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Springer International Publishing
Reference91 articles.
1. Tallman B, Tan OT, Morelli JG, et al. Location of port-wine stains and the likelihood of ophthalmic and/or central nervous system complications. Pediatrics. 1991;87:323–32.
2. Pedailles S, Martin N, Launay V, et al. [Sturge-Weber-Krabbe syndrome. A severe form in a monozygote female twin]. Ann Dermatol Venereol. 1993;120:379–82.
3. Panteliadis CP, Benjamin R, Cremer H-J, et al., editors. Neurocutaneous disorders—haemangiomas—a clinical and diagnostic approach. London: Anshan; 2007.
4. Happle R. Lethal genes surviving by mosaicism: a possible explanation for sporadic birth defects involving the skin. J Am Acad Dermatol. 1987;16:899–906.
5. Shirley MD, Tang H, Gallione CJ, et al. Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ. N Engl J Med. 2013;368:1971–9.