Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? (2009)
- Authors:
- USP affiliated authors: MAXIMINO, LUCIANA PAULA - FOB ; ANTUNES, LUIS FERNANDO BENEDITO BERGAMI - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; FAVARO, FRANCINE PINHEIRO - HRAC
- Unidades: FOB; HRAC
- Subjects: SÍNDROME DE PIERRE ROBIN; ANOMALIA MAXILOMANDIBULAR; FENÓTIPOS; MUTAÇÃO GENÉTICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Anais
- Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation
-
ABNT
FAVARO, Francine Pinheiro et al. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf. Acesso em: 25 fev. 2026. -
APA
Favaro, F. P., Zechi-Ceide, R. M., Maximino, L. P., Antunes, L. F. B. B., Richieri-Costa, A., & Guion-Almeida, M. L. (2009). Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf -
NLM
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFBB, Richieri-Costa A, Guion-Almeida ML. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? [Internet]. Anais. 2009 ;[citado 2026 fev. 25 ] Available from: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf -
Vancouver
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFBB, Richieri-Costa A, Guion-Almeida ML. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? [Internet]. Anais. 2009 ;[citado 2026 fev. 25 ] Available from: https://repositorio.usp.br/directbitstream/59b585bc-903b-4e7a-8bbb-b55811629da0/3100288.pdf - Richieri-Costa–Pereira syndrome: a unique acrofacial dysostosis type: an overview of the Brazilian cases
- Topic Area: genetic and Related Anomalies. Genic locus investigation in families with Richieri-Costa-Pereira Syndrome
- Newly recognized autosomal recessive MCA/MR/overgrowth syndrome
- Severe midline craniofacial anomalies: overlap with Pai syndrome
- O serviço de genética clínica no HRAC/USP
- Oral teratoma, dextrocardia, and congenital heart defect: a nonrandom association or serendipity?
- Nonsyndromic alar clefts: report of five brazilian patients
- Mental retardation, structural anomalies of the central nervous system, anophthalmia and abnormal nares: a new MCA/MR syndrome of unknown cause
- Acro-fronto-facio-nasal dysostosis: report of a new Brazilian family
- Pai syndrome: report of seven south american patients
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