Literature DB >> 20749477

On a Rare Nodose Condition of the Hair.

W G Smith.   

Abstract

Year:  1880        PMID： 20749477      PMCID： PMC2240196          DOI： 10.1136/bmj.1.1009.654-a

Source DB:  PubMed          Journal:  Br Med J        ISSN： 0007-1447


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  2 in total

1.  [ON INFORMATION ON THE MONILETHRIX SYNDROME].

Authors:  G E HEYDT
Journal:  Arch Klin Exp Dermatol       Date:  1963-08-07

2.  A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix.

Authors:  Jin Wu; Yongli Lin; Wenrong Xu; Zhongming Li; Weixin Fan
Journal:  J Biomed Res       Date:  2011-01
  2 in total

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