Phenotypic refinement of the mandibulofacial dysostosis Bauru type (2013)
- Authors:
- USP affiliated authors: COSTA, ANTONIO RICHIERI DA - HRAC ; ALMEIDA, MARIA LEINE GUION DE - HRAC ; CARREIRA, DANIELA GAMBA GARIB - FOB ; CEIDE, ROSELI MARIA ZECHI - HRAC ; MOURA, PRISCILA PADILHA - HRACF
- Unidades: HRAC; FOB; HRACF
- Subjects: DISOSTOSE MANDIBULOFACIAL; FENÓTIPOS; GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais
- Publisher place: Bauru
- Date published: 2013
- Source:
- Conference titles: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas
-
ABNT
MOURA, Priscila Padilha et al. Phenotypic refinement of the mandibulofacial dysostosis Bauru type. 2013, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2013. Disponível em: https://repositorio.usp.br/directbitstream/ffad1753-5808-49b4-9d1d-583034b0c0f4/2461351.pdf. Acesso em: 06 nov. 2024. -
APA
Moura, P. P., Richieri-Costa, A., Guion-Almeida, M. L., Garib, D. G., Yatabe, M. S., & Ceide, R. M. Z. (2013). Phenotypic refinement of the mandibulofacial dysostosis Bauru type. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/ffad1753-5808-49b4-9d1d-583034b0c0f4/2461351.pdf -
NLM
Moura PP, Richieri-Costa A, Guion-Almeida ML, Garib DG, Yatabe MS, Ceide RMZ. Phenotypic refinement of the mandibulofacial dysostosis Bauru type [Internet]. Anais. 2013 ;[citado 2024 nov. 06 ] Available from: https://repositorio.usp.br/directbitstream/ffad1753-5808-49b4-9d1d-583034b0c0f4/2461351.pdf -
Vancouver
Moura PP, Richieri-Costa A, Guion-Almeida ML, Garib DG, Yatabe MS, Ceide RMZ. Phenotypic refinement of the mandibulofacial dysostosis Bauru type [Internet]. Anais. 2013 ;[citado 2024 nov. 06 ] Available from: https://repositorio.usp.br/directbitstream/ffad1753-5808-49b4-9d1d-583034b0c0f4/2461351.pdf - 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
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