Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum (2011)
- Authors:
- USP affiliated authors: NAKATA, NANCY MIZUE KOKITSU - HRAC ; BICUDO, LUCILENE ARILHO RIBEIRO - HRAC ; COSTA, ANTONIO RICHIERI DA - HRAC ; PITTOLI, SIULAN VENDRAMINI PAULOVICH - HRAC
- Unidade: HRAC
- Subjects: ANORMALIDADES MÚLTIPLAS; ANORMALIDADES CROMOSSÔMICAS; GENÉTICA
- Language: Inglês
- Imprenta:
- Publisher: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo
- Publisher place: Bauru
- Date published: 2011
- Source:
- Título: Abstracts
- Conference titles: International Meeting on Craniofacial Anomalies: Clinical Phenotype, Genes Related and New Perspectives
-
ABNT
MACHADO-PAULA, Ligiane Alves et al. Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum. 2011, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2011. Disponível em: https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf. Acesso em: 28 dez. 2025. -
APA
Machado-Paula, L. A., Vendramini-Pittoli, S., Kokitsu-Nakata, N. M., Ribeiro-Bicudo, L. A., Richieri-Costa, A., & Murray, J. C. (2011). Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum. In Abstracts. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf -
NLM
Machado-Paula LA, Vendramini-Pittoli S, Kokitsu-Nakata NM, Ribeiro-Bicudo LA, Richieri-Costa A, Murray JC. Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum [Internet]. Abstracts. 2011 ;[citado 2025 dez. 28 ] Available from: https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf -
Vancouver
Machado-Paula LA, Vendramini-Pittoli S, Kokitsu-Nakata NM, Ribeiro-Bicudo LA, Richieri-Costa A, Murray JC. Microarray analysis in Brazilian patients with the oculoauriculovertebral spectrum [Internet]. Abstracts. 2011 ;[citado 2025 dez. 28 ] Available from: https://repositorio.usp.br/directbitstream/6007ea78-c39b-4a8e-b5a0-ce7cd5632b4f/3247768.pdf - Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
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