área de pesquisa
- Expanding the phenotype of 8p23.1 deletion syndrome: Eight new cases resembling the clinical spectrum of 22q11.2 microdeletion
- Increased sMer, but not sAxl, sTyro3, and Gas6 relate with active disease in juvenile systemic lupus erythematosus
- Investigação genético-molecular de pacientes com Imunodeficiência Combinada Grave
- Lucila Akune Barreiros
- Luiz Euribel Prestes Carneiro
- PATRICIA PALMEIRA