Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects (2005)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- DOI: 10.1002/ajmg.a.30627
- Subjects: ANORMALIDADES MÚLTIPLAS; HOLOPROSENCEFALIA; FISSURA LÁBIOPALATINA
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics. Part A
- ISSN: 1552-4825
- Volume/Número/Paginação/Ano: v. 136, n. 4, p. 350-351, Aug., 2005
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
RIBEIRO, Lucilene Arilho e GUERINI, Rita de Cássia Mecca e RICHIERI-COSTA, Antonio. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, v. 136, n. 4, p. 350-351, 2005Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.30627. Acesso em: 06 fev. 2026. -
APA
Ribeiro, L. A., Guerini, R. de C. M., & Richieri-Costa, A. (2005). Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects. American Journal of Medical Genetics. Part A, 136( 4), 350-351. doi:10.1002/ajmg.a.30627 -
NLM
Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2026 fev. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30627 -
Vancouver
Ribeiro LA, Guerini R de CM, Richieri-Costa A. Holoprosencephaly with microphthalmia, hypoplastic ears, vertebral segmentation defects, and congenital heart defects [Internet]. American Journal of Medical Genetics. Part A. 2005 ; 136( 4): 350-351.[citado 2026 fev. 06 ] Available from: https://doi.org/10.1002/ajmg.a.30627 - 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
- 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
- Coffin-Siris syndrome in a Brazilian child with consanguineous parents
Informações sobre o DOI: 10.1002/ajmg.a.30627 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
