Mutations in the fanconi anemia Group C gene in the State of São Paulo-Brazil (1999)
- Authors:
- Autor USP: TONE, LUIZ GONZAGA - FMRP
- Unidade: FMRP
- Assunto: HEMATOLOGIA
- Language: Inglês
- Imprenta:
- Publisher place: Foz do Iguaçu
- Date published: 1999
- Conference titles: Congresso Nacional do Colégio Brasileiro de Hematologia
-
ABNT
RODRIGUEZ, D. et al. Mutations in the fanconi anemia Group C gene in the State of São Paulo-Brazil. 1999, Anais.. Foz do Iguaçu: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo, 1999. . Acesso em: 13 fev. 2026. -
APA
Rodriguez, D., Lima, C. S. P., Figueiredo, M. S., Carneiro, J. D. A., Tone, L. G., & Bertuzzu, C. S. (1999). Mutations in the fanconi anemia Group C gene in the State of São Paulo-Brazil. In . Foz do Iguaçu: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Rodriguez D, Lima CSP, Figueiredo MS, Carneiro JDA, Tone LG, Bertuzzu CS. Mutations in the fanconi anemia Group C gene in the State of São Paulo-Brazil. 1999 ;[citado 2026 fev. 13 ] -
Vancouver
Rodriguez D, Lima CSP, Figueiredo MS, Carneiro JDA, Tone LG, Bertuzzu CS. Mutations in the fanconi anemia Group C gene in the State of São Paulo-Brazil. 1999 ;[citado 2026 fev. 13 ] - Linfoma nao hodgkin de grandes celulas anaplasicas 'CD30 POT.+' - Estudo de 1 caso
- Development of a culturally appropriate portuguese version of the Gap-Kalamazoo communication skills assessment form (GKCSAF) for the evaluation of interpersonal and communication competences in Brazilian Medical Education
- New recurrent deletions in the PPAR"gama" and TP53 genes are associated with childhood myelodysplastic syndrome
- Childhood leukemia
- Avaliacao do estado nutricional de criancas portadoras de neoplasia maligna
- Tratamento clínico do linfangioma com alfa-2a-interferon
- Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients
- Grupos para acompanhantes de crianças e adolescentes com câncer em uma casa de apoio
- B lineage acute lymphoblastic leukemia transformation in child with juvenile myelomonocytic leumemia, type 1 neurofibromatosis and monosomy of chromosome 7 possible implications in the leukemogenesis
- T cell receptor gamma (TCRG) gene rearrangements in Brazilian children with acute lymphoblastic leukemia: analysis and implications for the study of minimal residual disease
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas