| 1 | HRAS, KRAS, BRAF, CFC2, COSTS, CFC3, MAP2K1, MAP2K2, CFC4, CFC5
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| Mutation and phenotypic spectrum in patients with cardio-facio-cutaneous and Costello syndrome.
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| Schulz AL, Albrecht B, Arici C, van der Burgt I, Buske A, Gillessen-Kaesbach G, Heller R, Horn D, HŸbner CA, Korenke GC, Kšnig R, Kress W, KrŸger G, Meinecke P, MŸcke J, Plecko B, Rossier E, Schinzel A, Schulze A, Seemanova E, Seidel H, Spranger S, Tuysuz B, Uhrig S, Wieczorek D, Kutsche K, Zenker M.
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| Clin Genet 73(1):62-70. Epub 2007 Nov 27. 2008
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| 2 | MAP2K1, MAP2K2, BRAF, CFC3, CFC4, CFC2
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| Germline mutations of MEK in cardio-facio-cutaneous syndrome are sensitive to MEK and RAF inhibition: implications for therapeutic options.
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| Senawong T, Phuchareon J, Ohara O, McCormick F, Rauen KA, Tetsu O.
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| Hum Mol Genet 17(3):419-30. Epub 2007 Nov 2. 2008
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| 3 | CFC2, CFC3, CFC4, CFC5
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| Further delineation of cardio-facio-cutaneous syndrome: clinical features of 38 individuals with proven mutations.
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| Armour CM, Allanson JE.
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| J Med Genet 45(4):249-54. Epub 2007 Nov 26. 2008
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| 4 | BRAF, CFC2, CFC3, CFC4, CFC5, COSTS, HRAS, KRAS, MAP2K1, MAP2K2, NS3
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| The RAS/MAPK syndromes: novel roles of the RAS pathway in human genetic disorders.
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| Aoki Y, Niihori T, Narumi Y, Kure S, Matsubara Y.
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| Hum Mutat 29(8):992-1006.
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| 5 | BRAF, CFC2, CFC3, COSTS, HRAS, KRAS, LEOPS, MAP2K1, MAPK1, MTOR, NF1, NFNS, NS1, NS3, NS4, NS5, PTPN11, RAF1, SOS1
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| Oncogenes on my mind: ERK and MTOR signaling in cognitive diseases.
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| Krab LC, Goorden SM, Elgersma Y.
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| Trends Genet 24(10):498-510. Epub 2008 Sep 4. 2008
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| 6 | CFC2, CFC3, CFC4, CFC5, KRAS, MAP2K1, MAP2K2, BRAF, COSTS, HRAS
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| Molecular and clinical characterization of cardio-facio-cutaneous (CFC) syndrome: overlapping clinical manifestations with Costello syndrome.
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| Narumi Y, Aoki Y, Niihori T, Neri G, Cave H, Verloes A, Nava C, Kavamura MI, Okamoto N, Kurosawa K, Hennekam RC, Wilson LC, Gillessen-Kaesbach G, Wieczorek D, Lapunzina P, Ohashi H, Makita Y, Kondo I, Tsuchiya S, Ito E, Sameshima K, Kato K, Kure S, Matsubara Y.
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| Am J Med Genet A 143(8):799-807. 2007
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| 7 | BRAF,CFC2,CFC3,MAP2K1
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| Further delineation of the phenotype resulting from BRAF or MEK1 germline mutations helps differentiate cardio-facio-cutaneous syndrome from Costello syndrome.
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| Gripp KW, Lin AE, Nicholson L, Allen W, Cramer A, Jones KL, Kutz W, Peck D, Rebolledo MA, Wheeler PG, Wilson W, Al-Rahawan MM, Stabley DL, Sol-Church K.
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| Am J Med Genet A 143(13):1472-80. 2007
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| 8 | CFC2, BRAF, CFC3, MAP21K1, CFC3, MAP2K2, CFC5, KRAS, COSTS, HRAS
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| Cardio-facio-cutaneous and Noonan syndromes due to mutations in the RAS/MAPK signalling pathway: genotype-phenotype relationships and overlap with Costello syndrome.
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| Nava C, Hanna N, Michot C, Pereira S, Pouvreau N, Niihori T, Aoki Y, Matsubara Y, Arveiler B, Lacombe D, Pasmant E, Parfait B, Baumann C, HŽron D, Sigaudy S, Toutain A, Rio M, Goldenberg A, Leheup B, Verloes A, CavŽ H.
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| J Med Genet 44(12):763-71. Epub 2007 Aug 17. 2007
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| 9 | CFC2, BRAF, RAF1, MAP2K1, MAP2K2, CFC3, CFC4
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| Germline mutations in genes within the MAPK pathway cause cardio-facio-cutaneous syndrome.
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| Rodriguez-Viciana P, Tetsu O, Tidyman WE, Estep AL, Conger BA, Cruz MS, McCormick F, Rauen KA.
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| Science 311(5765):1287-90. Epub 2006 Jan 26. 2006
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| 10 | KRAS, BRAF, CFC2
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| Germline KRAS and BRAF mutations in cardio-facio-cutaneous syndrome.
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| Niihori T, Aoki Y, Narumi Y, Neri G, Cave H, Verloes A, Okamoto N, Hennekam RC, Gillessen-Kaesbach G, Wieczorek D, Kavamura MI, Kurosawa K, Ohashi H, Wilson L, Heron D, Bonneau D, Corona G, Kaname T, Naritomi K, Baumann C, Matsumoto N, Kato K, Kure S, Matsubara Y.
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| Nat Genet 38(3):294-6. Epub 2006 Feb 12. 2006
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| 11 | CFC2, BRAF, CFC3, MAP2K1, CFC4, MAP2K2, COSTS, HRAS
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| Distinguishing Costello versus cardio-facio-cutaneous syndrome: BRAF mutations in patients with a Costello phenotype.
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| Rauen KA.
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| Am J Med Genet A 140(15):1681-3. No abstract available. 2006
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| 12 | CFC2, CFC3, CFC4
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| The cardiofaciocutaneous syndrome.
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| Roberts A, Allanson J, Jadico SK, Kavamura MI, Noonan J, Opitz JM, Young T, Neri G.
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| J Med Genet 43(11):833-42. Epub 2006 Jul 6. 2006
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