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Shengxin Xu

Showing results (11-20 of 15) with videos related to

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Journal of Dermatological Science|December 1, 2006
HLA haplotypic association with different phenotype of alopecia areata in Chinese HansFeng-Li Xiao, Sen Yang, Guo-Shu Lin, et al.
Acta Dermato-Venereologica|February 20, 2010
Platelet-derived growth factor receptor alpha gene mutations in vitiligo vulgarisShengxin Xu, Youwen Zhou, Sen Yang, et al.
Plos Genetics|June 23, 2009
Genetic variation of promoter sequence modulates XBP1 expression and genetic risk for vitiligoYunqing Ren, Sen Yang, Shengxin Xu, et al.
Clinical Science (London, England : 1979)|November 26, 2013
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)Mark Glover, James S Ware, Amanda Henry, et al.
Nature Genetics|February 7, 2018
CLCN2 chloride channel mutations in familial hyperaldosteronism type IIUte I Scholl, Gabriel Stölting, Julia Schewe, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
Journal of Dermatological Science|December 1, 2006
HLA haplotypic association with different phenotype of alopecia areata in Chinese HansFeng-Li Xiao, Sen Yang, Guo-Shu Lin, et al.
Acta Dermato-Venereologica|February 20, 2010
Platelet-derived growth factor receptor alpha gene mutations in vitiligo vulgarisShengxin Xu, Youwen Zhou, Sen Yang, et al.
Plos Genetics|June 23, 2009
Genetic variation of promoter sequence modulates XBP1 expression and genetic risk for vitiligoYunqing Ren, Sen Yang, Shengxin Xu, et al.
Clinical Science (London, England : 1979)|November 26, 2013
Detection of mutations in KLHL3 and CUL3 in families with FHHt (familial hyperkalaemic hypertension or Gordon's syndrome)Mark Glover, James S Ware, Amanda Henry, et al.
Nature Genetics|February 7, 2018
CLCN2 chloride channel mutations in familial hyperaldosteronism type IIUte I Scholl, Gabriel Stölting, Julia Schewe, et al.
Pageof 2