Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? (2009)
- Authors:
- USP affiliated authors: CEIDE, ROSELI MARIA ZECHI - HRACF ; MAXIMINO, LUCIANA PAULA - FOB ; COSTA, ANTONIO RICHIERI DA - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC
- Unidades: HRACF; FOB; HRAC
- Subjects: SÍNDROME DE PIERRE ROBIN; FISSURA LÁBIOPALATINA; DISOSTOSE CRÂNIOFACIAL
- Language: Português
- Imprenta:
- Publisher: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais
- Publisher place: Bauru
- Date published: 2009
- Source:
- Título: Anais
- Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas
-
ABNT
FAVARO, F P et al. Robin sequence with cleft mandible and limb anomalies: a brazilian founder condition or an extremely rare syndrome? 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf. Acesso em: 04 out. 2024. -
APA
Favaro, F. P., Zechi-Ceide, R. M., Maximino, L. P., Antunes, L. F. P. P., 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. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf -
NLM
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFPP, 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 2024 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf -
Vancouver
Favaro FP, Zechi-Ceide RM, Maximino LP, Antunes LFPP, 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 2024 out. 04 ] Available from: https://repositorio.usp.br/directbitstream/045a13cd-5fcd-41c2-9a71-a6a5fd50d0fc/3209302.pdf - Alobar holoprosencephaly in 2 sibs: an autosomal recessive type?
- Mutação no gene EFTUD2 em um caso familial com disostose mandibulofacial tipo Guion-Almeida
- Vici's syndrome associated to cleft palate: clinical report on a brazilian boy
- Van Der Woude syndrome/popliteal pterigium syndrome: clinical and genetic variability in brazilian patients with IRF6 gene mutations
- Mandibulofacial dysostosis Bauru type Clinical genetics and radiological aspects in 13 patients: clinical genetics and radiological aspects in 13 patients
- Refinamento citogenético em indivíduos com anomalias craniofaciais sindrômicas sem diagnóstico definido
- Baraitser-Winter cerebrofrontofacial syndrome: delineation of the spectrum in 42 cases
- A compound heterozygote SLC26A2 mutation resulting in Robin Sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters: a new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasia
- Neuropsychomotor development of children aged 3 to 6 years with isolated Pierre Robin Sequence
- Disostose fronto-nasal: aspectos clínicos e genéticos
Download do texto completo
Tipo | Nome | Link | |
---|---|---|---|
3209302.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas