英语词汇“spherocytosis”的意思、用法、释义、翻译、读音、例句、短语、词组-英语词典

是什么意思

球形红细胞（贫血）症；

英英释义

Spherocytosis

Spherocytosis is an auto-hemolytic anemia (a disease of the blood) characterized by the production of red blood cells (RBCs), or erythrocytes, that are sphere-shaped, rather than bi-concave disk shaped. Spherocytes are found in hereditary spherocytosis and autoimmune hemolytic anemia.

以上来源于:Wikipedia

学习怎么用

权威例句

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.
Fine structure of the red pulp of the spleen in hereditary spherocytosis
Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update.
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 (Abstract #1856)
Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.

单词	spherocytosis
释义	spherocytosis 听听怎么读英 ['sf??r??sa?'t??s?s] 美 ['sf??r??sa?'to?s?s] 是什么意思 n. 球形红细胞（贫血）症；英英释义 Spherocytosis Spherocytosis is an auto-hemolytic anemia (a disease of the blood) characterized by the production of red blood cells (RBCs), or erythrocytes, that are sphere-shaped, rather than bi-concave disk shaped. Spherocytes are found in hereditary spherocytosis and autoimmune hemolytic anemia. 以上来源于:Wikipedia 学习怎么用权威例句 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. Fine structure of the red pulp of the spleen in hereditary spherocytosis Guidelines for the diagnosis and management of hereditary spherocytosis--2011 update. 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 (Abstract #1856) Coinheritance of Gilbert syndrome increases the risk for developing gallstones in patients with hereditary spherocytosis.
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