Literature DB >> 4298032

[A gene dysplasia not previously known: frequently degenerative sclero-atrophying and keratodermic genodermatosis of the extremities].

C Huriez, M Deminatti, P Agache, M Mennecier.   

Abstract

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Mesh：

Year:  1968        PMID： 4298032

Source DB:  PubMed          Journal:  Sem Hop


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  4 in total

1.  A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23.

Authors:  Y A Lee; H P Stevens; E Delaporte; U Wahn; A Reis
Journal:  Am J Hum Genet       Date:  2000-01       Impact factor: 11.025

2.  Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24.

Authors:  A Martinez-Mir; A Zlotogorski; D Londono; D Gordon; A Grunn; E Uribe; L Horev; I M Ruiz; N O Davalos; O Alayan; J Liu; T C Gilliam; J C Salas-Alanis; A M Christiano
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

3.  The diffuse and macular atrophic dermatosis. A precocious and progressive light degenerative condition.

Authors:  D Stevanović
Journal:  Arch Dermatol Res       Date:  1979-05-29       Impact factor: 3.017

4.  Huriez syndrome with superadded dermatophyte infection.

Authors:  Trupti Surana; Bela Padhiar; Umesh Karia; Purna Pandya
Journal:  Indian Dermatol Online J       Date:  2016 Jul-Aug
  4 in total

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