Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients (1992)
- Authors:
- Autor USP: COSTA, ANTONIO RICHIERI DA - HRAC
- Unidade: HRAC
- Assunto: SÍNDROME DE GOLDENHAR
- Language: Inglês
- Imprenta:
- Source:
- Título: American Journal of Medical Genetics
- Volume/Número/Paginação/Ano: v. 44, n. 5, p. 683-690, Nov. 1992
-
ABNT
BEVER, Yolande van e ENDE, Jenny J. van den e RICHIERI-COSTA, Antonio. Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients. American Journal of Medical Genetics, v. No 1992, n. 5, p. 683-690, 1992Tradução . . Acesso em: 29 dez. 2025. -
APA
Bever, Y. van, Ende, J. J. van den, & Richieri-Costa, A. (1992). Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients. American Journal of Medical Genetics, No 1992( 5), 683-690. -
NLM
Bever Y van, Ende JJ van den, Richieri-Costa A. Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients. American Journal of Medical Genetics. 1992 ; No 1992( 5): 683-690.[citado 2025 dez. 29 ] -
Vancouver
Bever Y van, Ende JJ van den, Richieri-Costa A. Oculo-auriculo-vertebral complex and uncommon associated anomalies: report on 8 unrelated Brazilian patients. American Journal of Medical Genetics. 1992 ; No 1992( 5): 683-690.[citado 2025 dez. 29 ] - Branchio-oto-renal (BOR) syndrome: report of a brazilian family
- Genotype-phenotype correlation in two patients with familiar Pfeiffer syndrome
- A década da linguagem - os genes começam a falar
- Macrostomia, preauricular tags, and external ophthalmoplegia: a new autosomal dominant syndrome within the oculoauriculovertebral spectrum?
- Oblique facial clefts: report on 4 Brazilian patients. Evidence for clinical variability and genetic heterogeneity
- Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) and cleft lip and palate. Report of two Brazilian families
- A study of familial stuttering
- SIX3 mutations with holoprosencephaly
- Autosomal recessive blepharoptosis, cleft lip/palate, dental anomalies, and ectrodactyly
- Holoprosencephaly and holoprosencephaly-like phenotypes: review of facial and molecular findings in patients from a craniofacial hospital in Brazil
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas