Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01687.x/fullpdf
Reference60 articles.
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