Rothmund–Thomson Syndrome in Three Siblings and Development of Cutaneous Squamous Cell Carcinoma
Author:
Affiliation:
1. Department of Dermatology, Hospital Das Clinicas, University of São Paulo, São Paulo, Brazil
Publisher
Wiley
Subject
Dermatology,Pediatrics, Perinatology, and Child Health
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1046/j.1525-1470.2002.00089.x
Reference27 articles.
1. Uber Kataract in Vebindung mit Einer Eugntumliche Haut Degeneration [Cataracts in association with a peculiar degeneration of the skin];Rothmund A;Arch ophthalmol,1887
2. Rothmund-Thomson syndrome: Review of the world literature
3. Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome
4. Rothmund–Thomson Syndrome Responsible Gene, RECQL4: Genomic Structure and Products
5. Poiquilodermia congenita (Sindrome de Thomson);Zamith VA;Rev Paul Med,1957
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