open Access