Filtros : "CASARTELLI, CACILDA" "Estados Unidos" Removido: "1998" Limpar

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  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS

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      ALMEIDA, Luciana Oliveira de et al. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, v. 198, n. 1, p. 15-21, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.11.013. Acesso em: 05 out. 2024.
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      Almeida, L. O. de, Custódio, A. C., Santos, M. J. dos, Almeida, J. R. W., Clara, C. A., Pinto, G. R., et al. (2010). The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival. Cancer Genetics and Cytogenetics, 198( 1), 15-21. doi:10.1016/j.cancergencyto.2009.11.013
    • NLM

      Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
    • Vancouver

      Almeida LO de, Custódio AC, Santos MJ dos, Almeida JRW, Clara CA, Pinto GR, Rey JA, Casartelli C. The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 198( 1): 15-21.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: MENINGIOMA, EXPRESSÃO GÊNICA

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      MARTÍNEZ-GLEZ, Victor et al. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, v. 196, n. 1, p. 1-6, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2009.08.003. Acesso em: 05 out. 2024.
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      Martínez-Glez, V., Alvarez, L., Franco-Hernández, C., Torres-Martin, M., Campos, J. M. de, Isla, A., et al. (2010). Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas. Cancer Genetics and Cytogenetics, 196( 1), 1-6. doi:10.1016/j.cancergencyto.2009.08.003
    • NLM

      Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
    • Vancouver

      Martínez-Glez V, Alvarez L, Franco-Hernández C, Torres-Martin M, Campos JM de, Isla A, Vaquero J, Lassaletta L, Castresana JS, Casartelli C, Rey JA. Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas [Internet]. Cancer Genetics and Cytogenetics. 2010 ; 196( 1): 1-6.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: NEOPLASIAS, GENÉTICA

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      FRANCO-HERNÁNDEZ, Carmen et al. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, v. 190, n. 2, p. 93-96, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2008.09.017. Acesso em: 05 out. 2024.
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      Franco-Hernández, C., Martínez-Glez, V., Campos, J. M. de, Isla, A., Vaquero, J., Gutiérrez, M., et al. (2009). Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. Cancer Genetics and Cytogenetics, 190( 2), 93-96. doi:10.1016/j.cancergencyto.2008.09.017
    • NLM

      Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
    • Vancouver

      Franco-Hernández C, Martínez-Glez V, Campos JM de, Isla A, Vaquero J, Gutiérrez M, Casartelli C, Rey JA. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity [Internet]. Cancer Genetics and Cytogenetics. 2009 ; 190( 2): 93-96.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
  • Source: Journal of Neuro-Oncology. Unidade: FMRP

    Subjects: MUTAÇÃO GENÉTICA, PROGNÓSTICO, GENÉTICA MÉDICA

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      PINTO, Giovanny Rebouças et al. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, v. 90, n. 3, p. 253-258, 2008Tradução . . Disponível em: https://doi.org/10.1007/s11060-008-9664-8. Acesso em: 05 out. 2024.
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      Pinto, G. R., Yoshioka, F. K. N., Clara, C. A., Santos, M. J. dos, Almeida, J. R. W. de, Burbano, R. R., et al. (2008). WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil. Journal of Neuro-Oncology, 90( 3), 253-258. doi:10.1007/s11060-008-9664-8
    • NLM

      Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 out. 05 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
    • Vancouver

      Pinto GR, Yoshioka FKN, Clara CA, Santos MJ dos, Almeida JRW de, Burbano RR, Rey JA, Casartelli C. WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil [Internet]. Journal of Neuro-Oncology. 2008 ; 90( 3): 253-258.[citado 2024 out. 05 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: POLIMORFISMO, NEOPLASIAS

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      TORRES-MARTÍN, et al. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 out. 2024. , 2008
    • APA

      Torres-Martín,, Franco-Hernandez, C., Matinez-Glez, V., Campos, J. M. de, Isla, A., Casartelli, C., & Rey, J. A. (2008). Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2024 out. 05 ]
    • Vancouver

      Torres-Martín, Franco-Hernandez C, Matinez-Glez V, Campos JM de, Isla A, Casartelli C, Rey JA. Mutation analysis of the CITED4 gene in glioblastomas. [Carta]. Cancer Genetics and Cytogenetics. 2008 ; 185( 2): 114-116.[citado 2024 out. 05 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: NEOPLASIAS MAMÁRIAS, MUTAÇÃO GENÉTICA

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      LACERDA, Leandra Linhares et al. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, v. 160, p. 160-163, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.cancergencyto.2004.11.014. Acesso em: 05 out. 2024.
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      Lacerda, L. L., Serrano, S. V., Mathes, Â. do C. da S., Rey, J. A., Bello, M. J., & Casartelli, C. (2005). An intronic variant in the TP53 gene in a Brazilian woman with breast cancer. Cancer Genetics and Cytogenetics, 160, 160-163. doi:10.1016/j.cancergencyto.2004.11.014
    • NLM

      Lacerda LL, Serrano SV, Mathes  do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
    • Vancouver

      Lacerda LL, Serrano SV, Mathes  do C da S, Rey JA, Bello MJ, Casartelli C. An intronic variant in the TP53 gene in a Brazilian woman with breast cancer [Internet]. Cancer Genetics and Cytogenetics. 2005 ; 160 160-163.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
  • Source: Câncer Therapy. Unidade: FMRP

    Assunto: GASTROENTEROPATIAS (GENÉTICA)

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      BELLO, M. Josefa et al. Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy, v. 2, p. 187-194, 2004Tradução . . Acesso em: 05 out. 2024.
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      Bello, M. J., Gonzales-Gomez, P., Alonso, M. E., Anselmo, N. P., Arjona, D., Amiñoso, C., et al. (2004). Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy, 2, 187-194.
    • NLM

      Bello MJ, Gonzales-Gomez P, Alonso ME, Anselmo NP, Arjona D, Amiñoso C, Lopez-Marin I, Campos JM, Isla A, Vaquero J, Casartelli C, Rey JA. Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy. 2004 ; 2 187-194.[citado 2024 out. 05 ]
    • Vancouver

      Bello MJ, Gonzales-Gomez P, Alonso ME, Anselmo NP, Arjona D, Amiñoso C, Lopez-Marin I, Campos JM, Isla A, Vaquero J, Casartelli C, Rey JA. Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas. Câncer Therapy. 2004 ; 2 187-194.[citado 2024 out. 05 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Assunto: MENINGIOMA

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      LOMAS, Jesus et al. Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, v. 129, p. 88-91, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00430-7. Acesso em: 05 out. 2024.
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      Lomas, J., Bello, J., Arjona, D., Gonzales-Gomez, P., Alonso, M. E., Campos, J. M. de, et al. (2001). Analysis of p73 gene in meningiomas with deletion at 1p. Cancer Genetics and Cytogenetics, 129, 88-91. doi:10.1016/s0165-4608(01)00430-7
    • NLM

      Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
    • Vancouver

      Lomas J, Bello J, Arjona D, Gonzales-Gomez P, Alonso ME, Campos JM de, Vaquero J, Ruiz-Barnes P, Sarasa JL, Casartelli C, Rey JA. Analysis of p73 gene in meningiomas with deletion at 1p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 88-91.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: LINFOMA, TESTÍCULO, GENÉTICA MÉDICA

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      ESPINOZA, Luis A. et al. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, v. 131, p. 79-81, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00495-2. Acesso em: 05 out. 2024.
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      Espinoza, L. A., Barbieri Neto, J., Popescu, N. C., & Casartelli, C. (2001). Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma. Cancer Genetics and Cytogenetics, 131, 79-81. doi:10.1016/s0165-4608(01)00495-2
    • NLM

      Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
    • Vancouver

      Espinoza LA, Barbieri Neto J, Popescu NC, Casartelli C. Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 131 79-81.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: CISTOS, OSSO E OSSOS, CITOGENÉTICA

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      BARUFFI, Marcelo Razera et al. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, v. 129, p. 177-180, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(01)00453-8. Acesso em: 05 out. 2024.
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      Baruffi, M. R., Barbieri Neto, J., Barbieri, C. H., & Casartelli, C. (2001). Aneurysmal bone cyst with chromosomal changes involving 7q and 16p. Cancer Genetics and Cytogenetics, 129, 177-180. doi:10.1016/s0165-4608(01)00453-8
    • NLM

      Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
    • Vancouver

      Baruffi MR, Barbieri Neto J, Barbieri CH, Casartelli C. Aneurysmal bone cyst with chromosomal changes involving 7q and 16p [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 129 177-180.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: ONCOLOGIA, OSSO E OSSOS (CIRURGIA), CITOGENÉTICA

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      BARUFFI, Marcelo Razera et al. Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, v. 124, p. 127-131, 2001Tradução . . Disponível em: https://doi.org/10.1016/s0165-4608(00)00327-7. Acesso em: 05 out. 2024.
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      Baruffi, M. R., Volpon, J. B., Barbieri Neto, J., & Casartelli, C. (2001). Osteoid osteomas with chromosome alterations involving 22q. Cancer Genetics and Cytogenetics, 124, 127-131. doi:10.1016/s0165-4608(00)00327-7
    • NLM

      Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
    • Vancouver

      Baruffi MR, Volpon JB, Barbieri Neto J, Casartelli C. Osteoid osteomas with chromosome alterations involving 22q [Internet]. Cancer Genetics and Cytogenetics. 2001 ; 124 127-131.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
  • Source: Cancer Genetics Cytogenetics. Unidade: FMRP

    Subjects: GENÉTICA MÉDICA, ONCOLOGIA, NEOPLASIAS, MAMA, DOENÇAS DOS GENITAIS FEMININOS

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      BURBANO, Rommel Rodríguez et al. Trisomy 4 in a case of gynecomastia. Cancer Genetics Cytogenetics, v. 117, p. 143-145, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf. Acesso em: 05 out. 2024.
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      Burbano, R. R., Barbieri Neto, J., Philbert, P. M. de P., Lemos, J. A., Bahia, M., & Casartelli, C. (2000). Trisomy 4 in a case of gynecomastia. Cancer Genetics Cytogenetics, 117, 143-145. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
    • NLM

      Burbano RR, Barbieri Neto J, Philbert PM de P, Lemos JA, Bahia M, Casartelli C. Trisomy 4 in a case of gynecomastia [Internet]. Cancer Genetics Cytogenetics. 2000 ; 117 143-145.[citado 2024 out. 05 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
    • Vancouver

      Burbano RR, Barbieri Neto J, Philbert PM de P, Lemos JA, Bahia M, Casartelli C. Trisomy 4 in a case of gynecomastia [Internet]. Cancer Genetics Cytogenetics. 2000 ; 117 143-145.[citado 2024 out. 05 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
  • Source: Cancer Genetics Cytogenetics. Unidade: FMRP

    Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA

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      BURBANO, Rommel Rodríguez et al. Cytogenetics of epithelial hyperplasias of the human breast. Cancer Genetics Cytogenetics, v. 119, p. 62-66, 2000Tradução . . Disponível em: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf. Acesso em: 05 out. 2024.
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      Burbano, R. R., Medeiros, A., Amorim, M. I. M. de, Lima, E. M., Mello, A., Barbieri Neto, J., & Casartelli, C. (2000). Cytogenetics of epithelial hyperplasias of the human breast. Cancer Genetics Cytogenetics, 119, 62-66. Recuperado de http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
    • NLM

      Burbano RR, Medeiros A, Amorim MIM de, Lima EM, Mello A, Barbieri Neto J, Casartelli C. Cytogenetics of epithelial hyperplasias of the human breast [Internet]. Cancer Genetics Cytogenetics. 2000 ; 119 62-66.[citado 2024 out. 05 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
    • Vancouver

      Burbano RR, Medeiros A, Amorim MIM de, Lima EM, Mello A, Barbieri Neto J, Casartelli C. Cytogenetics of epithelial hyperplasias of the human breast [Internet]. Cancer Genetics Cytogenetics. 2000 ; 119 62-66.[citado 2024 out. 05 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
  • Source: Gynecologic Oncology. Unidade: FMRP

    Subjects: NEOPLASIAS, ONCOLOGIA, GINECOLOGIA

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      MANTOVANI, M. S. et al. Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology, v. 72, p. 71-75, 1999Tradução . . Acesso em: 05 out. 2024.
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      Mantovani, M. S., Barbieri Neto, J., Philbert, P. M. de P., & Casartelli, C. (1999). Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology, 72, 71-75.
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      Mantovani MS, Barbieri Neto J, Philbert PM de P, Casartelli C. Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology. 1999 ; 72 71-75.[citado 2024 out. 05 ]
    • Vancouver

      Mantovani MS, Barbieri Neto J, Philbert PM de P, Casartelli C. Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology. 1999 ; 72 71-75.[citado 2024 out. 05 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Subjects: ONCOLOGIA, GENÉTICA MÉDICA, GASTROENTEROLOGIA

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      ESPINOZA, Luis A e BARBIERI NETO, José e CASARTELLI, Cacilda. Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics, v. 109, n. 1, p. 45-50, 1999Tradução . . Acesso em: 05 out. 2024.
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      Espinoza, L. A., Barbieri Neto, J., & Casartelli, C. (1999). Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics, 109( 1), 45-50.
    • NLM

      Espinoza LA, Barbieri Neto J, Casartelli C. Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics. 1999 ; 109( 1): 45-50.[citado 2024 out. 05 ]
    • Vancouver

      Espinoza LA, Barbieri Neto J, Casartelli C. Pathological and karyotypic abnormalities in advanced gastric carcinomas. Cancer Genetics and Cytogenetics. 1999 ; 109( 1): 45-50.[citado 2024 out. 05 ]
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Assunto: GENÉTICA

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      ROGATTO, S R et al. Chromosomes in the genesis and progression of ependynomas. Cancer Genetics and Cytogenetics, v. 69, p. 146-52, 1993Tradução . . Disponível em: https://doi.org/10.1016/0165-4608(93)90093-2. Acesso em: 05 out. 2024.
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      Rogatto, S. R., Casartelli, C., Rainho, C. A., & Barbieri Neto, J. (1993). Chromosomes in the genesis and progression of ependynomas. Cancer Genetics and Cytogenetics, 69, 146-52. doi:10.1016/0165-4608(93)90093-2
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      Rogatto SR, Casartelli C, Rainho CA, Barbieri Neto J. Chromosomes in the genesis and progression of ependynomas [Internet]. Cancer Genetics and Cytogenetics. 1993 ;69 146-52.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/0165-4608(93)90093-2
    • Vancouver

      Rogatto SR, Casartelli C, Rainho CA, Barbieri Neto J. Chromosomes in the genesis and progression of ependynomas [Internet]. Cancer Genetics and Cytogenetics. 1993 ;69 146-52.[citado 2024 out. 05 ] Available from: https://doi.org/10.1016/0165-4608(93)90093-2
  • Source: Cancer Genetics and Cytogenetics. Unidade: FMRP

    Assunto: GENÉTICA MÉDICA

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    • ABNT

      CASARTELLI, C et al. Benign pathologies: cytogenetic analysis. Cancer Genetics and Cytogenetics, v. 63, n. 2 , p. 157, 1992Tradução . . Acesso em: 05 out. 2024.
    • APA

      Casartelli, C., Rodriguez Burbano, R., Barbieri Neto, J., Philbert, P. M. P., & Mathes, A. C. S. (1992). Benign pathologies: cytogenetic analysis. Cancer Genetics and Cytogenetics, 63( 2 ), 157.
    • NLM

      Casartelli C, Rodriguez Burbano R, Barbieri Neto J, Philbert PMP, Mathes ACS. Benign pathologies: cytogenetic analysis. Cancer Genetics and Cytogenetics. 1992 ;63( 2 ): 157.[citado 2024 out. 05 ]
    • Vancouver

      Casartelli C, Rodriguez Burbano R, Barbieri Neto J, Philbert PMP, Mathes ACS. Benign pathologies: cytogenetic analysis. Cancer Genetics and Cytogenetics. 1992 ;63( 2 ): 157.[citado 2024 out. 05 ]
  • Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: FMRP

    Assunto: GENÉTICA

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      CASARTELLI, C et al. Benign mammary pathologies cytogenetic findings. American Journal of Human Genetics. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 out. 2024. , 1991
    • APA

      Casartelli, C., Costa, M. I. A., Rogatto, S. R., Philbert, P. M. P., Barbieri Neto, J., & Mathes, A. C. S. (1991). Benign mammary pathologies cytogenetic findings. American Journal of Human Genetics. Washington: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Casartelli C, Costa MIA, Rogatto SR, Philbert PMP, Barbieri Neto J, Mathes ACS. Benign mammary pathologies cytogenetic findings. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 239.[citado 2024 out. 05 ]
    • Vancouver

      Casartelli C, Costa MIA, Rogatto SR, Philbert PMP, Barbieri Neto J, Mathes ACS. Benign mammary pathologies cytogenetic findings. American Journal of Human Genetics. 1991 ;49( 4 suppl.): 239.[citado 2024 out. 05 ]
  • Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: FMRP

    Subjects: GENÉTICA, GENÉTICA

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ROGATTO, S R e CASARTELLI, C e BARBIERI NETO, J. Chromosomal abnormalities in ependynomas and medulloblastomas. American Journal of Human Genetics. [S.l.]: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 out. 2024. , 1991
    • APA

      Rogatto, S. R., Casartelli, C., & Barbieri Neto, J. (1991). Chromosomal abnormalities in ependynomas and medulloblastomas. American Journal of Human Genetics. Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Rogatto SR, Casartelli C, Barbieri Neto J. Chromosomal abnormalities in ependynomas and medulloblastomas. American Journal of Human Genetics. 1991 ;49( 4 ): 248.[citado 2024 out. 05 ]
    • Vancouver

      Rogatto SR, Casartelli C, Barbieri Neto J. Chromosomal abnormalities in ependynomas and medulloblastomas. American Journal of Human Genetics. 1991 ;49( 4 ): 248.[citado 2024 out. 05 ]
  • Source: Abstracts. Conference titles: International Workshop on Chromossomes in Solid Tumors. Unidade: FMRP

    Assunto: GENÉTICA

    How to cite
    A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
    • ABNT

      ROGATTO, S R e CASARTELLI, C e BARBIERI NETO, J. Cytogenetic study of human gliomas. 1989, Anais.. Arizona: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 1989. . Acesso em: 05 out. 2024.
    • APA

      Rogatto, S. R., Casartelli, C., & Barbieri Neto, J. (1989). Cytogenetic study of human gliomas. In Abstracts. Arizona: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
    • NLM

      Rogatto SR, Casartelli C, Barbieri Neto J. Cytogenetic study of human gliomas. Abstracts. 1989 ;[citado 2024 out. 05 ]
    • Vancouver

      Rogatto SR, Casartelli C, Barbieri Neto J. Cytogenetic study of human gliomas. Abstracts. 1989 ;[citado 2024 out. 05 ]

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