Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases
出版年份 2011 全文链接
标题
Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases
作者
关键词
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出版物
PRENATAL DIAGNOSIS
Volume 31, Issue 13, Pages 1270-1282
出版商
Wiley
发表日期
2011-10-28
DOI
10.1002/pd.2884
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?
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- Analytical and clinical validity of whole-genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay
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- Clinical variability of the 22q11.2 duplication syndrome
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- Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives
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- Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes
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- Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases
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