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Artigo de periodico
The A61 G EGF polymorphism is associated with development of extraaxial nervous system tumors but not with overall survival (2010)
Almeida, Luciana Oliveira de; Custódio, Aline Cadurin; Santos, Marcelo José dos; Almeida, José R. W.; Clara, Carlos Afonso; Pinto, Giovanny Rebouças; Rey, Juan A.; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS CEREBRAIS
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.11.013
Artigo de periodico
Genomic deletions at 1p and 14p are associated with an abnormal cDNA microarray gene expression pattern in meningiomas but not it schwannomas (2010)
Martínez-Glez, Victor; Alvarez, Luis; Franco-Hernández, Carmen; Torres-Martin, Miguel; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Lassaletta, Luis; Castresana, Javier S.; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: MENINGIOMA, EXPRESSÃO GÊNICA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/j.cancergencyto.2009.08.003
Artigo de periodico
Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity (2009)
Franco-Hernández, Carmen; Martínez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Vaquero, Jesús; Gutiérrez, Manuel; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: NEOPLASIAS, GENÉTICA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/j.cancergencyto.2008.09.017
Artigo de periodico
WRN Cys1367Arg SNP is not associated with risk and prognosis of gliomas in Southeast Brasil (2008)
Pinto, Giovanny Rebouças; Yoshioka, France Keiko Nascimento; Clara, Carlos Afonso; Santos, Marcelo José dos; Almeida, José Reynaldo Walther de; Burbano, Rommel Rodríguez; Rey, Juan A.; Casartelli, Cacilda
Source: Journal of Neuro-Oncology. Unidade: FMRP
Subjects: MUTAÇÃO GENÉTICA, PROGNÓSTICO, GENÉTICA MÉDICA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1007/s11060-008-9664-8
Artigo de periodico-carta/editorial
Mutation analysis of the CITED4 gene in glioblastomas. [Carta] (2008)
Torres-Martín; Franco-Hernandez, Carmen; Matinez-Glez, Victor; Campos, Jose M. de; Isla, Alberto; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: POLIMORFISMO, NEOPLASIAS
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ABNT
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: 08 nov. 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 nov. 08 ]
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 nov. 08 ]
Artigo de periodico
An intronic variant in the TP53 gene in a Brazilian woman with breast cancer (2005)
Lacerda, Leandra Linhares; Serrano, Sérgio Vicente; Mathes, Ângelo do Carmo da Silva; Rey, Juan A.; Bello, Maria Josefa; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: NEOPLASIAS MAMÁRIAS, MUTAÇÃO GENÉTICA
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ABNT
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: 08 nov. 2024.
APA
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 Â 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 nov. 08 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
Vancouver
Lacerda LL, Serrano SV, Mathes Â 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 nov. 08 ] Available from: https://doi.org/10.1016/j.cancergencyto.2004.11.014
Artigo de periodico
Methylation analysis of cell cycle control genes RB1, 'p14 IND ARF' and 'p16 IND INK4a' in human gliomas (2004)
Bello, M. Josefa; Gonzales-Gomez, Pilar; Alonso, M. Eva; Anselmo, Nilson P.; Arjona, Dolores; Amiñoso, Cinthia; Lopez-Marin, Isabel; Campos, José M.; Isla, Alberto; Vaquero, Jesus; Casartelli, Cacilda; Rey, Juan A.
Source: Câncer Therapy. Unidade: FMRP
Assunto: GASTROENTEROPATIAS (GENÉTICA)
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ]
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 nov. 08 ]
Artigo de periodico
Analysis of p73 gene in meningiomas with deletion at 1p (2001)
Lomas, Jesus; Bello, Josefa; Arjona, Dolores; Gonzales-Gomez, Pilar; Alonso, M. Eva; Campos, José M. de; Vaquero, Jesus; Ruiz-Barnes, Pedro; Sarasa, José L.; Casartelli, Cacilda; Rey, Juan A.
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assunto: MENINGIOMA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/s0165-4608(01)00430-7
Artigo de periodico
Deletion 5p11 accompanied by multiple numerical changes in testicular lymphoma (2001)
Espinoza, Luis A.; Barbieri Neto, José; Popescu, Nicholas C.; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: LINFOMA, TESTÍCULO, GENÉTICA MÉDICA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/s0165-4608(01)00495-2
Artigo de periodico
Aneurysmal bone cyst with chromosomal changes involving 7q and 16p (2001)
Baruffi, Marcelo Razera; Barbieri Neto, José; Barbieri, Claudio Henrique; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: CISTOS, OSSO E OSSOS, CITOGENÉTICA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/s0165-4608(01)00453-8
Artigo de periodico
Osteoid osteomas with chromosome alterations involving 22q (2001)
Baruffi, Marcelo Razera; Volpon, José Batista; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: ONCOLOGIA, OSSO E OSSOS (CIRURGIA), CITOGENÉTICA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/s0165-4608(00)00327-7
Artigo de periodico
Trisomy 4 in a case of gynecomastia (2000)
Burbano, Rommel Rodríguez; Barbieri Neto, José; Philbert, Paulo Meyer de Paula; Lemos, José Alexandre; Bahia, Marcelo; Casartelli, Cacilda
Source: Cancer Genetics Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, NEOPLASIAS, MAMA, DOENÇAS DOS GENITAIS FEMININOS
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v117i0002&article=143_t4iacog&form=pdf&file=file.pdf
Artigo de periodico
Cytogenetics of epithelial hyperplasias of the human breast (2000)
Burbano, Rommel Rodríguez; Medeiros, Arnaldo; Amorim, Marucia Irena Medeiros de; Lima, Eleonidas Moura; Mello, Adriano; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, ONCOLOGIA, MAMA
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ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ] 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 nov. 08 ] Available from: http://probe.usp.br/cgi-bin/sciserv.pl?collection=journals&journal=01654608&issue=v119i0001&article=62_coehothb&form=pdf&file=file.pdf
Artigo de periodico
Multiple uterine leiomyomas: Cytogenetic analysis (1999)
Mantovani, M. S.; Barbieri Neto, José; Philbert, Paulo Meyer de Paula; Casartelli, Cacilda
Source: Gynecologic Oncology. Unidade: FMRP
Subjects: NEOPLASIAS, ONCOLOGIA, GINECOLOGIA
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ABNT
MANTOVANI, M. S. et al. Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology, v. 72, p. 71-75, 1999Tradução . . Acesso em: 08 nov. 2024.
APA
Mantovani, M. S., Barbieri Neto, J., Philbert, P. M. de P., & Casartelli, C. (1999). Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology, 72, 71-75.
NLM
Mantovani MS, Barbieri Neto J, Philbert PM de P, Casartelli C. Multiple uterine leiomyomas: Cytogenetic analysis. Gynecologic Oncology. 1999 ; 72 71-75.[citado 2024 nov. 08 ]
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 nov. 08 ]
Artigo de periodico
Pathological and karyotypic abnormalities in advanced gastric carcinomas (1999)
Espinoza, Luis A; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: ONCOLOGIA, GENÉTICA MÉDICA, GASTROENTEROLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 08 nov. 2024.
APA
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 nov. 08 ]
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 nov. 08 ]
Artigo de periodico
Primary intracranial germ cell tumors without an isochromosome 12p (1998)
Lemos, Jose Alexandre Rodrigues de; Barbieri Neto, José; Casartelli, Cacilda
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Subjects: GENÉTICA MÉDICA, NEOPLASIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LEMOS, Jose Alexandre Rodrigues de e BARBIERI NETO, José e CASARTELLI, Cacilda. Primary intracranial germ cell tumors without an isochromosome 12p. Cancer Genetics and Cytogenetics, v. 100, p. 124-128, 1998Tradução . . Acesso em: 08 nov. 2024.
APA
Lemos, J. A. R. de, Barbieri Neto, J., & Casartelli, C. (1998). Primary intracranial germ cell tumors without an isochromosome 12p. Cancer Genetics and Cytogenetics, 100, 124-128.
NLM
Lemos JAR de, Barbieri Neto J, Casartelli C. Primary intracranial germ cell tumors without an isochromosome 12p. Cancer Genetics and Cytogenetics. 1998 ; 100 124-128.[citado 2024 nov. 08 ]
Vancouver
Lemos JAR de, Barbieri Neto J, Casartelli C. Primary intracranial germ cell tumors without an isochromosome 12p. Cancer Genetics and Cytogenetics. 1998 ; 100 124-128.[citado 2024 nov. 08 ]
Artigo de periodico
Chromosomes in the genesis and progression of ependynomas (1993)
Rogatto, S R; Casartelli, C; Rainho, C A; Barbieri Neto, J
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assunto: GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
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: 08 nov. 2024.
APA
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
NLM
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 nov. 08 ] 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 nov. 08 ] Available from: https://doi.org/10.1016/0165-4608(93)90093-2
Artigo de periodico
Benign pathologies: cytogenetic analysis (1992)
Casartelli, C; Rodriguez Burbano, R; Barbieri Neto, J; Philbert, P M P; Mathes, A C S
Source: Cancer Genetics and Cytogenetics. Unidade: FMRP
Assunto: GENÉTICA MÉDICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CASARTELLI, C et al. Benign pathologies: cytogenetic analysis. Cancer Genetics and Cytogenetics, v. 63, n. 2 , p. 157, 1992Tradução . . Acesso em: 08 nov. 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 nov. 08 ]
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 nov. 08 ]
Trabalho de evento-resumo periodico
Benign mammary pathologies cytogenetic findings (1991)
Casartelli, C; Costa, M I A; Rogatto, S R; Philbert, P M P; Barbieri Neto, J; Mathes, A C S
Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: FMRP
Assunto: GENÉTICA
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: 08 nov. 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 nov. 08 ]
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 nov. 08 ]
Trabalho de evento-resumo periodico
Chromosomal abnormalities in ependynomas and medulloblastomas (1991)
Rogatto, S R; Casartelli, C; Barbieri Neto, J
Source: American Journal of Human Genetics. Conference titles: International Congress of Human Genetics. Unidade: FMRP
Subjects: GENÉTICA, GENÉTICA
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: 08 nov. 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 nov. 08 ]
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 nov. 08 ]

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