Bertolacini, Claudia Danielli Pereira; Ribeiro-Bicudo, Lucilene Arilho 
; Petrin, A; Legnaro, Chiara de Campos; Goes, L. D; Ramalho, R; Richieri-Costa, Antonio ; Murray, Jeffrey C
Source: Abstracts. Conference titles: International Meeting on Craniofacial Anomalies: Clinical Phenotype, Genes Related and New Perspectives. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, MUTAÇÃO GENÉTICA, ANORMALIDADES CONGÊNITAS
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BERTOLACINI, Claudia Danielli Pereira et al. Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly. 2011, Anais.. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo, 2011. Disponível em: https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdf. Acesso em: 24 out. 2025.APA
Bertolacini, C. D. P., Ribeiro-Bicudo, L. A., Petrin, A., Legnaro, C. de C., Goes, L. D., Ramalho, R., et al. (2011). Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly. In Abstracts. Bauru: Hospital de Reabilitação de Anomalias Craniofaciais, Universidade de São Paulo. Recuperado de https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdfNLM
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Legnaro C de C, Goes LD, Ramalho R, Richieri-Costa A, Murray JC. Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly [Internet]. Abstracts. 2011 ;[citado 2025 out. 24 ] Available from: https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdfVancouver
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Legnaro C de C, Goes LD, Ramalho R, Richieri-Costa A, Murray JC. Duplication in splicing site of intron 2 of gene PTCH1 in seven patients with holoprosencephaly [Internet]. Abstracts. 2011 ;[citado 2025 out. 24 ] Available from: https://repositorio.usp.br/directbitstream/b433a5d9-e9ce-46e3-b97b-ae96cd6f76a9/3247647.pdf
