Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases (2005)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.a.30628
- Subjects: ANORMALIDADES MÚLTIPLAS; HOLOPROSENCEFALIA
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 136, n. 4, p. 352-353, Aug., 2005
- Este artigo NÃO possui versão em acesso aberto
-
Status: Nenhuma versão em acesso aberto identificada -
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 352-353, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30628. Acesso em: 13 mar. 2026. -
APA
Richieri-Costa, A., & Ribeiro, L. A. (2005). Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases. American Journal of Medical Genetics. Part A, 136( 4), 352-353. doi:10.1002/ajmg.a.30628 -
NLM
Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2026 mar. 13 ] Available from: https://doi.org/10.1002/ajmg.a.30628 -
Vancouver
Richieri-Costa A, Ribeiro LA. Cerebro-oculo-nasal syndrome, a disorder with some manifestations suggestive of the holoprosencephalic spectrum: new case and imaging review of previous cases [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 352-353.[citado 2026 mar. 13 ] Available from: https://doi.org/10.1002/ajmg.a.30628 - Noonan syndrome in diverse populations
- Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?
- Ulnar ray a/hypoplasia: evidence for a developmental field defect on the basis of genetic heterogeneity. Report of three Brazilian families
- Acheiropodia: report on four new Brazilian patients
- Van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures
- Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects
- Syndrome of acrofacial dysostosis, cleft lip/palate, and triphalangeal thumb in a Brazilian family [Brief clinical report]
- Turner syndrome in diverse populations
- Coloboma treatment in Treacher Collins syndrome personal contributions
- Cerebro-oculo-nasal syndrome: report of a case with a severe phenotype
Informações sobre a disponibilidade de versões do artigo em acesso aberto coletadas automaticamente via oaDOI API (Unpaywall).
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
