Vissers, Lisenka E. L. M.; Cox, Timothy C.; Maga, A. Murat; Short, Kieran M.; Wiradjaja, Fenny; Janssen, Irene M.; Jehee, Fernanda Sarquis; Bertola, Débora Romeo; Liu, Jia; Yagnik, Garima; Sekiguchi, Kiyotoshi; Kiyozumi, Daiji; Bokhoven, Hans van; Marcelis, Carlo; Cunningham, Michael; Anderson, Peter J.; Boyadjiev, Simeon A; Passos-Bueno, Maria Rita 
; Veltman, Joris A; Smyth, Ian; Buckley, Michael F.; Roscioli, Tony
Fonte: PLoS Genetics. Unidade: IB
Assuntos: MUTAÇÃO GENÉTICA, CRANIOSSINOSTOSE
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VISSERS, Lisenka E. L. M. et al. Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. PLoS Genetics, v. 7, p. e1002278, 2011Tradução . . Disponível em: https://doi.org/10.1371/journal.pgen.1002278. Acesso em: 23 ago. 2024.APA
Vissers, L. E. L. M., Cox, T. C., Maga, A. M., Short, K. M., Wiradjaja, F., Janssen, I. M., et al. (2011). Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. PLoS Genetics, 7, e1002278. doi:10.1371/journal.pgen.1002278NLM
Vissers LELM, Cox TC, Maga AM, Short KM, Wiradjaja F, Janssen IM, Jehee FS, Bertola DR, Liu J, Yagnik G, Sekiguchi K, Kiyozumi D, Bokhoven H van, Marcelis C, Cunningham M, Anderson PJ, Boyadjiev SA, Passos-Bueno MR, Veltman JA, Smyth I, Buckley MF, Roscioli T. Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice [Internet]. PLoS Genetics. 2011 ; 7 e1002278.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1371/journal.pgen.1002278Vancouver
Vissers LELM, Cox TC, Maga AM, Short KM, Wiradjaja F, Janssen IM, Jehee FS, Bertola DR, Liu J, Yagnik G, Sekiguchi K, Kiyozumi D, Bokhoven H van, Marcelis C, Cunningham M, Anderson PJ, Boyadjiev SA, Passos-Bueno MR, Veltman JA, Smyth I, Buckley MF, Roscioli T. Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice [Internet]. PLoS Genetics. 2011 ; 7 e1002278.[citado 2024 ago. 23 ] Available from: https://doi.org/10.1371/journal.pgen.1002278
