An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses (2007)
- Authors:
- USP affiliated authors: BERTOLA, DÉBORA ROMEO - IB ; MORGANTE, ANGELA MARIA VIANNA - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidade: IB
- DOI: 10.1002/ajmg.a.31863
- Subjects: CRANIOSSINOSTOSE; ANORMALIDADES CROMOSSÔMICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 143A, n. 16, p. 1912-1918, 2007
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
JEHEE, Fernanda Sarquis et al. An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses. American Journal of Medical Genetics. Part A, v. 143A, n. 16, p. 1912-1918, 2007Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.31863. Acesso em: 24 abr. 2024. -
APA
Jehee, F. S., Bertola, D. R., Yelavarthi, K. K., Krepischi, A. C. V., Kim, C., Vianna-Morgante, A. M., et al. (2007). An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses. American Journal of Medical Genetics. Part A, 143A( 16), 1912-1918. doi:10.1002/ajmg.a.31863 -
NLM
Jehee FS, Bertola DR, Yelavarthi KK, Krepischi ACV, Kim C, Vianna-Morgante AM, Vermeesch JR, Passos-Bueno MR. An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 16): 1912-1918.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1002/ajmg.a.31863 -
Vancouver
Jehee FS, Bertola DR, Yelavarthi KK, Krepischi ACV, Kim C, Vianna-Morgante AM, Vermeesch JR, Passos-Bueno MR. An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses [Internet]. American Journal of Medical Genetics. Part A. 2007 ; 143A( 16): 1912-1918.[citado 2024 abr. 24 ] Available from: https://doi.org/10.1002/ajmg.a.31863 - High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation
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Informações sobre o DOI: 10.1002/ajmg.a.31863 (Fonte: oaDOI API)
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