Source: American Journal of Human Genetics. Unidade: FMRP
Subjects: MACROSTOMIA, DISPLASIA ECTODÉRMICA, GENÉTICA
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MARCHEGIANI, Shannon et al. Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and barber-say syndromes. American Journal of Human Genetics, v. 97, n. 1, p. 99-110, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.ajhg.2015.05.017. Acesso em: 10 jun. 2024.APA
Marchegiani, S., Davis, T., Tessadori, F., Haaften, G. van, Brancati, F., Hoischen, A., et al. (2015). Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and barber-say syndromes. American Journal of Human Genetics, 97( 1), 99-110. doi:10.1016/j.ajhg.2015.05.017NLM
Marchegiani S, Davis T, Tessadori F, Haaften G van, Brancati F, Hoischen A, Huang H, Valkanas E, Pusey B, Schanze D, Venselaar H, Vulto-van Silfhout AT, Wolfe LA, Tifft CJ, Zerfas PM, Zambruno G, Kariminejad A, Sabbagh-Kermani F, Lee J, Tsokos MG, Lee C-CR, Ferraz VE de F, Silva EM da, Stevens CA, Roche N, Bartsch O, Farndon P, Bermejo-Sanchez E, Brooks BP, Maduro V, Dallapiccola B, Ramos FJ, Chung H-YB, Le Caignec C, Martins F, Jacyk WK, Mazzanti L, Brunner HG, Bakkers J, Lin S, Malicdan MCV, Boerkoel CF, Gahl WA, Vries BBA de, Mieke M. van Haelst, Zenker M, Markello TC. Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and barber-say syndromes [Internet]. American Journal of Human Genetics. 2015 ; 97( 1): 99-110.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.ajhg.2015.05.017Vancouver
Marchegiani S, Davis T, Tessadori F, Haaften G van, Brancati F, Hoischen A, Huang H, Valkanas E, Pusey B, Schanze D, Venselaar H, Vulto-van Silfhout AT, Wolfe LA, Tifft CJ, Zerfas PM, Zambruno G, Kariminejad A, Sabbagh-Kermani F, Lee J, Tsokos MG, Lee C-CR, Ferraz VE de F, Silva EM da, Stevens CA, Roche N, Bartsch O, Farndon P, Bermejo-Sanchez E, Brooks BP, Maduro V, Dallapiccola B, Ramos FJ, Chung H-YB, Le Caignec C, Martins F, Jacyk WK, Mazzanti L, Brunner HG, Bakkers J, Lin S, Malicdan MCV, Boerkoel CF, Gahl WA, Vries BBA de, Mieke M. van Haelst, Zenker M, Markello TC. Recurrent mutations in the basic domain of TWIST2 cause ablepharon macrostomia and barber-say syndromes [Internet]. American Journal of Human Genetics. 2015 ; 97( 1): 99-110.[citado 2024 jun. 10 ] Available from: https://doi.org/10.1016/j.ajhg.2015.05.017
