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2019.2-18.Dyschromatosis

Dyschromatosis universalis hereditaria: A rare case report from Northeast India Romita Bachaspatimayum, Priyanka Das, Nandita Bhattacharjee Department of Dermatology, Venereology and Leprology, Regional Institute of Medical Sciences, Imphal, Manipur, India Corresponding author: Dr. Priyanka Das, E-mail: iampriyanka1243@gmail.com Submission: 20.06.2018; Acceptance: 20.08.2018 DOI:10.7241/ourd.20192.18 Cite this article: Bachaspatimayum R, Das P, Bhattacharjee N. Dyschromatosis universalis hereditaria: A rare […]

Issue 2019.2

since 09. April 2019 C O N T E N T S   2.2019     The proportion of research articles supported by research funds 0% The proportion of articles written by editorial board members as corresponding authors 8,57% The number of authors’ countries 22 Original Articles 5 (14%) Brief Report 2 (6%) Case Reports 14 (40%)  […]


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