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

学习怎么用

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.

单词	hereditary spherocytosis
释义	hereditary spherocytosis 听听怎么读 [hi?redit?ri ?sfi?r??sai?t?usis] 是什么意思释义遗传性球形红细胞性贫血；学习怎么用权威例句 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.
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