Facioscapulohumeral是什么意思_Facioscapulohumeral的中文翻译|音标|读音|用法|短语例句|近反义词

双语例句

1、

Diagnosis of facioscapulohumeral muscular dystrophy using double enzyme digestion associated Southern blotting method

应用双酶切/Southern杂交方法诊断面肩肱型肌营养不良

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2、

Progress in researches on the molecular genetics of facioscapulohumeral muscular dystrophy

面肩肱型肌营养不良症的分子遗传学研究进展

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3、

Objective To perform gene diagnosis and summarize clinical features of facioscapulohumeral muscular dystrophy ( FSHD) in order to improve its diagnosis.

目的对面肩肱型肌营养不良症（FSHD）患者进行基因诊断并总结其临床特征，以提高FSHD的诊断水平。

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4、

Facioscapulohumeral muscular dystrophy ( FSHD) is a kind of progressive muscular disorder. It often occurs before 30 years old The face is initially involved, then the shoulder girdle, and finally the pelvic muscles Asymmetry of weakness is not unusual.

面肩肱型肌营养不良症（FSHD）是一种进行肌肉疾病，多于30岁以前发病，面肌总有受累；然后是肩肿带肌，能后是盆带肌等的萎缩和力弱。

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5、

Establishment of Pulsed Field Gel Electrophoresis System and Study on the Gene Structure of Facioscapulohumeral Muscular Dystrophy in Chinese Population

脉冲电场凝胶电泳技术体系的建立与中国人面肩肱型肌营养不良症的基因分析

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6、

Mechanism of translocation between chromosomes 4q and 10q in facioscapulohumeral muscular dystrophy

面肩肱型肌营养不良症患者染色体4q-10q相互易位机制的初步研究

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7、

Gene diagnosis of facioscapulohumeral muscular dystrophy

面肩肱型肌营养不良症基因诊断

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8、

Two patients were diagnosed as facioscapulohumeral muscular dystrophy, one as limb-girdle muscular dystrophy and the others' etiology were unknown.

其中2例临床诊断为面肩肱型肌营养不良，1例免疫组化染色证实为肢带型肌营养不良，余均未发现明确病因。

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9、

The FacioScapuloHumeral Muscular Dystrophy Society addresses issues and needs related to this disease of the skeletal muscle, which is a type of muscular dystrophy.

面部肩胛部肱部肌肉萎缩学会：强调与此骨骼肌疾病（肌肉萎缩其中一种类型）相关的议题与需求。

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10、

Study on characteristics of gene structure and gene diagnosis of facioscapulohumeral muscular dystrophy using pulse field gel electrophoresis

应用脉冲场电泳技术研究面肩肱型肌营养不良症的基因突变特征及进行基因诊断

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11、

Application of the Bgl ⅱ-Bln ⅰ dosage test to gene diagnosis of facioscapulohumeral muscular dystrophy 1A gene

BglⅡ-BlnⅠ剂量检测方法在面肩肱型肌营养不良症1A基因诊断中的应用

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12、

Objective To explore the genotype-phenotype correlation of facioscapulohumeral muscular dystrophy ( FSHD) 1A gene.

目的探讨面肩肱型肌营养不良症（FSHD）1A的基因型与临床表型之间的相关关系。

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相关词组

Facioscapulohumeral muscular dystrophy性肌肉萎缩症；面肩胛肱型肌营养不良症；面肩肱肌营养不良；肱型肌营养不良症；面肩肱型肌营养不良症

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