ReP USP - Resultado da busca

Artigo de periodico
Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients (2004)
Bassi, C. L.; Martelli, Lúcia Regina; Cipolotti, R.; Scrideli, C. A.; Defavery, R.; Tone, Luiz Gonzaga
Source: Brazilian Journal of Medical and Biological Research. Unidade: FMRP
Subjects: ONCOLOGIA, PEDIATRIA, GENÉTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BASSI, C. L. et al. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, v. 37, n. 11, p. 1683-1687, 2004Tradução . . Disponível em: https://doi.org/10.1590/s0100-879x2004001100014. Acesso em: 22 out. 2025.
APA
Bassi, C. L., Martelli, L. R., Cipolotti, R., Scrideli, C. A., Defavery, R., & Tone, L. G. (2004). Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients. Brazilian Journal of Medical and Biological Research, 37( 11), 1683-1687. doi:10.1590/s0100-879x2004001100014
NLM
Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2025 out. 22 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014
Vancouver
Bassi CL, Martelli LR, Cipolotti R, Scrideli CA, Defavery R, Tone LG. Lack of evidence for mutations or deletions in the CDKN2A/p16 and CDKN2B/p15 genes of Brazilian neuroblastoma patients [Internet]. Brazilian Journal of Medical and Biological Research. 2004 ; 37( 11): 1683-1687.[citado 2025 out. 22 ] Available from: https://doi.org/10.1590/s0100-879x2004001100014
Trabalho de evento-resumo periodico
B lineage acute lymphoid leukemia transformation in a child with JMML and type 1 neurofibromatosis with monosomy 7 (2002)
Baruffi, Marcelo Razera; Scrideli, Carlos Alberto; Valera, E.T.; Defavery, R.; Rogatto, S.; Tone, Luiz Gonzaga
Source: Medical & Pediatric Oncology. Conference titles: International Society of Pediatric Oncology Meeting. Unidade: FMRP
Subjects: PEDIATRIA, ONCOLOGIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARUFFI, Marcelo Razera et al. B lineage acute lymphoid leukemia transformation in a child with JMML and type 1 neurofibromatosis with monosomy 7. Medical & Pediatric Oncology. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 22 out. 2025. , 2002
APA
Baruffi, M. R., Scrideli, C. A., Valera, E. T., Defavery, R., Rogatto, S., & Tone, L. G. (2002). B lineage acute lymphoid leukemia transformation in a child with JMML and type 1 neurofibromatosis with monosomy 7. Medical & Pediatric Oncology. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Baruffi MR, Scrideli CA, Valera ET, Defavery R, Rogatto S, Tone LG. B lineage acute lymphoid leukemia transformation in a child with JMML and type 1 neurofibromatosis with monosomy 7. Medical & Pediatric Oncology. 2002 ; 39( 4): 324 res. P186.[citado 2025 out. 22 ]
Vancouver
Baruffi MR, Scrideli CA, Valera ET, Defavery R, Rogatto S, Tone LG. B lineage acute lymphoid leukemia transformation in a child with JMML and type 1 neurofibromatosis with monosomy 7. Medical & Pediatric Oncology. 2002 ; 39( 4): 324 res. P186.[citado 2025 out. 22 ]
Trabalho de evento-resumo periodico
Detection of RB-1 deletions in childhood acute myeloid leukemia by fish (2000)
Sankarankutty, B. M. O. M.; Bassi, C. L.; Scrideli, Carlos Alberto; Defavery, R.
Source: Medical and Pediatric Oncology. Conference titles: Meeting of the International Society of Paediatric Oncology. Unidade: FMRP
Subjects: PEDIATRIA, LEUCEMIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANKARANKUTTY, B. M. O. M. et al. Detection of RB-1 deletions in childhood acute myeloid leukemia by fish. Medical and Pediatric Oncology. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 22 out. 2025. , 2000
APA
Sankarankutty, B. M. O. M., Bassi, C. L., Scrideli, C. A., & Defavery, R. (2000). Detection of RB-1 deletions in childhood acute myeloid leukemia by fish. Medical and Pediatric Oncology. New York: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo.
NLM
Sankarankutty BMOM, Bassi CL, Scrideli CA, Defavery R. Detection of RB-1 deletions in childhood acute myeloid leukemia by fish. Medical and Pediatric Oncology. 2000 ; 34( 3):[citado 2025 out. 22 ]
Vancouver
Sankarankutty BMOM, Bassi CL, Scrideli CA, Defavery R. Detection of RB-1 deletions in childhood acute myeloid leukemia by fish. Medical and Pediatric Oncology. 2000 ; 34( 3):[citado 2025 out. 22 ]

USP Schools

ReP

Filtros

Authors

Indexado em