Sökresultat - Carlos Fernández-Lago

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)?) av Celeste Bento, Helena Almeida, Tabita Maia, Luís Relvas, Ana Catarina Oliveira, Cédric Rossi, François Girodon, Carlos Fernández-Lago, Ascension Aguado‐Diaz, Cristina Fraga, Ricardo Marques da Costa, Ana Luiza Rosa de Araújo, João S. Silva, Helena Vitória, Natalina Miguel, Maria Pedro Silveira, Guillermo Martín–Núñez, Letícia Ribeiro