ReP USP - Resultado da busca

Artigo de periodico
Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 (2020)
Pittoli, Siulan Vendramini Paulovich ; Souza, Rosana Maria Candido ; Quiezi, Rodrigo Gonçalves; Zechi-Ceide, Roseli Maria ; Nakata, Nancy Mizue Kokitsu ; Jehee, Fernanda Sarquis; Ribeiro-Bicudo, Lucilene Arilho ; FitzPatrick, David R. ; Guion-Almeida, Maria Leine; Richieri-Costa, Antonio
Source: Journal of Pediatric Genetics. Unidades: HRAC, HRACF
Subjects: AGENESIA, FISSURA PALATINA, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PITTOLI, Siulan Vendramini Paulovich et al. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, v. 9, n. 4, p. 258-262, 2020Tradução . . Disponível em: https://doi.org/10.1055/s-0039-3402047. Acesso em: 23 maio 2024.
APA
Pittoli, S. V. P., Souza, R. M. C., Quiezi, R. G., Zechi-Ceide, R. M., Nakata, N. M. K., Jehee, F. S., et al. (2020). Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2. Journal of Pediatric Genetics, 9( 4), 258-262. doi:10.1055/s-0039-3402047
NLM
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 maio 23 ] Available from: https://doi.org/10.1055/s-0039-3402047
Vancouver
Pittoli SVP, Souza RMC, Quiezi RG, Zechi-Ceide RM, Nakata NMK, Jehee FS, Ribeiro-Bicudo LA, FitzPatrick DR, Guion-Almeida ML, Richieri-Costa A. Microphthalmia, linear skin defects, callosal agenesis, and cleft palate in a patient with deletion at Xp22.3p22.2 [Internet]. Journal of Pediatric Genetics. 2020 ; 9( 4): 258-262.[citado 2024 maio 23 ] Available from: https://doi.org/10.1055/s-0039-3402047
Artigo de periodico
Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability (2016)
Gamba, Bruno Faulin; Zechi-Ceide, Roseli Maria; Kokitsu-Nakata, Nancy Mizue; Vendramini-Pittoli, Siulan; Rosenberg, Carla ; Santos, Ana Carolina Alves dos; Ribeiro-Bicudo, Lucilene Arilho; Richieri-Costa, Antonio
Source: Molecular Syndromology. Unidades: HRAC, IB
Subjects: ANORMALIDADES CONGÊNITAS, MICROCEFALIA, DEFICIÊNCIA MENTAL, DELEÇÃO DE GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GAMBA, Bruno Faulin et al. Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability. Molecular Syndromology, v. 7, n. 6, p. 344-348, 2016Tradução . . Disponível em: https://doi.org/10.1159/000450971. Acesso em: 23 maio 2024.
APA
Gamba, B. F., Zechi-Ceide, R. M., Kokitsu-Nakata, N. M., Vendramini-Pittoli, S., Rosenberg, C., Santos, A. C. A. dos, et al. (2016). Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability. Molecular Syndromology, 7( 6), 344-348. doi:10.1159/000450971
NLM
Gamba BF, Zechi-Ceide RM, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Santos ACA dos, Ribeiro-Bicudo LA, Richieri-Costa A. Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability [Internet]. Molecular Syndromology. 2016 ; 7( 6): 344-348.[citado 2024 maio 23 ] Available from: https://doi.org/10.1159/000450971
Vancouver
Gamba BF, Zechi-Ceide RM, Kokitsu-Nakata NM, Vendramini-Pittoli S, Rosenberg C, Santos ACA dos, Ribeiro-Bicudo LA, Richieri-Costa A. Interstitial 1q21.1 microdeletion is associated with severe skeletal anomalies, dysmorphic face and moderate intellectual disability [Internet]. Molecular Syndromology. 2016 ; 7( 6): 344-348.[citado 2024 maio 23 ] Available from: https://doi.org/10.1159/000450971
Artigo de periodico
Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies (2015)
Gamba, Bruno Faulin; Richieri-Costa, Antonio ; Costa, Silvia; Rosenberg, Carla ; Ribeiro-Bicudo, Lucilene Arilho
Source: Molecular Genetics and Genomics. Unidades: HRAC, IB
Subjects: DOENÇAS GENÉTICAS, CROMOSSOMOS HUMANOS (ANOMALIAS), MALFORMAÇÕES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GAMBA, Bruno Faulin et al. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, n. Ju 2015, p. on-line, 2015Tradução . . Disponível em: https://doi.org/10.1007/s00438-015-1072-0. Acesso em: 23 maio 2024.
APA
Gamba, B. F., Richieri-Costa, A., Costa, S., Rosenberg, C., & Ribeiro-Bicudo, L. A. (2015). Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies. Molecular Genetics and Genomics, ( Ju 2015), on-line. doi:10.1007/s00438-015-1072-0
NLM
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 maio 23 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
Vancouver
Gamba BF, Richieri-Costa A, Costa S, Rosenberg C, Ribeiro-Bicudo LA. Chromothripsis with at least 12 breaks at 1p36.33-p35.3 in a boy with multiple congenital anomalies [Internet]. Molecular Genetics and Genomics. 2015 ;( Ju 2015): on-line.[citado 2024 maio 23 ] Available from: https://doi.org/10.1007/s00438-015-1072-0
Artigo de periodico
Clinical findings in patients with GLI2 mutations: phenotypic variability (2012)
Bertolacini, Claudia Danielli Pereira; Ribeiro-Bicudo, Lucilene Arilho ; Petrin, A.; Richieri-Costa, Antonio ; Murray, Jeffrey C
Source: Clinical Genetics. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, ANORMALIDADES CRANIOFACIAIS, MUTAÇÃO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLACINI, Claudia Danielli Pereira et al. Clinical findings in patients with GLI2 mutations: phenotypic variability. Clinical Genetics, v. 81, n. Ja 2012, p. 70-75, 2012Tradução . . Disponível em: https://doi.org/10.1111/j.1399-0004.2010.01606.x. Acesso em: 23 maio 2024.
APA
Bertolacini, C. D. P., Ribeiro-Bicudo, L. A., Petrin, A., Richieri-Costa, A., & Murray, J. C. (2012). Clinical findings in patients with GLI2 mutations: phenotypic variability. Clinical Genetics, 81( Ja 2012), 70-75. doi:10.1111/j.1399-0004.2010.01606.x
NLM
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Clinical findings in patients with GLI2 mutations: phenotypic variability [Internet]. Clinical Genetics. 2012 ; 81( Ja 2012): 70-75.[citado 2024 maio 23 ] Available from: https://doi.org/10.1111/j.1399-0004.2010.01606.x
Vancouver
Bertolacini CDP, Ribeiro-Bicudo LA, Petrin A, Richieri-Costa A, Murray JC. Clinical findings in patients with GLI2 mutations: phenotypic variability [Internet]. Clinical Genetics. 2012 ; 81( Ja 2012): 70-75.[citado 2024 maio 23 ] Available from: https://doi.org/10.1111/j.1399-0004.2010.01606.x
Artigo de periodico
Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies (2012)
Ribeiro-Bicudo, Lucilene Arilho ; Quiezi, Rodrigo Gonçalves; Guion-Almeida, Maria Leine; Legnaro, Chiara; Richieri-Costa, Antonio
Source: American Journal of Medical Genetics, Part A. Unidade: HRAC
Subjects: ANORMALIDADES CRANIOFACIAIS, SÍNDROMES OROFACIODIGITAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RIBEIRO-BICUDO, Lucilene Arilho et al. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies. American Journal of Medical Genetics, Part A, v. 158A, n. 5, p. 1233-1235, 2012Tradução . . Disponível em: https://doi.org/10.1002/ajmg.a.35305. Acesso em: 23 maio 2024.
APA
Ribeiro-Bicudo, L. A., Quiezi, R. G., Guion-Almeida, M. L., Legnaro, C., & Richieri-Costa, A. (2012). Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies. American Journal of Medical Genetics, Part A, 158A( 5), 1233-1235. doi:10.1002/ajmg.a.35305
NLM
Ribeiro-Bicudo LA, Quiezi RG, Guion-Almeida ML, Legnaro C, Richieri-Costa A. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies [Internet]. American Journal of Medical Genetics, Part A. 2012 ; 158A( 5): 1233-1235.[citado 2024 maio 23 ] Available from: https://doi.org/10.1002/ajmg.a.35305
Vancouver
Ribeiro-Bicudo LA, Quiezi RG, Guion-Almeida ML, Legnaro C, Richieri-Costa A. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies [Internet]. American Journal of Medical Genetics, Part A. 2012 ; 158A( 5): 1233-1235.[citado 2024 maio 23 ] Available from: https://doi.org/10.1002/ajmg.a.35305
Artigo de periodico
Quality evaluation of DNA obtained from stored human saliva and its applicability to identification in Forensic Dentistry (2010)
Carvalho, Suzana Papile Maciel; Sales-Peres, Arsenio; Ribeiro-Bicudo, Lucilene Arilho; Silva, Ricardo Henrique Alves da
Source: Revista Odonto Ciência. Unidade: FORP
Subjects: ODONTOLOGIA LEGAL, SALIVA, DNA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Suzana Papile Maciel et al. Quality evaluation of DNA obtained from stored human saliva and its applicability to identification in Forensic Dentistry. Revista Odonto Ciência, v. 25, n. 1, p. 48-53, 2010Tradução . . Disponível em: https://doi.org/10.1590/s1980-65232010000100010. Acesso em: 23 maio 2024.
APA
Carvalho, S. P. M., Sales-Peres, A., Ribeiro-Bicudo, L. A., & Silva, R. H. A. da. (2010). Quality evaluation of DNA obtained from stored human saliva and its applicability to identification in Forensic Dentistry. Revista Odonto Ciência, 25( 1), 48-53. doi:10.1590/s1980-65232010000100010
NLM
Carvalho SPM, Sales-Peres A, Ribeiro-Bicudo LA, Silva RHA da. Quality evaluation of DNA obtained from stored human saliva and its applicability to identification in Forensic Dentistry [Internet]. Revista Odonto Ciência. 2010 ; 25( 1): 48-53.[citado 2024 maio 23 ] Available from: https://doi.org/10.1590/s1980-65232010000100010
Vancouver
Carvalho SPM, Sales-Peres A, Ribeiro-Bicudo LA, Silva RHA da. Quality evaluation of DNA obtained from stored human saliva and its applicability to identification in Forensic Dentistry [Internet]. Revista Odonto Ciência. 2010 ; 25( 1): 48-53.[citado 2024 maio 23 ] Available from: https://doi.org/10.1590/s1980-65232010000100010
Artigo de periodico
Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly (2010)
Bertolacini, Claudia Danielli Pereira; Richieri-Costa, Antonio; Ribeiro-Bicudo, Lucilene Arilho
Source: Brain & Development. Unidade: HRAC
Subjects: MUTAÇÃO GENÉTICA, POLIMORFISMO, HOLOPROSENCEFALIA
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. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly. Brain & Development, v. 32, n. 3, p. 217-222, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.braindev.2009.02.014. Acesso em: 23 maio 2024.
APA
Bertolacini, C. D. P., Richieri-Costa, A., & Ribeiro-Bicudo, L. A. (2010). Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly. Brain & Development, 32( 3), 217-222. doi:10.1016/j.braindev.2009.02.014
NLM
Bertolacini CDP, Richieri-Costa A, Ribeiro-Bicudo LA. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly [Internet]. Brain & Development. 2010 ; 32( 3): 217-222.[citado 2024 maio 23 ] Available from: https://doi.org/10.1016/j.braindev.2009.02.014
Vancouver
Bertolacini CDP, Richieri-Costa A, Ribeiro-Bicudo LA. Sonic hedgehog (SHH) mutation in patients within the spectrum of holoprosencephaly [Internet]. Brain & Development. 2010 ; 32( 3): 217-222.[citado 2024 maio 23 ] Available from: https://doi.org/10.1016/j.braindev.2009.02.014
Artigo de periodico
Avaliação da qualidade do DNA extraído de saliva humana armazenada e sua aplicabilidade na identificação em Odontologia Legal (2010)
Carvalho, Suzana Papile Maciel; Sales-Peres, Arsenio; Ribeiro-Bicudo, Lucilene Arilho; Silva, Ricardo Henrique Alves da
Source: Revista Odonto Ciência. Unidade: FOB
Subjects: DNA, ODONTOLOGIA LEGAL, SALIVA, BIOLOGIA MOLECULAR
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARVALHO, Suzana Papile Maciel et al. Avaliação da qualidade do DNA extraído de saliva humana armazenada e sua aplicabilidade na identificação em Odontologia Legal. Revista Odonto Ciência, v. 25, n. 1, p. 48-53, 2010Tradução . . Disponível em: http://revistaseletronicas.pucrs.br/ojs/index.php/fo/article/view/5043/4861. Acesso em: 23 maio 2024.
APA
Carvalho, S. P. M., Sales-Peres, A., Ribeiro-Bicudo, L. A., & Silva, R. H. A. da. (2010). Avaliação da qualidade do DNA extraído de saliva humana armazenada e sua aplicabilidade na identificação em Odontologia Legal. Revista Odonto Ciência, 25( 1), 48-53. Recuperado de http://revistaseletronicas.pucrs.br/ojs/index.php/fo/article/view/5043/4861
NLM
Carvalho SPM, Sales-Peres A, Ribeiro-Bicudo LA, Silva RHA da. Avaliação da qualidade do DNA extraído de saliva humana armazenada e sua aplicabilidade na identificação em Odontologia Legal [Internet]. Revista Odonto Ciência. 2010 ; 25( 1): 48-53.[citado 2024 maio 23 ] Available from: http://revistaseletronicas.pucrs.br/ojs/index.php/fo/article/view/5043/4861
Vancouver
Carvalho SPM, Sales-Peres A, Ribeiro-Bicudo LA, Silva RHA da. Avaliação da qualidade do DNA extraído de saliva humana armazenada e sua aplicabilidade na identificação em Odontologia Legal [Internet]. Revista Odonto Ciência. 2010 ; 25( 1): 48-53.[citado 2024 maio 23 ] Available from: http://revistaseletronicas.pucrs.br/ojs/index.php/fo/article/view/5043/4861
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
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: OFTALMOLOGIA, HOLOPROSENCEFALIA, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 maio 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 maio 23 ] 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 maio 23 ] Available from: https://repositorio.usp.br/directbitstream/2f0b2631-e279-402f-8a06-da3248e9768b/3099517.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
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: 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: 23 maio 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 maio 23 ] 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 maio 23 ] Available from: https://repositorio.usp.br/directbitstream/f3e2aad0-e9c8-482c-a8b6-4489251b91a8/3099540.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
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: FISSURA LÁBIOPALATINA, METABOLISMO, GENES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 maio 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 maio 23 ] 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 maio 23 ] 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
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: GENES, ANORMALIDADES CRANIOFACIAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 23 maio 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 maio 23 ] 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 maio 23 ] Available from: https://repositorio.usp.br/directbitstream/3070ceae-76f4-4f89-a6cc-a58f51202b63/3099790.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
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: 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: 23 maio 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 maio 23 ] 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 maio 23 ] Available from: https://repositorio.usp.br/directbitstream/0c0c52a0-6628-4cd2-8538-300b5e7b1447/3099502.pdf
Trabalho de evento-resumo
Holoprosencephaly-like: audiological and brainstem electrophysiological profiles (2009)
Antoneli, Melissa Zattoni; Ribeiro-Bicudo, Lucilene Arilho ; Zorzetto, N. L
Source: Anais. Conference titles: International Congress on Cleft Lip and Palate and Related Craniofacial Anomalies: Cleft and craniofacial care experience, evolution and innovation. Unidade: HRAC
Subjects: HOLOPROSENCEFALIA, AVALIAÇÃO AUDIOLÓGICA ELETROFISIOLÓGICA, TRONCO CEREBRAL
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANTONELI, Melissa Zattoni e RIBEIRO-BICUDO, Lucilene Arilho e ZORZETTO, N. L. Holoprosencephaly-like: audiological and brainstem electrophysiological profiles. 2009, Anais.. Fortaleza: SOBRAPAR, 2009. Disponível em: https://repositorio.usp.br/directbitstream/cadd3488-fc36-4383-8c5b-968776436717/3099532.pdf. Acesso em: 23 maio 2024.
APA
Antoneli, M. Z., Ribeiro-Bicudo, L. A., & Zorzetto, N. L. (2009). Holoprosencephaly-like: audiological and brainstem electrophysiological profiles. In Anais. Fortaleza: SOBRAPAR. Recuperado de https://repositorio.usp.br/directbitstream/cadd3488-fc36-4383-8c5b-968776436717/3099532.pdf
NLM
Antoneli MZ, Ribeiro-Bicudo LA, Zorzetto NL. Holoprosencephaly-like: audiological and brainstem electrophysiological profiles [Internet]. Anais. 2009 ;[citado 2024 maio 23 ] Available from: https://repositorio.usp.br/directbitstream/cadd3488-fc36-4383-8c5b-968776436717/3099532.pdf
Vancouver
Antoneli MZ, Ribeiro-Bicudo LA, Zorzetto NL. Holoprosencephaly-like: audiological and brainstem electrophysiological profiles [Internet]. Anais. 2009 ;[citado 2024 maio 23 ] Available from: https://repositorio.usp.br/directbitstream/cadd3488-fc36-4383-8c5b-968776436717/3099532.pdf

USP Schools

ReP

Filtros

Departament

Authors

USP affiliated authors

Date published

Subjects

Source title

Countries/Territories

Indexado em

Non normalized affiliation

Countries of institutions of collaboration