| 释义 |
adrenoleukodystrophy 英ædrɪnəʊluːkəʊ'dɪstrəʊfɪ美ædrɪnəʊluːkəʊ'dɪstrəʊfɪ COCA²⁵⁴³³⁷⁺⁶BNC²³⁶²¹³⁺¹
基本例句
脑白质肾上腺萎缩症¹⁰⁰
Conclusion: Mutations of ALD gene is the causes of X- linked recessive adrenoleukodystrophy in Chinese population.
结论ALD基因突变是中国人 X-连锁隐性遗传 ALD发病原因之一。 cnki
The molecular diagnosis for X linked adrenoleukodystrophyALD using mutational analysis at genomic DNA level is important.
在基因组 DNA水平，应用基因突变分析的方法对肾上腺脑白质营养不良进行分子诊断十分重要。 cnki
Objective To analyze the ABCD1 gene mutations in5 cases of X- linked adrenoleukodystrophy X- ALD patients and2 cases of their mothers.
目的对5例 X-连锁肾上腺脑白质营养不良 X- ALD患儿及其中2例的母亲进行 ABCD1基因突变分析。 cnki
Objective To carry out prenatal molecular diagnosis on3 fetuses from different pedigrees with X-linked adrenoleukodystrophy ALD.
目的对3名来自不同家系的肾上腺脑白质营养不良 ALD携带者所怀胎儿进行产前分子诊断。 cnki
Objective To identity the ABCD1 gene mutation in a Chinese family with X-linked adrenoleukodystrophyALD.
目的鉴定并分析1个新的肾上腺脑白质营养不良家系的基因突变类型和位点。 cnki
Objective To investigate the typical clinical manifestations, biochemical change and treatment of X- linked adrenoleukodystrophy.
目的：研究 X-连锁肾上腺脑白质营养不良的临床、生化改变及治疗情况。 dictall
Objective To study the pathology, clinical symptomatology and MRI findings of adrenoleukodystrophy.
目的：探讨肾上腺泉脑白质营养不良的病理、临床及 MRI表现。 cnki |