Increased Frequency of De Novo Copy Number Variations in Congenital Heart Disease by Integrative Analysis of SNP Array and Exome Sequence Data

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Veröffentlicht in:Circulation research 2014-09, Vol.115 (10), p.884-896
Hauptverfasser: Glessner, Joseph T., Bick, Alexander G., Ito, Kaoru, Homsy, Jason, Rodriguez-Murillo, Laura, Fromer, Menachem, Mazaika, Erica, Vardarajan, Badri, Italia, Michael, Leipzig, Jeremy, DePalma, Steven R., Golhar, Ryan, Sanders, Stephan J., Yamrom, Boris, Ronemus, Michael, Iossifov, Ivan, Willsey, A. Jeremy, State, Matthew W., Kaltman, Jonathan R., White, Peter S., Shen, Yufeng, Warburton, Dorothy, Brueckner, Martina, Seidman, Christine, Goldmuntz, Elizabeth, Gelb, Bruce D., Lifton, Richard, Seidman, Jonathan, Hakonarson, Hakon, Chung, Wendy K.
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container_end_page 896
container_issue 10
container_start_page 884
container_title Circulation research
container_volume 115
creator Glessner, Joseph T.
Bick, Alexander G.
Ito, Kaoru
Homsy, Jason
Rodriguez-Murillo, Laura
Fromer, Menachem
Mazaika, Erica
Vardarajan, Badri
Italia, Michael
Leipzig, Jeremy
DePalma, Steven R.
Golhar, Ryan
Sanders, Stephan J.
Yamrom, Boris
Ronemus, Michael
Iossifov, Ivan
Willsey, A. Jeremy
State, Matthew W.
Kaltman, Jonathan R.
White, Peter S.
Shen, Yufeng
Warburton, Dorothy
Brueckner, Martina
Seidman, Christine
Goldmuntz, Elizabeth
Gelb, Bruce D.
Lifton, Richard
Seidman, Jonathan
Hakonarson, Hakon
Chung, Wendy K.
description
doi_str_mv 10.1161/CIRCRESAHA.115.304458
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title Increased Frequency of De Novo Copy Number Variations in Congenital Heart Disease by Integrative Analysis of SNP Array and Exome Sequence Data
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