Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome (2011)
- Authors:
- USP affiliated authors: COSTA, SILVIA SOUZA DA - IB ; BERTOLA, DÉBORA ROMEO - IB ; MORGANTE, ANGELA MARIA VIANNA - IB
- Unidade: IB
- DOI: 10.1002/ajmg.a.34023
- Subjects: DOENÇAS GENÉTICAS; EXPRESSÃO GÊNICA; ANORMALIDADES CROMOSSÔMICAS
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: American Journal of Medical Genetics Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 155, n. 10, p. 2479-2483, Oct. 2011
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
BONALDI, Adriano et al. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome. American Journal of Medical Genetics Part A, v. 155, n. 10, p. 2479-2483, 2011Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.34023. Acesso em: 19 abr. 2024. -
APA
Bonaldi, A., Mazzeu, J. F., Costa, S. S. da, Honjo, R. S., Bertola, D. R., Albano, L. M. J., et al. (2011). Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome. American Journal of Medical Genetics Part A, 155( 10), 2479-2483. doi:10.1002/ajmg.a.34023 -
NLM
Bonaldi A, Mazzeu JF, Costa SS da, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Vianna-Morgante AM. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome [Internet]. American Journal of Medical Genetics Part A. 2011 ; 155( 10): 2479-2483.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.34023 -
Vancouver
Bonaldi A, Mazzeu JF, Costa SS da, Honjo RS, Bertola DR, Albano LMJ, Furquim IM, Kim CA, Vianna-Morgante AM. Microduplication of the ICR2 domain at chromosome 11p15 and familial Silver–Russell syndrome [Internet]. American Journal of Medical Genetics Part A. 2011 ; 155( 10): 2479-2483.[citado 2024 abr. 19 ] Available from: https://doi.org/10.1002/ajmg.a.34023 - PLP1 duplication at the breakpoint regions of an apparently balanced t(X,22) translocation causes Pelizaeus-Merzbacher disease in a girl
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Informações sobre o DOI: 10.1002/ajmg.a.34023 (Fonte: oaDOI API)
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