Molecular evidence of type 2 mosaicism in Gorlin syndrome-Reference-Cited by-同舟云学术

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Molecular evidence of type 2 mosaicism in Gorlin syndrome

Published:2013-12 Issue:6 Volume:169 Page:1342-1345
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:Br J Dermatol

Author:

Torrelo A.¹,Hernández-Martín A.¹,Bueno E.²,Colmenero I.³,Rivera I.¹,Requena L.⁴,Happle R.⁵,González-Sarmiento R.²

Affiliation:

1. Department of Dermatology ; Hospital del Niño Jesús; Menendez Pelayo 65 Madrid 28034 Spain

2. Department of Medicine; IBMCC and IBSAL; Universidad de Salamanca-CSIC; Salamanca Spain

3. Department of Pathology; Hospital del Niño Jesús; Menendez Pelayo 65 Madrid 28034 Spain

4. Department of Dermatology; Fundación Jiménez Díaz; Madrid Spain

5. Department of Dermatology; Freiburg University Medical Center; Freiburg Germany

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/bjd.12458/fullpdf

Reference12 articles.

1. A rule concerning the segmental manifestation of autosomal dominant skin disorders. Review of clinical examples providing evidence for dichotomous types of severity;Happle;Arch Dermatol,1997

2. Superimposed segmental manifestation of both rare and common cutaneous disorders: a new paradigm;Happle;Actas Dermosifiliogr,2009

3. Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept;Poblete-Gutiérrez;J Clin Invest,2004

4. Molecular genetic support for the rule of dichotomy in type 2 segmental Darier disease;Fölster-Holst;Br J Dermatol,2012

5. Nevoid basal cell carcinoma (Gorlin) syndrome;Gorlin;Genet Med,2004

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