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1)  Léri-Weill syndrome
Lri-Weill综合征
1.
It has now been confirmed that the human SHOX gene mutation can cause Léri-Weill syndrome,Turner syndrome,idiopathic short stature growth and its related characteristic skeletal deformities.
现已证实,人类SHOX基因突变与Lri-Weill综合征、Turner综合征及特发性矮小的生长障碍及特征性骨骼畸形有关。
2)  Weill-Marchesani syndrome
Weill-Marchesani综合征
1.
Therapeutic effect analysis of Weill-Marchesani syndrome;
Weill-Marchesani综合征3例疗效分析
2.
Weill-Marchesani syndrome:a case report;
Weill-Marchesani综合征
3)  POEMS syndrome
POEMS综合征
1.
Clinical Analysis of 5 Cases of POEMS Syndrome;
POEMS综合征5例临床分析
2.
Clinical manifestations and diagnosis of POEMS syndrome;
POEMS综合征的临床表现及诊断
3.
Clinical analysis of misdiagnosis of patients with POEMS syndrome;
POEMS综合征临床误诊原因分析
4)  Turner syndrome
Turner综合征
1.
Karyotypes and pelvic ultrasonography in children with Turner syndrome;
Turner综合征患儿染色体核型和盆腔超声的分析
2.
Effects of recombinant human growth hormone on height in Turner syndrome.;
生长激素对Turner综合征的促身高作用
3.
Marker chromosome analysis in Chinese patients with Turner syndrome by fluorescence in situ hybridization;
Turner综合征患儿标记染色体的来源研究
5)  Tourette's syndrome
Tourette综合征
1.
Study on the character of auditory P300 of Tourette's syndrome with or without behavioral problems;
Tourette综合征伴或不伴行为问题的P300研究
6)  Mirizzi syndrome
Mirizzi综合征
1.
The clinical analysis of diagnosis and laparoscopic treatment 37cases with Mirizzi syndrome;
Mirizzi综合征的诊断及腹腔镜治疗的临床分析(附37例报告)
2.
Diagnosis and treatment of 53 patients with Mirizzi syndrome;
Mirizzi综合征诊治分析53例
3.
Diagnosis and treatment of 14 patients with Mirizzi syndrome;
Mirizzi综合征诊治14例
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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