产前诊断
医学诊断
核型
医学
产科
遗传学
生物
怀孕
染色体
病理
胎儿
基因
作者
Diana Wellesley,Anneke Lucassen
出处
期刊:Archives of Disease in Childhood-fetal and Neonatal Edition
[BMJ]
日期:2014-05-03
卷期号:99 (4): F338-F341
被引量:4
标识
DOI:10.1136/archdischild-2013-304835
摘要
Prenatal array comparative genome hybridisation (aCGH) testing has by and large replaced routine karyotyping in many healthcare settings. While this will lead to more diagnoses, uncertain, unexpected or unhelpful findings are also likely to increase. This is the case for aCGH in any setting, but we discuss the particular challenges the prenatal setting generates and suggest areas that need further debate and discussion as well as some pragmatic ways forward.
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