Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice (2011)
- Authors:
- 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
- USP affiliated authors: BERTOLA, DÉBORA ROMEO - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidade: IB
- DOI: 10.1371/journal.pgen.1002278
- Subjects: MUTAÇÃO GENÉTICA; CRANIOSSINOSTOSE
- Language: Inglês
- Imprenta:
- Publisher place: San Francisco
- Date published: 2011
- Source:
- Título do periódico: PLoS Genetics
- ISSN: 1553-7390
- Volume/Número/Paginação/Ano: v. 7, n, 9, p. e1002278, sept. 2011
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
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: 19 abr. 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.1002278 -
NLM
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 abr. 19 ] Available from: https://doi.org/10.1371/journal.pgen.1002278 -
Vancouver
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 abr. 19 ] Available from: https://doi.org/10.1371/journal.pgen.1002278 - Craniosynostosis in pycnodysostosis: broadening the spectrum of the cranial flat bone abnormalities
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Informações sobre o DOI: 10.1371/journal.pgen.1002278 (Fonte: oaDOI API)
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