Coffin-Siris syndrome in a Brazilian child with consanguineous parents (1986)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Subjects: DOENÇAS GENÉTICAS; FAMÍLIA; MICROCEFALIA; BRASIL
- Language: Inglês
- Imprenta:
- Publisher place: Ribeirão Preto
- Date published: 1986
- Source:
- Título: Revista Brasileira de Genética
- Volume/Número/Paginação/Ano: v. 9, n. 1, p. 169-177, Mar. 1986
-
ABNT
RICHIERI-COSTA, Antonio e MONTELEONE NETO, R e GONZALES, M. L. Coffin-Siris syndrome in a Brazilian child with consanguineous parents. Revista Brasileira de Genética, v. 9, n. 1, p. 169-177, 1986Tradução . . Acesso em: 06 fev. 2026. -
APA
Richieri-Costa, A., Monteleone Neto, R., & Gonzales, M. L. (1986). Coffin-Siris syndrome in a Brazilian child with consanguineous parents. Revista Brasileira de Genética, 9( 1), 169-177. -
NLM
Richieri-Costa A, Monteleone Neto R, Gonzales ML. Coffin-Siris syndrome in a Brazilian child with consanguineous parents. Revista Brasileira de Genética. 1986 ; 9( 1): 169-177.[citado 2026 fev. 06 ] -
Vancouver
Richieri-Costa A, Monteleone Neto R, Gonzales ML. Coffin-Siris syndrome in a Brazilian child with consanguineous parents. Revista Brasileira de Genética. 1986 ; 9( 1): 169-177.[citado 2026 fev. 06 ] - 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
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas