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Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data

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Description scientific article
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author: Steven R DePalma  Joseph Glessner  Bruce D. Gelb  Martina Brueckner  Erica Mazaika  Jeremy Leipzig  Ryan Golhar  Alexander G. Bick  Jason Homsy  Jonathan R Kaltman  Jonathan G Seidman  Elizabeth Goldmuntz  Christine E. Seidman  Dorothy Warburton  Stephan J. Sanders  Hakon Hakonarson 

Publication date September 9, 2014
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