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Artigo de periodico
Evaluation of genome-wide association signals for nonsyndromic cleft lip with or without cleft palate in a multiethnic Brazilian population (2022)
Machado, Renato Assis ; Rangel, Ana Lúcia Carrinho Ayrosa ; Reis, Silvia Regina de Almeida; Scariot, Rafaela ; Coletta, Ricardo Della ; Martelli Júnior, Hercílio
Fonte: Archives of Oral Biology. Unidade: HRAC
Assuntos: GENES, LÁBIO FISSURADO, FISSURA PALATINA, FISSURA LÁBIOPALATINA, FATORES DE RISCO
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ABNT
MACHADO, Renato Assis et al. Evaluation of genome-wide association signals for nonsyndromic cleft lip with or without cleft palate in a multiethnic Brazilian population. Archives of Oral Biology, v. 135, p. 6 , 2022Tradução . . Disponível em: https://doi.org/10.1016/j.archoralbio.2022.105372. Acesso em: 15 nov. 2024.
APA
Machado, R. A., Rangel, A. L. C. A., Reis, S. R. de A., Scariot, R., Coletta, R. D., & Martelli Júnior, H. (2022). Evaluation of genome-wide association signals for nonsyndromic cleft lip with or without cleft palate in a multiethnic Brazilian population. Archives of Oral Biology, 135, 6 . doi:10.1016/j.archoralbio.2022.105372
NLM
Machado RA, Rangel ALCA, Reis SR de A, Scariot R, Coletta RD, Martelli Júnior H. Evaluation of genome-wide association signals for nonsyndromic cleft lip with or without cleft palate in a multiethnic Brazilian population [Internet]. Archives of Oral Biology. 2022 ; 135 6 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.archoralbio.2022.105372
Vancouver
Machado RA, Rangel ALCA, Reis SR de A, Scariot R, Coletta RD, Martelli Júnior H. Evaluation of genome-wide association signals for nonsyndromic cleft lip with or without cleft palate in a multiethnic Brazilian population [Internet]. Archives of Oral Biology. 2022 ; 135 6 .[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.archoralbio.2022.105372
Artigo de periodico
Identification of novel variants in cleft palate-associated genes in Brazilian patients with non-syndromic cleft palate only (2021)
Machado, Renato Assis ; Martelli Júnior, Hercílio ; Reis, Silvia Regina de Almeida; Küchler, Erika Calvano ; Scariot, Rafaela ; Neves, Lucimara Teixeira das ; Coletta, Ricardo Della
Fonte: Frontiers in Cell and Developmental Biology. Unidades: FOB, HRAC
Assuntos: GENES, FISSURA PALATINA, FATORES DE RISCO, SEQUENCIAMENTO GENÉTICO
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ABNT
MACHADO, Renato Assis et al. Identification of novel variants in cleft palate-associated genes in Brazilian patients with non-syndromic cleft palate only. Frontiers in Cell and Developmental Biology, v. 9, 2021Tradução . . Disponível em: https://doi.org/10.3389/fcell.2021.638522. Acesso em: 15 nov. 2024.
APA
Machado, R. A., Martelli Júnior, H., Reis, S. R. de A., Küchler, E. C., Scariot, R., Neves, L. T. das, & Coletta, R. D. (2021). Identification of novel variants in cleft palate-associated genes in Brazilian patients with non-syndromic cleft palate only. Frontiers in Cell and Developmental Biology, 9. doi:10.3389/fcell.2021.638522
NLM
Machado RA, Martelli Júnior H, Reis SR de A, Küchler EC, Scariot R, Neves LT das, Coletta RD. Identification of novel variants in cleft palate-associated genes in Brazilian patients with non-syndromic cleft palate only [Internet]. Frontiers in Cell and Developmental Biology. 2021 ; 9[citado 2024 nov. 15 ] Available from: https://doi.org/10.3389/fcell.2021.638522
Vancouver
Machado RA, Martelli Júnior H, Reis SR de A, Küchler EC, Scariot R, Neves LT das, Coletta RD. Identification of novel variants in cleft palate-associated genes in Brazilian patients with non-syndromic cleft palate only [Internet]. Frontiers in Cell and Developmental Biology. 2021 ; 9[citado 2024 nov. 15 ] Available from: https://doi.org/10.3389/fcell.2021.638522
Artigo de periodico
Association analysis of clinical aspects and vitamin D receptor gene polymorphism with external apical root resorption in orthodontic patients (2012)
Fontana, Maria Luiza S. Simas Netta; Souza, Cleber Machado de; Bernardino, José Fabio; Hoette, Felix; Hoette, Maura Levi; Thum, Lotario; Ozawa, Terumi Okada ; Capelozza Filho, Leopoldino ; Olandoski, Marcia; Trevilatto, Paula Cristina
Fonte: American Journal of Orthodontics and Dentofacial Orthopedics. Unidades: HRAC, FOB
Assuntos: TÉCNICAS E PROCEDIMENTOS DE LABORATÓRIO, VITAMINA D, GENES, REABSORÇÃO RADICULAR, ORTODONTIA
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ABNT
FONTANA, Maria Luiza S. Simas Netta et al. Association analysis of clinical aspects and vitamin D receptor gene polymorphism with external apical root resorption in orthodontic patients. American Journal of Orthodontics and Dentofacial Orthopedics, v. 142, n. 3, p. 339-347, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.ajodo.2012.04.013. Acesso em: 15 nov. 2024.
APA
Fontana, M. L. S. S. N., Souza, C. M. de, Bernardino, J. F., Hoette, F., Hoette, M. L., Thum, L., et al. (2012). Association analysis of clinical aspects and vitamin D receptor gene polymorphism with external apical root resorption in orthodontic patients. American Journal of Orthodontics and Dentofacial Orthopedics, 142( 3), 339-347. doi:10.1016/j.ajodo.2012.04.013
NLM
Fontana MLSSN, Souza CM de, Bernardino JF, Hoette F, Hoette ML, Thum L, Ozawa TO, Capelozza Filho L, Olandoski M, Trevilatto PC. Association analysis of clinical aspects and vitamin D receptor gene polymorphism with external apical root resorption in orthodontic patients [Internet]. American Journal of Orthodontics and Dentofacial Orthopedics. 2012 ; 142( 3): 339-347.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ajodo.2012.04.013
Vancouver
Fontana MLSSN, Souza CM de, Bernardino JF, Hoette F, Hoette ML, Thum L, Ozawa TO, Capelozza Filho L, Olandoski M, Trevilatto PC. Association analysis of clinical aspects and vitamin D receptor gene polymorphism with external apical root resorption in orthodontic patients [Internet]. American Journal of Orthodontics and Dentofacial Orthopedics. 2012 ; 142( 3): 339-347.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.ajodo.2012.04.013
Artigo de periodico
Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 (2012)
Zechi-Ceide, Roseli Maria ; Rodrigues, Melina Guerreiro; Jehee, Fernanda Sarquis; Nakata, Nancy Mizue Kokitsu ; Passos-Bueno, Maria Rita ; Guion Almeida, Maria Leine
Fonte: American Journal of Medical Genetics Part A. Unidades: HRAC, IB
Assuntos: CROMOSSOMOS, GENÉTICA MÉDICA, GENES
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ABNT
ZECHI-CEIDE, Roseli Maria et al. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. American Journal of Medical Genetics Part A, v. 158A, n. 7, p. 1680\20131685, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35367. Acesso em: 15 nov. 2024.
APA
Zechi-Ceide, R. M., Rodrigues, M. G., Jehee, F. S., Nakata, N. M. K., Passos-Bueno, M. R., & Guion Almeida, M. L. (2012). Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7. American Journal of Medical Genetics Part A, 158A( 7), 1680\20131685. doi:10.1002/ajmg.a.35367
NLM
Zechi-Ceide RM, Rodrigues MG, Jehee FS, Nakata NMK, Passos-Bueno MR, Guion Almeida ML. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 [Internet]. American Journal of Medical Genetics Part A. 2012 ; 158A( 7): 1680\20131685.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.35367
Vancouver
Zechi-Ceide RM, Rodrigues MG, Jehee FS, Nakata NMK, Passos-Bueno MR, Guion Almeida ML. Saethre–Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7 [Internet]. American Journal of Medical Genetics Part A. 2012 ; 158A( 7): 1680\20131685.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.35367
Trabalho de evento-resumo
Ocular findings in a patient with a pathogenic mutation in the PTCH gene (2009)
Richieri-Costa, Antonio ; Ribeiro-Bicudo, Lucilene Arilho
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: OFTALMOLOGIA, HOLOPROSENCEFALIA, GENES
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ABNT
RICHIERI-COSTA, Antonio e RIBEIRO-BICUDO, Lucilene Arilho. Ocular findings in a patient with a pathogenic mutation in the PTCH gene. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/2f0b2631-e279-402f-8a06-da3248e9768b/3099517.pdf. Acesso em: 15 nov. 2024.
APA
Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2009). Ocular findings in a patient with a pathogenic mutation in the PTCH gene. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/2f0b2631-e279-402f-8a06-da3248e9768b/3099517.pdf
NLM
Richieri-Costa A, Ribeiro-Bicudo LA. Ocular findings in a patient with a pathogenic mutation in the PTCH gene [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/2f0b2631-e279-402f-8a06-da3248e9768b/3099517.pdf
Vancouver
Richieri-Costa A, Ribeiro-Bicudo LA. Ocular findings in a patient with a pathogenic mutation in the PTCH gene [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/2f0b2631-e279-402f-8a06-da3248e9768b/3099517.pdf
Trabalho de evento-resumo
Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate (2009)
Paula, Ligiane Alves Machado; Petrin, Aline Lourenço; Ribeiro-Bicudo, Lucilene Arilho ; Moretti Ferreira, Danilo ; Marazita, Mary L; Cooper, M. E; Mossey, Peter A; Richieri-Costa, Antonio ; Murray, Jeffrey C
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: FISSURA LÁBIOPALATINA, METABOLISMO, GENES
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ABNT
PAULA, Ligiane Alves Machado et al. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf. Acesso em: 15 nov. 2024.
APA
Paula, L. A. M., Petrin, A. L., Ribeiro-Bicudo, L. A., Moretti Ferreira, D., Marazita, M. L., Cooper, M. E., et al. (2009). Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf
NLM
Paula LAM, Petrin AL, Ribeiro-Bicudo LA, Moretti Ferreira D, Marazita ML, Cooper ME, Mossey PA, Richieri-Costa A, Murray JC. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf
Vancouver
Paula LAM, Petrin AL, Ribeiro-Bicudo LA, Moretti Ferreira D, Marazita ML, Cooper ME, Mossey PA, Richieri-Costa A, Murray JC. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/406a1218-98e4-4427-805d-1550691acd19/3099699.pdf
Trabalho de evento-resumo
Mutational analysis of TGIF and six3 genes in patients with the frontonasal dysplasia, agenesis of the corpus callosum, basal encephalocele and ocular abnormalities syndrome (2009)
Pola-Silva, L.; Richieri-Costa, Antonio ; Ribeiro-Bicudo, Lucilene Arilho
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: GENES, ANORMALIDADES CRANIOFACIAIS
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ABNT
POLA-SILVA, L. e RICHIERI-COSTA, Antonio e RIBEIRO-BICUDO, Lucilene Arilho. Mutational analysis of TGIF and six3 genes in patients with the frontonasal dysplasia, agenesis of the corpus callosum, basal encephalocele and ocular abnormalities syndrome. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/3070ceae-76f4-4f89-a6cc-a58f51202b63/3099790.pdf. Acesso em: 15 nov. 2024.
APA
Pola-Silva, L., Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2009). Mutational analysis of TGIF and six3 genes in patients with the frontonasal dysplasia, agenesis of the corpus callosum, basal encephalocele and ocular abnormalities syndrome. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/3070ceae-76f4-4f89-a6cc-a58f51202b63/3099790.pdf
NLM
Pola-Silva L, Richieri-Costa A, Ribeiro-Bicudo LA. Mutational analysis of TGIF and six3 genes in patients with the frontonasal dysplasia, agenesis of the corpus callosum, basal encephalocele and ocular abnormalities syndrome [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/3070ceae-76f4-4f89-a6cc-a58f51202b63/3099790.pdf
Vancouver
Pola-Silva L, Richieri-Costa A, Ribeiro-Bicudo LA. Mutational analysis of TGIF and six3 genes in patients with the frontonasal dysplasia, agenesis of the corpus callosum, basal encephalocele and ocular abnormalities syndrome [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/3070ceae-76f4-4f89-a6cc-a58f51202b63/3099790.pdf
Trabalho de evento-resumo
A novel heterozygous missense mutation G317D of SIX3 gene in a patient with holoprosencephaly and histiocytosis x (2009)
Ribeiro-Bicudo, Lucilene Arilho ; Richieri-Costa, Antonio
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, GENES, HISTIOCITOSE, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO-BICUDO, Lucilene Arilho e RICHIERI-COSTA, Antonio. A novel heterozygous missense mutation G317D of SIX3 gene in a patient with holoprosencephaly and histiocytosis x. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/f3e2aad0-e9c8-482c-a8b6-4489251b91a8/3099540.pdf. Acesso em: 15 nov. 2024.
APA
Ribeiro-Bicudo, L. A., & Richieri-Costa, A. (2009). A novel heterozygous missense mutation G317D of SIX3 gene in a patient with holoprosencephaly and histiocytosis x. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/f3e2aad0-e9c8-482c-a8b6-4489251b91a8/3099540.pdf
NLM
Ribeiro-Bicudo LA, Richieri-Costa A. A novel heterozygous missense mutation G317D of SIX3 gene in a patient with holoprosencephaly and histiocytosis x [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/f3e2aad0-e9c8-482c-a8b6-4489251b91a8/3099540.pdf
Vancouver
Ribeiro-Bicudo LA, Richieri-Costa A. A novel heterozygous missense mutation G317D of SIX3 gene in a patient with holoprosencephaly and histiocytosis x [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/f3e2aad0-e9c8-482c-a8b6-4489251b91a8/3099540.pdf
Trabalho de evento-resumo
Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? (2009)
Ribeiro, Lucilene Arilho ; Richieri-Costa, Antonio ; Zechi-Ceide, Roseli Maria ; Guion-Almeida, Maria Leine
Fonte: Anais. Nome do evento: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRAC, HRACF
Assuntos: HOLOPROSENCEFALIA, GÊMEOS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho et al. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/78a1506c-dcaf-41bc-bf4a-484a8be5c662/3203446.pdf. Acesso em: 15 nov. 2024.
APA
Ribeiro, L. A., Richieri-Costa, A., Zechi-Ceide, R. M., & Guion-Almeida, M. L. (2009). Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/78a1506c-dcaf-41bc-bf4a-484a8be5c662/3203446.pdf
NLM
Ribeiro LA, Richieri-Costa A, Zechi-Ceide RM, Guion-Almeida ML. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/78a1506c-dcaf-41bc-bf4a-484a8be5c662/3203446.pdf
Vancouver
Ribeiro LA, Richieri-Costa A, Zechi-Ceide RM, Guion-Almeida ML. Alobar holoprosencephaly in 2 sibs: an autosomal recessive type? [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/78a1506c-dcaf-41bc-bf4a-484a8be5c662/3203446.pdf
Trabalho de evento-resumo
Ocular findings in a patient with a pathogenic mutation in the PTCH gene (2009)
Ribeiro, Lucilene Arilho ; Richieri-Costa, Antonio
Fonte: Anais. Nome do evento: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRACF, HRAC
Assuntos: GENES, HOLOPROSENCEFALIA, OFTALMOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO, Lucilene Arilho e RICHIERI-COSTA, Antonio. Ocular findings in a patient with a pathogenic mutation in the PTCH gene. 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/2b21fd02-125c-49f0-8235-60090236bc52/3208680.pdf. Acesso em: 15 nov. 2024.
APA
Ribeiro, L. A., & Richieri-Costa, A. (2009). Ocular findings in a patient with a pathogenic mutation in the PTCH gene. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/2b21fd02-125c-49f0-8235-60090236bc52/3208680.pdf
NLM
Ribeiro LA, Richieri-Costa A. Ocular findings in a patient with a pathogenic mutation in the PTCH gene [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/2b21fd02-125c-49f0-8235-60090236bc52/3208680.pdf
Vancouver
Ribeiro LA, Richieri-Costa A. Ocular findings in a patient with a pathogenic mutation in the PTCH gene [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/2b21fd02-125c-49f0-8235-60090236bc52/3208680.pdf
Trabalho de evento-resumo
Analysis of the IRF6 and SHH genes in brazilian individuals with nonsyndromic cleft lip and palate (2009)
Bertolacini, C; Richieri-Costa, Antonio ; Ribeiro-Bicudo, Lucilene Arilho
Fonte: Anais. Nome do evento: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Assuntos: FISSURA LÁBIOPALATINA, GENES, FENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLACINI, C e RICHIERI-COSTA, Antonio e RIBEIRO-BICUDO, Lucilene Arilho. Analysis of the IRF6 and SHH genes in brazilian individuals with nonsyndromic cleft lip and palate. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/0c0c52a0-6628-4cd2-8538-300b5e7b1447/3099502.pdf. Acesso em: 15 nov. 2024.
APA
Bertolacini, C., Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2009). Analysis of the IRF6 and SHH genes in brazilian individuals with nonsyndromic cleft lip and palate. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/0c0c52a0-6628-4cd2-8538-300b5e7b1447/3099502.pdf
NLM
Bertolacini C, Richieri-Costa A, Ribeiro-Bicudo LA. Analysis of the IRF6 and SHH genes in brazilian individuals with nonsyndromic cleft lip and palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/0c0c52a0-6628-4cd2-8538-300b5e7b1447/3099502.pdf
Vancouver
Bertolacini C, Richieri-Costa A, Ribeiro-Bicudo LA. Analysis of the IRF6 and SHH genes in brazilian individuals with nonsyndromic cleft lip and palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/0c0c52a0-6628-4cd2-8538-300b5e7b1447/3099502.pdf
Trabalho de evento-resumo
Molecular analysis of the genes PTCH1 and GLI2 in brazilian individuals with ocular malformation and holoprosencephaly (2009)
Bertolacini, Claudia Danielli Pereira; Ribeiro-Bicudo, Lucilene Arilho ; Petrin, Aline Lourenço; Richieri-Costa, Antonio ; Murray, Jeffrey Clark
Fonte: Anais. Nome do evento: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidade: HRAC
Assuntos: GENÉTICA MOLECULAR, GENES, HOLOPROSENCEFALIA, OFTALMOPATIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLACINI, Claudia Danielli Pereira et al. Molecular analysis of the genes PTCH1 and GLI2 in brazilian individuals with ocular malformation and holoprosencephaly. 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/661560e3-c5c2-4838-9820-9bc6b5c9cd9b/3200602.pdf. Acesso em: 15 nov. 2024.
APA
Bertolacini, C. D. P., Ribeiro-Bicudo, L. A., Petrin, A. L., Richieri-Costa, A., & Murray, J. C. (2009). Molecular analysis of the genes PTCH1 and GLI2 in brazilian individuals with ocular malformation and holoprosencephaly. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/661560e3-c5c2-4838-9820-9bc6b5c9cd9b/3200602.pdf
NLM
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin AL, Richieri-Costa A, Murray JC. Molecular analysis of the genes PTCH1 and GLI2 in brazilian individuals with ocular malformation and holoprosencephaly [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/661560e3-c5c2-4838-9820-9bc6b5c9cd9b/3200602.pdf
Vancouver
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin AL, Richieri-Costa A, Murray JC. Molecular analysis of the genes PTCH1 and GLI2 in brazilian individuals with ocular malformation and holoprosencephaly [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/661560e3-c5c2-4838-9820-9bc6b5c9cd9b/3200602.pdf
Trabalho de evento-resumo
Analysis of the IRF6 and SHH genes in brazilian individuals with nosnsyndromic cleft lip and palate (2009)
Bertolacini, Claudia Danielli Pereira; Richieri-Costa, Antonio ; Ribeiro-Bicudo, Lucilene Arilho
Fonte: Anais. Nome do evento: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidade: HRAC
Assuntos: FISSURA LÁBIOPALATINA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLACINI, Claudia Danielli Pereira e RICHIERI-COSTA, Antonio e RIBEIRO-BICUDO, Lucilene Arilho. Analysis of the IRF6 and SHH genes in brazilian individuals with nosnsyndromic cleft lip and palate. 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/bca3ae75-17bd-48f0-a820-993207b0e5fa/3203519.pdf. Acesso em: 15 nov. 2024.
APA
Bertolacini, C. D. P., Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2009). Analysis of the IRF6 and SHH genes in brazilian individuals with nosnsyndromic cleft lip and palate. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/bca3ae75-17bd-48f0-a820-993207b0e5fa/3203519.pdf
NLM
Bertolacini CDP, Richieri-Costa A, Ribeiro-Bicudo LA. Analysis of the IRF6 and SHH genes in brazilian individuals with nosnsyndromic cleft lip and palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/bca3ae75-17bd-48f0-a820-993207b0e5fa/3203519.pdf
Vancouver
Bertolacini CDP, Richieri-Costa A, Ribeiro-Bicudo LA. Analysis of the IRF6 and SHH genes in brazilian individuals with nosnsyndromic cleft lip and palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/bca3ae75-17bd-48f0-a820-993207b0e5fa/3203519.pdf
Trabalho de evento-resumo
Mutation in gas1 gene in individuals with holoprosencephalia-like phenotype (2009)
Nascimento, A; Quiezi, Rodrigo Gonçalves; Ferreira, A. P; Goes, L. D; Richieri-Costa, Antonio ; Ribeiro-Bicudo, Lucilene Arilho
Fonte: Anais. Nome do evento: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, FENÓTIPOS, MUTAÇÃO GENÉTICA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
NASCIMENTO, A et al. Mutation in gas1 gene in individuals with holoprosencephalia-like phenotype. 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/5675df6c-efbe-4c2b-9080-6744f238cf67/3203398.pdf. Acesso em: 15 nov. 2024.
APA
Nascimento, A., Quiezi, R. G., Ferreira, A. P., Goes, L. D., Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2009). Mutation in gas1 gene in individuals with holoprosencephalia-like phenotype. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/5675df6c-efbe-4c2b-9080-6744f238cf67/3203398.pdf
NLM
Nascimento A, Quiezi RG, Ferreira AP, Goes LD, Richieri-Costa A, Ribeiro-Bicudo LA. Mutation in gas1 gene in individuals with holoprosencephalia-like phenotype [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/5675df6c-efbe-4c2b-9080-6744f238cf67/3203398.pdf
Vancouver
Nascimento A, Quiezi RG, Ferreira AP, Goes LD, Richieri-Costa A, Ribeiro-Bicudo LA. Mutation in gas1 gene in individuals with holoprosencephalia-like phenotype [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/5675df6c-efbe-4c2b-9080-6744f238cf67/3203398.pdf
Artigo de periodico
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes (2009)
Zechi-Ceide, Roseli Maria; Ribeiro, Lucilene Arilho; Raskin, Salmo; Bertolacini, Claudia Danielli Pereira; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Fonte: American Journal of Medical Genetics. Part A. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, FISSURA LÁBIOPALATINA BILATERAL, GENES, ANORMALIDADES MÚLTIPLAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ZECHI-CEIDE, Roseli Maria et al. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics. Part A, v. 149A, n. 6, p. 1277-1279, 2009Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.32844. Acesso em: 15 nov. 2024.
APA
Zechi-Ceide, R. M., Ribeiro, L. A., Raskin, S., Bertolacini, C. D. P., Guion-Almeida, M. L., & Richieri-Costa, A. (2009). Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes. American Journal of Medical Genetics. Part A, 149A( 6), 1277-1279. doi:10.1002/ajmg.a.32844
NLM
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CDP, Guion-Almeida ML, Richieri-Costa A. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1277-1279.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.32844
Vancouver
Zechi-Ceide RM, Ribeiro LA, Raskin S, Bertolacini CDP, Guion-Almeida ML, Richieri-Costa A. Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genes [Internet]. American Journal of Medical Genetics. Part A. 2009 ; 149A( 6): 1277-1279.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1002/ajmg.a.32844
Trabalho de evento-resumo
Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate (2009)
Machado-Paula, Ligiane Alves ; Petrin, Aline Lourenço; Ribeiro-Bicudo, Lucilene Arilho ; Moretti Ferreira, Danilo ; Marazita, M. L; Cooper, M. E; Mossey, Peter Anthony ; Richieri-Costa, Antonio ; Murray, Jeffrey Clark
Fonte: Anais. Nome do evento: Simpósio Internacional de Fissuras Orofaciais e Anomalias Relacionadas. Unidades: HRACF, HRAC
Assuntos: ÁCIDO FÓLICO, FISSURA LÁBIOPALATINA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MACHADO-PAULA, Ligiane Alves et al. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate. 2009, Anais.. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais, 2009. Disponível em: https://repositorio.usp.br/directbitstream/c70a45af-3cf6-43bd-9d1e-4d65a50755a9/3207263.pdf. Acesso em: 15 nov. 2024.
APA
Machado-Paula, L. A., Petrin, A. L., Ribeiro-Bicudo, L. A., Moretti Ferreira, D., Marazita, M. L., Cooper, M. E., et al. (2009). Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate. In Anais. Bauru: Universidade de São Paulo, Hospital de Reabilitação de Anomalias Craniofaciais. Recuperado de https://repositorio.usp.br/directbitstream/c70a45af-3cf6-43bd-9d1e-4d65a50755a9/3207263.pdf
NLM
Machado-Paula LA, Petrin AL, Ribeiro-Bicudo LA, Moretti Ferreira D, Marazita ML, Cooper ME, Mossey PA, Richieri-Costa A, Murray JC. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/c70a45af-3cf6-43bd-9d1e-4d65a50755a9/3207263.pdf
Vancouver
Machado-Paula LA, Petrin AL, Ribeiro-Bicudo LA, Moretti Ferreira D, Marazita ML, Cooper ME, Mossey PA, Richieri-Costa A, Murray JC. Association of folate metabolism genes with brazilian cases of nonsyndromic cleft lip and/or palate [Internet]. Anais. 2009 ;[citado 2024 nov. 15 ] Available from: https://repositorio.usp.br/directbitstream/c70a45af-3cf6-43bd-9d1e-4d65a50755a9/3207263.pdf
Artigo de periodico
Variable phenotypic manifestations of a K44N mutation in the TGIF gene (2008)
Richieri-Costa, Antonio; Ribeiro, Lucilene Arilho
Fonte: Brain & Development. Unidade: HRAC
Assuntos: HOLOPROSENCEFALIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHIERI-COSTA, Antonio e RIBEIRO, Lucilene Arilho. Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, v. 30, n. 3, p. 203-205, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.braindev.2007.07.012. Acesso em: 15 nov. 2024.
APA
Richieri-Costa, A., & Ribeiro, L. A. (2008). Variable phenotypic manifestations of a K44N mutation in the TGIF gene. Brain & Development, 30( 3), 203-205. doi:10.1016/j.braindev.2007.07.012
NLM
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.braindev.2007.07.012
Vancouver
Richieri-Costa A, Ribeiro LA. Variable phenotypic manifestations of a K44N mutation in the TGIF gene [Internet]. Brain & Development. 2008 ; 30( 3): 203-205.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1016/j.braindev.2007.07.012
Artigo de periodico
Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene (2008)
Ceide, Roseli Maria Zechi; Oliveira, Nélio Alessandro de Jesus; Guion-Almeida, Maria Leine; Antunes, Luis Fernando Benedito Bergami; Richieri-Costa, Antonio; Passos-Bueno, Maria Rita
Fonte: Clinical Dysmorphology. Unidades: HRAC, IB
Assuntos: ANORMALIDADES MÚLTIPLAS, FENÓTIPOS, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CEIDE, Roseli Maria Zechi et al. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, v. 17, n. 3, p. 225-226, 2008Tradução . . Disponível em: https://doi.org/10.1097/mcd.0b013e3282fe1b8e. Acesso em: 15 nov. 2024.
APA
Ceide, R. M. Z., Oliveira, N. A. de J., Guion-Almeida, M. L., Antunes, L. F. B. B., Richieri-Costa, A., & Passos-Bueno, M. R. (2008). Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene. Clinical Dysmorphology, 17( 3), 225-226. doi:10.1097/mcd.0b013e3282fe1b8e
NLM
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Vancouver
Ceide RMZ, Oliveira NA de J, Guion-Almeida ML, Antunes LFBB, Richieri-Costa A, Passos-Bueno MR. Unusual phenotype in a female patient with a Gly25Ala substitution in the signal peptide region of the COL2A1 gene [Internet]. Clinical Dysmorphology. 2008 ; 17( 3): 225-226.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1097/mcd.0b013e3282fe1b8e
Artigo de periodico
Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study (2004)
Passos-Bueno, Maria Rita ; Gaspar, Dinamar A.; Kamiya, Tânia Yoshico; Tescarollo, Graziela; Rabanéa, Daniel Saraiva; Richieri-Costa, Antonio; Alonso, Nivaldo; Araújo, Belmino
Fonte: The Cleft Palate-Craniofacial Journal. Unidades: IB, HRAC
Assuntos: GENES, FISSURA LÁBIOPALATINA, GENÓTIPOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PASSOS-BUENO, Maria Rita et al. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, v. 41, n. 4, p. 387-391, 2004Tradução . . Acesso em: 15 nov. 2024.
APA
Passos-Bueno, M. R., Gaspar, D. A., Kamiya, T. Y., Tescarollo, G., Rabanéa, D. S., Richieri-Costa, A., et al. (2004). Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal, 41( 4), 387-391.
NLM
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 nov. 15 ]
Vancouver
Passos-Bueno MR, Gaspar DA, Kamiya TY, Tescarollo G, Rabanéa DS, Richieri-Costa A, Alonso N, Araújo B. Transforming growth factor-alpha and nonsyndromic cleft lip with or without palate in brazilian patients: results of a large case-control study. The Cleft Palate-Craniofacial Journal. 2004 ; 41( 4): 387-391.[citado 2024 nov. 15 ]
Artigo de periodico
Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia (2000)
Suzuki, Koji; Hu, Diane; Bustos, Tania; Zlotogora, Joel; Richieri-Costa, Antonio; Helms, Jill A.; Spritz, Richard A.
Fonte: Nature Genetics. Unidade: HRAC
Assuntos: MUTAÇÃO GENÉTICA, GENES, FISSURA LÁBIOPALATINA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SUZUKI, Koji et al. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nature Genetics, v. 25, p. 427-430, 2000Tradução . . Disponível em: https://doi.org/10.1038/78119. Acesso em: 15 nov. 2024.
APA
Suzuki, K., Hu, D., Bustos, T., Zlotogora, J., Richieri-Costa, A., Helms, J. A., & Spritz, R. A. (2000). Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia. Nature Genetics, 25, 427-430. doi:10.1038/78119
NLM
Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia [Internet]. Nature Genetics. 2000 ; 25 427-430.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/78119
Vancouver
Suzuki K, Hu D, Bustos T, Zlotogora J, Richieri-Costa A, Helms JA, Spritz RA. Mutations of PVRL1, encoding a cell-cell adhesion molecule/herpesvirus receptor, in cleft lip/palate-ectodermal dysplasia [Internet]. Nature Genetics. 2000 ; 25 427-430.[citado 2024 nov. 15 ] Available from: https://doi.org/10.1038/78119

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