CORPORATE CONTENT MANAGEMENT AND DELIVERY SYSTEM von MEYER, KIP, L, RAUEN, PHILIP, J., IV, KEANE, PAUL, L, BJORNSON, CHRISTOPHER, W, HOUCK, DAVID, M, MODRUSON, FRANK, B, HARTSHORN, LANCE, P

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CORPORATE CONTENT MANAGEMENT AND DELIVERY SYSTEM von MEYER, KIP, L, RAUEN, PHILIP, J., IV, KEANE, PAUL, L, BJORNSON, CHRISTOPHER, W, HOUCK, DAVID, M, MODRUSON, FRANK, B, HARTSHORN, LANCE, P

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CORPORATE CONTENT MANAGEMENT AND DELIVERY SYSTEM von MEYER, KIP, L, RAUEN, PHILIP, J., IV, KEANE, PAUL, L, BJORNSON, CHRISTOPHER, W, HOUCK, DAVID, M, MODRUSON, FRANK, B, HARTSHORN, LANCE, P

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CORPORATE CONTENT MANAGEMENT AND DELIVERY SYSTEM von KIP, L. MEYER, LANCE, P. HARTSHORN, CHRISTOPHER, W. BJORNSON, DAVID, M. HOUCK, PHILIP, J., IV RAUEN, PAUL, L. KEANE, FRANK, B. MODRUSON

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CORPORATE CONTENT MANAGEMENT AND DELIVERY SYSTEM von MEYER, KIP, L, RAUEN, PHILIP, J., IV, KEANE, PAUL, L, BJORNSON, CHRISTOPHER, W, HOUCK, DAVID, M, MODRUSON, FRANK, B, HARTSHORN, LANCE, P

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Corporate content management and delivery system von HOUCK DAVID MILES, KEANE PAUL L, RAUEN PHILIP JOSEPH, BJORNSON CHRISTOPHER W, HARTSHORN LANCE PATRICK, MEYER KIP LEONARD, MODRUSON FRANK B

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Haplotyping germline and cancer genomes with high-throughput linked-read sequencing von Zheng, Grace X Y, Lau, Billy T, Schnall-Levin, Michael, Jarosz, Mirna, Bell, John M, Hindson, Christopher M, Kyriazopoulou-Panagiotopoulou, Sofia, Masquelier, Donald A, Merrill, Landon, Terry, Jessica M, Mudivarti, Patrice A, Wyatt, Paul W, Bharadwaj, Rajiv, Makarewicz, Anthony J, Li, Yuan, Belgrader, Phillip, Price, Andrew D, Lowe, Adam J, Marks, Patrick, Vurens, Gerard M, Hardenbol, Paul, Montesclaros, Luz, Luo, Melissa, Greenfield, Lawrence, Wong, Alexander, Birch, David E, Short, Steven W, Bjornson, Keith P, Patel, Pranav, Hopmans, Erik S, Wood, Christina, Kaur, Sukhvinder, Lockwood, Glenn K, Stafford, David, Delaney, Joshua P, Wu, Indira, Ordonez, Heather S, Grimes, Susan M, Greer, Stephanie, Lee, Josephine Y, Belhocine, Kamila, Giorda, Kristina M, Heaton, William H, McDermott, Geoffrey P, Bent, Zachary W, Meschi, Francesca, Kondov, Nikola O, Wilson, Ryan, Bernate, Jorge A, Gauby, Shawn, Kindwall, Alex, Bermejo, Clara, Fehr, Adrian N, Chan, Adrian, Saxonov, Serge, Ness, Kevin D, Hindson, Benjamin J, Ji, Hanlee P

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Lineage of origin in rhabdomyosarcoma informs pharmacological response von Abraham, Jinu, Nuñez-Álvarez, Yaiza, Hettmer, Simone, Carrió, Elvira, Chen, Hung-I Harry, Nishijo, Koichi, Huang, Elaine T, Prajapati, Suresh I, Walker, Robert L, Davis, Sean, Rebeles, Jennifer, Wiebush, Hunter, McCleish, Amanda T, Hampton, Sheila T, Bjornson, Christopher R R, Brack, Andrew S, Wagers, Amy J, Rando, Thomas A, Capecchi, Mario R, Marini, Frank C, Ehler, Benjamin R, Zarzabal, Lee Ann, Goros, Martin W, Michalek, Joel E, Meltzer, Paul S, Langenau, David M, LeGallo, Robin D, Mansoor, Atiya, Chen, Yidong, Suelves, Mònica, Rubin, Brian P, Keller, Charles

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Demographic history and rare allele sharing among human populations von Gravel, Simon, Henn, Brenna M, Gutenkunst, Ryan N, Indap, Amit R, Marth, Gabor T, Clark, Andrew G, Yu, Fuli, Gibbs, Richard A, Bustamante, Carlos D

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Haplotyping germline and cancer genomes using high-throughput linked-read sequencing von Zheng, Grace X.Y., Lau, Billy T., Schnall-Levin, Michael, Jarosz, Mirna, Bell, John M., Hindson, Christopher M., Kyriazopoulou-Panagiotopoulou, Sofia, Masquelier, Donald A., Merrill, Landon, Terry, Jessica M., Mudivarti, Patrice A., Wyatt, Paul W., Bharadwaj, Rajiv, Makarewicz, Anthony J., Li, Yuan, Belgrader, Phillip, Price, Andrew D., Lowe, Adam J., Marks, Patrick, Vurens, Gerard M., Hardenbol, Paul, Montesclaros, Luz, Luo, Melissa, Greenfield, Lawrence, Wong, Alexander, Birch, David E., Short, Steven W., Bjornson, Keith P., Patel, Pranav, Hopmans, Erik S., Wood, Christina, Kaur, Sukhvinder, Lockwood, Glenn K., Stafford, David, Delaney, Joshua P., Wu, Indira, Ordonez, Heather S., Grimes, Susan M., Greer, Stephanie, Lee, Josephine Y., Belhocine, Kamila, Giorda, Kristina M., Heaton, William H., McDermott, Geoffrey P., Bent, Zachary W., Meschi, Francesca, Kondov, Nikola O., Wilson, Ryan, Bernate, Jorge A., Gauby, Shawn, Kindwall, Alex, Bermejo, Clara, Fehr, Adrian N., Chan, Adrian, Saxonov, Serge, Ness, Kevin D., Hindson, Benjamin J., Ji, Hanlee P.

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Conscious visual abilities in a patient with early bilateral occipital damage von Giaschi, D., Bjornson, B., Jan, J., Tata, M., Young, S. A., Lyons, C. J., Good, W. V., Wong, P. K. H.

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Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands von Jin, Sheng Chih, Homsy, Jason, Zaidi, Samir, Lu, Qiongshi, Morton, Sarah, DePalma, Steven R, Zeng, Xue, Qi, Hongjian, Chang, Weni, Sierant, Michael C, Hung, Wei-Chien, Haider, Shozeb, Zhang, Junhui, Knight, James, Bjornson, Robert D, Castaldi, Christopher, Tikhonoa, Irina R, Bilguvar, Kaya, Mane, Shrikant M, Sanders, Stephan J, Mital, Seema, Russell, Mark, Gaynor, William, Deanfield, John, Giardini, Alessandro, Porter, George A, Srivastava, Deepak, Lo, Cecelia W, Shen, Yufeng, Watkins, W. Scott, Yandell, Mark, Yost, H. Joseph, Tristani-Firouzi, Martin, Newburger, Jane W, Roberts, Amy E, Kim, Richard, Zhao, Hongyu, Kaltman, Jonathan R, Goldmuntz, Elizabeth, Chung, Wendy K, Seidman, Jonathan G, Gelb, Bruce D, Seidman, Christine E, Lifton, Richard P, Brueckner, Martina

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