Literature DB >> 10723761

Dyschromatosis universalis hereditaria: a unique disorder.

G Sethuraman, D M Thappa, J Kumar, S Srinivasan.   

Abstract

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Year:  2000        PMID： 10723761     DOI： 10.1046/j.1525-1470.2000.00011-2.x

Source DB:  PubMed          Journal:  Pediatr Dermatol        ISSN： 0736-8046            Impact factor:   1.588


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  2 in total

1.  Amyloidosis cutis dyschromica.

Authors:  Jianjun Qiao; Hong Fang; Hongtian Yao
Journal:  Orphanet J Rare Dis       Date:  2012-12-12       Impact factor: 4.123

2.  Differential Diagnosis of Two Chinese Families with Dyschromatoses by Targeted Gene Sequencing.

Authors:  Jia-Wei Liu; Jun Sun; Sergio Vano-Galvan; Feng-Xia Liu; Xiu-Xiu Wei; Dong-Lai Ma
Journal:  Chin Med J (Engl)       Date:  2016-01-05       Impact factor: 2.628
  2 in total

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