elliptocytosis
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英式音标:[ɪlɪptəsaɪ'təʊsɪs]

美式音标:[ɪlɪptəsaɪ'toʊsɪs]

词汇分类:血液系统与免疫学(百歌医学单词USMLE),医学英语词汇大集合,医学英语长难词语
词义:
n.
椭圆(形)红细胞增多症,椭圆(形)红细胞性贫血;椭圆形;
用法:
elliptocytosis
ELLIPTOCYTOSIS
The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins ...
Molecular basis for elliptocytosis associated with glycophorin C and D deficiency in the Leach phenotype
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stab...
Hereditary elliptocytosis: spectrin and protein 4.1R
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin.
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental...
Hereditary elliptocytosis and related disorders
Defective Spectrin Dimer-Dimer Association in Hereditary Elliptocytosis
An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).
权威例句
Elliptocytosis.elliptocytosis
ELLIPTOCYTOSIS
The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type
Molecular analysis of insertion/deletion mutations in protein 4.1 in elliptocytosis. II. Determination of molecular genetic origins ...
Molecular basis for elliptocytosis associated with glycophorin C and D deficiency in the Leach phenotype
Deficiency of skeletal membrane protein band 4.1 in homozygous hereditary elliptocytosis. Implications for erythrocyte membrane stab...
Hereditary elliptocytosis: spectrin and protein 4.1R
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in Benin.
FACL4, a new gene encoding long-chain acyl-CoA synthetase 4, is deleted in a family with Alport syndrome, elliptocytosis, and mental...
Hereditary elliptocytosis and related disorders
Defective Spectrin Dimer-Dimer Association in Hereditary Elliptocytosis
An insertional frameshift mutation of the beta-spectrin gene associated with elliptocytosis in spectrin nice (beta 220/216).
造句:
1. Create a subdirectory for each database, to store the backup files.
为每个数据库创建子目录以便存储备份文件.
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2. Leave blank or enter a subdirectory off the root.
留空或输入一个子目录了根.
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3. The directory is not a subdirectory of the root directory.
目录不是根目录下的子目录.
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4. Each directory Rongbu Xia , further subdivided into a subdirectory.
每个目录容不下时, 再细分成子目录.
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5. The file name for the extension may not include subdirectory elements.
扩展的文件名不能包含子目录元素.
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[ subdirectory 造句 ]
elliptocytosis
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