Syndrome de Goltz chez un nouveau-né avec fente labiopalatine-Reference-Cited by-同舟云学术

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Syndrome de Goltz chez un nouveau-né avec fente labiopalatine

Published:2012-02 Issue:2 Volume:19 Page:160-162
ISSN:0929-693X
Container-title:Archives de Pédiatrie
language:fr
Short-container-title:Archives de Pédiatrie

Author:

Nagalo K.,Laberge J.-M.,Nguyen V.-H.,Laberge-Caouette L.,Turgeon J.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference10 articles.

1. Deficiency of PORCN, a regulator of Wnt signaling, is associated with focal dermal hypoplasia;Grzeschik;Nat Genet,2007

2. Focal dermal hypoplasia;Goltz;Arch Dermatol,1962

3. Focal dermal hypoplasia syndrome: an update;Goltz;Arch Dermatol,1992

4. Aplasia cutis congenita associated with Goltz syndrome in a male neonate;Gnamey;Genet Couns,2010

5. Goltz syndrome (focal dermal hypoplasia) with unilateral ocular, cutaneous and skeletal features: case report;Tenkir;BMC Ophthalmol,2010

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1. Gender and Genodermatoses;Gender and Dermatology;2018

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