Literature DB >> 4430495

Hyperkeratosis lenticularis perstans (Flegel). An autosomal dominant skin disease due to lack of a keratinocytic organelle.

E Frenk, B Tapernoux.   

Abstract

Entities:  

Mesh：

Substances：

Year:  1974        PMID： 4430495

Source DB:  PubMed          Journal:  Humangenetik        ISSN： 0018-7348


× No keyword cloud information.
  4 in total

1.  [Hyperkeratosis lenticularis perstans].

Authors:  H FLEGEL
Journal:  Hautarzt       Date:  1958-08       Impact factor: 0.751

2.  Familial hyperkeratosis lenticularis perstans associated with tumours of the skin.

Authors:  G W Beveridge; A O Langlands
Journal:  Br J Dermatol       Date:  1973-05       Impact factor: 9.302

3.  The genetics of hyperkeratosis lenticularis perstans.

Authors:  S F Bean
Journal:  Arch Dermatol       Date:  1972-07

4.  Hyperkeratosis lenticularis perstans. A clinical, histopathologic, and genetic study.

Authors:  S F Bean
Journal:  Arch Dermatol       Date:  1969-06
  4 in total
  1 in total

1.  Hyperkeratosis lenticularis perstans: case report of a rare entity.

Authors:  Krina B Patel
Journal:  Indian J Dermatol       Date:  2013-03       Impact factor: 1.494
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.