H. Vitória

Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)

F. Girodon, C. Bento, C. Rossi, 2013, European journal of haematology.

Expression of CD44 and CD35 during normal and myelodysplastic erythropoiesis.

A. Órfão, P. Laranjeira, A. Paiva, 2015, Leukemia research.

CD43 and CD49d from the B‐Cell Chronic Lymphoproliferative Disorders Diagnostic Panel Are Useful to Detect Erythroid Dysplasia

A. Sarmento-Ribeiro, P. Laranjeira, A. Paiva, 2019, Cytometry. Part B, Clinical cytometry.

Preneoplastic somatic mutations including MYD88L265P in lymphoplasmacytic lymphoma

J. Martinez-Climent, F. Prósper, N. Puig, 2022, Science advances.

Genetic Basis of Congenital Erythrocytosis: Mutation Update and Online Databases

J. Palmblad, S. Rives, S. Richard, 2014, Human mutation.

Multiple myeloma in elderly patients—a Portuguese multicentric real-life study

H. Coelho, A. Jorge, T. Mendonça, 2019, Annals of Hematology.

Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)

F. Girodon, C. Bento, C. Rossi, 2013, European journal of haematology.