| 1 | FENS, FGFR3
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| Fibroblast Growth Factor Receptor 3 Epidermal Naevus Syndrome with Urothelial Mosaicism for the Activating p.Ser249Cys FGFR3 Mutation.
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| Bessis D, Plaisancié J, Gaston V, Bieth E.
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| Acta Derm Venereol 97(3):402-403. doi: 10.2340/00015555-2554.
2017
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| 2 | FENS, FGFR3
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| An epidermal nevus syndrome with cerebral involvement caused by a mosaic FGFR3 mutation.
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| García-Vargas A, Hafner C, PĂ©rez-RodrĂguez AG, RodrĂguez-Rojas LX, González-Esqueda P, Stoehr R, Hernández-Torres M, Happle R.
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| Am J Med Genet A 146A(17):2275-9. 2008
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| 3 | FENS, FGFR3, HCH
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| Acanthosis nigricans in a child with mild osteochondrodysplasia and K650Q mutation in the FGFR3 gene.
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| Leroy JG, Nuytinck L, Lambert J, Naeyaert JM, Mortier GR.
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| Am J Med Genet A 143(24):3144-9. 2007
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| 4 | FENS, FGFR3
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| Mosaicism of activating FGFR3 mutations in human skin causes epidermal nevi.
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| Hafner C, van Oers JM, Vogt T, Landthaler M, Stoehr R, Blaszyk H, Hofstaedter F, Zwarthoff EC, Hartmann A.
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| J Clin Invest 116(8):2201-2207. 2006
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| 5 | FENS, FGFR3
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| High frequency of FGFR3 mutations in adenoid seborrheic keratoses.
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| Hafner C, van Oers JM, Hartmann A, Landthaler M, Stoehr R, Blaszyk H, Hofstaedter F, Zwarthoff EC, Vogt T.
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| J Invest Dermatol 126(11):2404-7. Epub 2006 Jun 15. 2006
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