A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder (2012)
- Autores:
- Griesi-Oliveira, Karina
- Moreira, Danielle de Paula
- Davis-Wright, Nicole - Yale University (YALE)
- Sanders, Stephan - Yale University (YALE)
- Mason, Christopher - Yale University (YALE)
- Orabona, Guilherme Müller
- Vadasz, Estevão
- Bertola, Débora Romeo
- State, Matthew W - Yale University (YALE)
- Passos-Bueno, Maria Rita
- Autores USP: BERTOLA, DÉBORA ROMEO - IB ; BUENO, MARIA RITA DOS SANTOS E PASSOS - IB
- Unidade: IB
- DOI: 10.1002/ajmg.b.32059
- Assuntos: AUTISMO; TRANSTORNOS MENTAIS; DOENÇAS GENÉTICAS
- Idioma: Inglês
- Imprenta:
- Fonte:
- Título do periódico: American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
- ISSN: 1552-4841
- Volume/Número/Paginação/Ano: v. 159B, n. 5, p. 529-536, July 2012
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
GRIESI-OLIVEIRA, Karina et al. A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, v. 159B, n. 5, p. 529-536, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.b.32059. Acesso em: 18 abr. 2024. -
APA
Griesi-Oliveira, K., Moreira, D. de P., Davis-Wright, N., Sanders, S., Mason, C., Orabona, G. M., et al. (2012). A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 159B( 5), 529-536. doi:10.1002/ajmg.b.32059 -
NLM
Griesi-Oliveira K, Moreira D de P, Davis-Wright N, Sanders S, Mason C, Orabona GM, Vadasz E, Bertola DR, State MW, Passos-Bueno MR. A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder [Internet]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2012 ; 159B( 5): 529-536.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/ajmg.b.32059 -
Vancouver
Griesi-Oliveira K, Moreira D de P, Davis-Wright N, Sanders S, Mason C, Orabona GM, Vadasz E, Bertola DR, State MW, Passos-Bueno MR. A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder [Internet]. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2012 ; 159B( 5): 529-536.[citado 2024 abr. 18 ] Available from: https://doi.org/10.1002/ajmg.b.32059 - Craniosynostosis in pycnodysostosis: broadening the spectrum of the cranial flat bone abnormalities
- Using a combination of MLPA kits to detect chromosomal imbalances in patients with multiple congenital anomalies and mental retardation is a valuable choice for developing countries
- Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice
- Challenges in the orthodontic treatment of a patient with pycnodysostosis
- Obesity in pycnodysostosis due to UPD1: possible effect of an imprinted gene on chromosome 1
- 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
- Richieri-Costa-Pereira syndrome: expanding its phenotypicand genotypic spectrum
- An 11q11-q13.3 duplication, including FGF3 and FGF4 genes, in a patient with syndromic multiple craniosynostoses
- Unexpected role of SIX1 variants in craniosynostosis: expanding the phenotype of SIX1-related disorders
- Large deletion in PIGL: a common mutational mechanism in CHIME syndrome?
Informações sobre o DOI: 10.1002/ajmg.b.32059 (Fonte: oaDOI API)
Como citar
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
