skip to main content
Idioma:
Refinado por: Base de dados/Biblioteca: BACON - Mir@bel - GLOBAL_LIBRESACCES remover tipo de recurso: Reports remover BioMedCentral remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
Material Type:
Report 		Adicionar ao Meu Espaço

An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia

Lovatel, Viviane Lamim ; de Souza, Daiane Corrêa ; Alvarenga, Tatiana Fonseca ; Capela de Matos, Roberto R ; Diniz, Claudia ; Schramm, Marcia Trindade ; Llerena Júnior, Juan Clinton ; Silva, Maria Luiza Macedo ; Abdelhay, Eliana ; de Souza Fernandez, Teresa

Molecular cytogenetics, 2018, Vol.11, p.40-40

Texto completo disponível

Citações Citado por
2
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome
A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome
Material Type:
Report 		Adicionar ao Meu Espaço

A unique set of complex chromosomal abnormalities in an infant with myeloid leukemia associated with Down syndrome

de Souza, Daiane Correa ; de Figueiredo, Amanda Faria ; Ney Garcia, Daniela R ; da Costa, Elaine Sobral ; Othman, Moneeb A K ; Liehr, Thomas ; Abdelhay, Eliana ; Silva, Maria Luiza Macedo ; de Souza Fernandez, Teresa

Molecular cytogenetics, 2017, Vol.10, p.35-35

Texto completo disponível

Citações Citado por
3
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia
Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia
Material Type:
Report 		Adicionar ao Meu Espaço

Molecular cytogenetic studies characterizing a novel complex karyotype with an uncommon 5q22 deletion in childhood acute myeloid leukemia

de Figueiredo, Amanda Faria ; Capela de Matos, Roberto Rodrigues ; Othman, Moneeb A K ; Liehr, Thomas ; da Costa, Elaine Sobral ; Land, Marcelo Geradin Poirot ; Ribeiro, Raul C ; Abdelhay, Eliana ; Silva, Maria Luiza Macedo

Molecular cytogenetics, 2015, Vol.8, p.62-62

Texto completo disponível

Citações Citado por

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Refinar Meus Resultados

Data de Publicação 

De até
Refinar

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.