hereditary spherocytosis
[hiˈreditəri ˈsfiərəˌsaiˈtəusis]

释义

遗传性球形红细胞性贫血；

权威例句

Hereditary Spherocytosis
Hereditary Spherocytosis
Hereditary spherocytosis.
HEREDITARY SPHEROCYTOSIS; CLINICAL FAMILY STUDIES.
Hereditary spherocytosis associated with deletion of human erythrocyte ankyrin gene on chromosome 8
Hereditary spherocytosis--defects in proteins that connect the membrane skeleton to the lipid bilayer
Hereditary spherocytosis, thrombocytosis, and chronic pulmonary emboli: a case report and review of the literature.
Partial deficiency of erythrocyte spectrin in hereditary spherocytosis
Guidelines for the diagnosis and management of hereditary spherocytosis.
Fine structure of the red pulp of the spleen in hereditary spherocytosis
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosis.
PARENTAL MOSAICISM FOR ANKYRIN-1 MUTATIONS IN TWO FAMILIES WITH HEREDITARY SPHEROCYTOSIS (HS)
Characterization of the underlying molecular defect in hereditary spherocytosis associated with spectrin deficiency.