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Issue Date | Title | Author(s) |
---|---|---|
2018 | High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype | DEZAN, Marcia Regina; OLIVEIRA, Valeria B.; GOMES, Carolina Nunes; LUZ, Fabio; GALLUCCI, Antonio J.; BONIFACIO, Silvia L.; ALENCAR, Cecilia Salete; SABINO, Ester C.; PEREIRA, Alexandre C.; KRIEGER, Jose E.; ROCHA, Vanderson; MENDRONE-JUNIOR, Alfredo; DINARDO, Carla L. |
2017 | RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients | DEZAN, Marcia R.; RIBEIRO, Ingrid Helena; OLIVEIRA, Valeria B.; VIEIRA, Juliana B.; GOMES, Francisco C.; FRANCO, Lucas A. M.; VARUZZA, Leonardo; RIBEIRO, Roberto; CHINOCA, Karen Ziza; LEVI, Jose Eduardo; KRIEGER, Jose Eduardo; PEREIRA, Alexandre Costa; GUALANDRO, Sandra F. M.; ROCHA, Vanderson G.; MENDRONE-JUNIOR, Alfredo; SABINO, Ester Cerdeira; DINARDO, Carla Luana |
2020 | Effectiveness of strategies to screen for blood donors with RH variants in a mixed population | ALMEIDA, Fabio Augusto Abreu de; DEZAN, Marcia Regina; OLIVEIRA, Valeria Brito; ALENCAR, Cecilia Salete; LUZ, Fabio; KRIEGER, Jose Eduardo; PEREIRA, Alexandre Costa; SABINO, Ester Cerdeira; ROCHA, Vanderson; MENDRONE-JUNIOR, Alfredo; DINARDO, Carla Luana |
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