OpenURL Connection Search

Select item for more details and to access through your institution.

A novel GJB3 (Cx31) missense mutation in a Chinese patient with erythrokeratodermia variabilis.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2011, v. 25, n. 1, p. 113, doi. 10.1111/j.1468-3083.2010.03691.x
By:
- Wang, Z.-X.;
- Lu, W.-S.;
- Li, H.;
- Lin, D.;
- Zhou, F.-S.;
- Sun, L.-D.;
- Yang, S.;
- Zhang, X.-J.
Publication type:
Article
The effect of overweight and obesity on psoriasis patients in Chinese Han population: a hospital-based study.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2011, v. 25, n. 1, p. 87, doi. 10.1111/j.1468-3083.2010.03706.x
By:
- Zhang, C.;
- Zhu, K. J.;
- Zheng, H. F.;
- Cui, Y.;
- Zhou, F. S.;
- Chen, Y. L.;
- Tang, X. F.;
- Li, M.;
- Zhang, F. Y.;
- Fan, X.;
- Zuo, X. B.;
- Yang, S.;
- Sun, L. D.;
- Zhang, X. J.
Publication type:
Article
Novel missense mutation of keratin in Chinese family with steatocystoma multiplex.
Published in:
2009
By:
- Wang, J.-F.;
- Lu, W.-S.;
- Sun, L.-D.;
- Lv, Y.-M.;
- Zhou, F.-S.;
- Fang, Q.-Y.;
- Tang, H.-Y.;
- Cui, Y.;
- Yang, S.;
- Zhang, X.-J
Publication type:
Letter
Association of HLA haplotype with alopecia areata in Chinese Hans.
Published in:
Journal of the European Academy of Dermatology & Venereology, 2006, v. 20, n. 10, p. 1207, doi. 10.1111/j.1468-3083.2006.01750.x
By:
- Xiao, F.-L.;
- Ye, D.-Q.;
- Yang, S.;
- Zhou, F.-S.;
- Zhou, S.-M.;
- Zhu, Y.-G.;
- Liang, Y.-H.;
- Ren, Y.-Q.;
- Zhang, X.-J.
Publication type:
Article
Novel and recurrent keratin 6A ( KRT6A) mutations in Chinese patients with pachyonychia congenita type 1.
Published in:
British Journal of Dermatology, 2009, v. 160, n. 6, p. 1327, doi. 10.1111/j.1365-2133.2009.09062.x
By:
- Lv, Y. M.;
- Yang, S.;
- Zhang, Z.;
- Cui, Y.;
- Quan, C.;
- Zhou, F. S.;
- Fang, Q. Y.;
- Du, W. H.;
- Zhang, F. R.;
- Chang, J. M.;
- Tao, X. P.;
- Zhang, A.L.;
- Kang, R. H.;
- Du, W. D.;
- Zhang, X. J.
Publication type:
Article
A novel deletion mutation in the LPAR6 gene underlies autosomal recessive woolly hair with hypotrichosis.
Published in:
Clinical & Experimental Dermatology, 2013, v. 38, n. 7, p. 796, doi. 10.1111/ced.12129
By:
- Liu, L. H.;
- Chen, G.;
- Wang, J. W.;
- Liu, S. X.;
- Wang, J. B.;
- Zhou, F. S.;
- Zhu, J.;
- Sun, L. D.;
- Gao, M.;
- Wang, P. G.;
- Yang, S.;
- Zhang, X. J.
Publication type:
Article
A missense mutation in the GJB3 gene responsible for erythrokeratodermia variabilis in a Chinese family.
Published in:
Clinical & Experimental Dermatology, 2012, v. 37, n. 8, p. 919, doi. 10.1111/j.1365-2230.2012.04406.x
By:
- Wang, W.;
- Liu, L. H.;
- Chen, G.;
- Gao, M.;
- Zhu, J.;
- Zhou, F. S.;
- Cheng, H.;
- Tang, H. Y.;
- Wu, B. Y.;
- Sun, L. D.;
- Yang, S.;
- Wang, P. G.;
- Zhang, X. J.
Publication type:
Article
One novel and two recurrent mutations in the keratin 5 gene identified in Chinese patients with epidermolysis bullosa simplex.
Published in:
Clinical & Experimental Dermatology, 2009, v. 34, n. 8, p. e957, doi. 10.1111/j.1365-2230.2009.03703.x
By:
- Tang, H. Y.;
- Du, W. D.;
- Cui, Y.;
- Fan, X.;
- Quan, C.;
- Fang, Q. Y.;
- Zhou, F. S.;
- Yao, F. M.;
- Wang, J. F.;
- Yang, S.;
- Zhang, X.
Publication type:
Article
A novel frameshift mutation of the EDA1 gene in a Chinese Han family with X-linked hypohidrotic ectodermal dysplasia.
Published in:
Clinical & Experimental Dermatology, 2009, v. 34, n. 1, p. 74, doi. 10.1111/j.1365-2230.2008.02844.x
By:
- Zhang, H.;
- Quan, C.;
- Sun, L.-D.;
- Lv, H.-L.;
- Gao, M.;
- Zhou, F.-S.;
- Xiao, F.-L.;
- Fang, Q.-Y.;
- Shen, Y.-J.;
- Zhou, L.;
- Yang, S.;
- Zhang, X.-J.
Publication type:
Article

Found: 9