Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data (Q30849515)
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| English | 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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Increased frequency of de novo copy number variants in congenital heart disease by integrative analysis of single nucleotide polymorphism array and exome sequence data (English)
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Jeremy Leipzig
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Hakon Hakonarson
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Elizabeth Goldmuntz
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Dorothy Warburton
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Christine Seidman
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Joseph T Glessner
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Jonathan R Kaltman
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Martina Brueckner
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Jonathan Seidman
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Jason Homsy
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Ryan Golhar
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Steven R DePalma
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Alexander G Bick
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Bruce D Gelb
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Erica Mazaika
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Menachem Fromer
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Kaoru Ito
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Laura Rodriguez-Murillo
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Badri Vardarajan
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Michael Italia
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Boris Yamrom
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Michael Ronemus
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Ivan Iossifov
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A Jeremy Willsey
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Matthew W State
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Peter S White
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Yufeng Shen
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Richard Lifton
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Wendy K Chung
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9 September 2014
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115
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884-896
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