Literature DB >> 5142888

[Focal dermal hypoplasia; considerations on osteopathia striata and on the genetic problem].

M Larrègue, Y Michel, J Maroteaux, R Degos, W M Stewart.   

Abstract

Entities:  

Mesh：

Year:  1971        PMID： 5142888

Source DB:  PubMed          Journal:  Ann Dermatol Syphiligr (Paris)        ISSN： 0003-3979


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  5 in total

1.  Goltz syndrome: a rare case of father-to-daughter transmission.

Authors:  Vishal Gupta; Himabindu Saginatham; Sudheer Arava; Gomathy Sethuraman
Journal:  BMJ Case Rep       Date:  2016-08-16

2.  [Focal dermal hypoplasia with apocrine nevi and striation of bones (author's transl)].

Authors:  F Vakilzadeh; R Happle; P Peters; E Macher
Journal:  Arch Dermatol Res       Date:  1976-08-27       Impact factor: 3.017

3.  Osteopathia striata and focal dermal hypoplasia.

Authors:  D Knockaert; J Dequeker
Journal:  Skeletal Radiol       Date:  1979       Impact factor: 2.199

4.  X-linked dominant inherited diseases with lethality in hemizygous males.

Authors:  R Wettke-Schäfer; G Kantner
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

5.  Unilateral Focal Dermal Hypoplasia (Goltz Syndrome): Case Report and Literature Review.

Authors:  Sahar Alsharif; Sohad Hindi; Fay Khoja
Journal:  Case Rep Dermatol       Date:  2018-05-03
  5 in total

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