erythrocytosis

n.

红细胞增多（症）；

PHD2 mutation and congenital erythrocytosis with paraganglioma.
A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis
JAK2 exon 12 mutations in polycythemia vera or idiopathic erythrocytosis
A Gain-of-Function Mutation in the HIF2A Gene in Familial Erythrocytosis
JAK2 Exon 12 Mutations in Polycythemia Vera and Idiopathic Erythrocytosis
Stratton A: Jak2 exon12 mutation in polycythemia vera and idiopathic erythrocytosis
Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosis.
Guidelines for the diagnosis, investigation and management of polycythaemia/erythrocytosis
Capecitabine and Oxaliplatin for Advanced Esophagogastric Cancer The HIF2A Gene in Familial Erythrocytosis
Percy, M. J. et al. A family with erythrocytosis establishes a role for prolyl hydroxylase domain protein 2 in oxygen homeostasis. P...