prenatal molecular diagnosis

基本解釋

Objective To carry out prenatal molecular diagnosis on 3 fetuses from different pedigrees with X-linked adrenoleukodystrophy (ALD).
目的對3名來自不同家系的腎上腺腦白質(zhì)營養(yǎng)不良（ALD）攜帶者所懷胎兒進行產(chǎn)前分子診斷。
Conclusion This was the first time that CLS was diagnosed by molecular method in China, which provided a genetic basis for gene diagnosis and prenatal diagnosis of CLS.
結(jié)論本研究是國內(nèi)首次在分子水平確診CLS患者，為CLS的基因診斷和產(chǎn)前診斷提供遺傳基礎(chǔ)。
jcyxylc.pumc.edu.cn
Objective: To establish a new, rapid and clinical practical molecular cytogenetic method for diagnosing the chromosomal diseases as well as guiding aristogenesis and prenatal diagnosis.
目的：建立臨床實用的快速檢出染色體病新的分子細胞遺傳學(xué)方法，為指導(dǎo)優(yōu)生優(yōu)育和產(chǎn)前診斷工作提供可運行的實驗檢測手段。