The Farmer in England, 1650–1980, edited by Richard W.Hoyle, Farnham, England: Ashgate, 2013. 366 pp. $144.95 (cloth). ISBN: 978‐1‐4724‐0584‐5 von Lonie, Jean

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Outcomes of international travel on agriculture: agricultural leadership programs create transformative learning and behavior change in farmers and ranchers von Friedrichsen, Claire N., Lonie, Jean, Haberstroh, Melissa D., Hejny, Terence A.

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Student Perceptions of the Impact of their Diverse Study Abroad Experiences von Harrell, Alison, Sterner, Glenn, Alter, Theodore R., Lonie, Jean

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The Farmer in England, 1650–1980, edited by Richard W. Hoyle, Farnham, England: Ashgate, 2013. 366 pp. $144.95 (cloth). ISBN: 978‐1‐4724‐0584‐5 von Lonie, Jean

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Book Review - The Farmer in England, 1650-1980 von Lonie, Jean

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The Farmer in England, 1650-1980 - Edited by Richard W. Hoyle von Lonie, Jean

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LIQUID SAMPLING COLLECTORS von PETER JAMES THOMPSON, SUSAN JEAN LONIE

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Sampling from liquid - liquid extraction columns von PETER JAMES THOMPSON, SUSAN JEAN LONIE

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COLLECTEUR POUR ECHANTILLONNER DU LIQUIDE DANS UNE COLONNE D'EXTRACTION LIQUIDE/LIQUIDE von SUSAN JEAN LONIE ET PETER JAMES THOMPSON

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Liquid - liquid extraction columns von LONIE, SUSAN JEAN

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Liquid-liquid extraction columns von WILLIAM BATEY, PETER JAMES THOMPSON, JOHN DESMOND THORNTON, SUSAN JEAN LONIE

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COLLECTEUR POUR ECHANTILLONNER DU LIQUIDE DANS UNE COLONNE D'EXTRACTION LIQUIDE/LIQUIDE von SUSAN JEAN LONIE ET PETER JAMES THOMPSON

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A blood atlas of COVID-19 defines hallmarks of disease severity and specificity von Ai, Zhichao, Ainsworth, Mark, Arancibia-Cárcamo, Carolina V., Attar, Moustafa, Baillie, J. Kenneth, Bashford-Rogers, Rachael, Bicanic, Tihana, Bowness, Paul, Brent, Andrew, Buck, David, Camara, Susana, Clutterbuck, Elizabeth A., Coles, Mark, Conlon, Christopher P., Cribbs, Adam P., Curion, Fabiola, Davenport, Emma E., Davidson, Neil, Davis, Simon, Dendrou, Calliope A., Dequaire, Julie, Docker, James, Dold, Christina, Downes, Damien, Drakesmith, Hal, Dunachie, Susanna J., Espinosa, Alexis, Felle, Sally, Fernandez Mendoza, Maria, Forrow, Aden, Frater, John, Fries, Anastasia, Garner, Lucy C., Godfrey, Leila, Gomez Vazquez, Maria, Green, Angie, Harper, Hong, Heilig, Raphael, Hester, Svenja, Hill, Jennifer, Hinds, Charles, Hird, Clare, Hutton, Paula, Jainarayanan, Ashwin, Jansen, Kathrin, Jones, Elizabeth, Klenerman, Paul, Knight, Julian C., Kumar Sharma, Piyush, Kurupati, Prathiba, Kwok, Andrew, Lee, Angela, Lonie, Lorne, Luo, Jian, Marsden, Brian, Martinez, Jose, Matthews, Philippa C., Mazurczyk, Michalina, McGowan, Simon, Mi, Yuxin, Montadon, Ruddy, O'Brien, Darragh P., Ogg, Graham, Overend, Lauren, Pereira Pinho, Mariana, Perez, Elena, Pollard, Andrew J., Quan, T. Phuong, Revale, Santiago, Silva-Reyes, Laura, Richard, Jean-Baptiste, Rich-Griffin, Charlotte, Salio, Mariolina, Sansom, Stephen Nicholas, Sauka-Spengler, Tatjana, Schwessinger, Ron, Sobrinodiaz, Alberto, Stockdale, Lisa, Strickland, Marie, Sun, Bo, Taylor, Chelsea, Taylor, Stephen, Taylor, Adan, Tomic, Adriana, Tong, Orion, Trebes, Amy, Uhlig, Holm, van Grinsven, Erinke, Vendrell, Iolanda, Verheul, Marije, Wang, Guanlin, Wang, Lihui, Wang, Dapeng, Watkinson, Peter, Watson, Robert, Witty, Lorna, Wray, Katherine, Xue, Luzheng, Young, Rebecca K., Zhang, Ping

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Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis von Sharma, Vikram P, Fenwick, Aimée L, Brockop, Mia S, McGowan, Simon J, Goos, Jacqueline A C, Hoogeboom, A Jeannette M, Brady, Angela F, Jeelani, Nu Owase, Lynch, Sally Ann, Mulliken, John B, Murray, Dylan J, Phipps, Julie M, Sweeney, Elizabeth, Tomkins, Susan E, Wilson, Louise C, Bennett, Sophia, Cornall, Richard J, Broxholme, John, Kanapin, Alexander, Johnson, David, Wall, Steven A, van der Spek, Peter J, Mathijssen, Irene M J, Maxson, Robert E, Twigg, Stephen R F, Wilkie, Andrew O M

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Application of whole genome and RNA sequencing to investigate the genomic landscape of common variable immunodeficiency disorders von van Schouwenburg, Pauline A, Davenport, Emma E, Kienzler, Anne-Kathrin, Marwah, Ishita, Wright, Benjamin, Lucas, Mary, Malinauskas, Tomas, Martin, Hilary C, Lockstone, Helen E, Cazier, Jean-Baptiste, Chapel, Helen M, Knight, Julian C, Patel, Smita Y

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Whole-genome sequencing of bladder cancers reveals somatic CDKN1A mutations and clinicopathological associations with mutation burden von Cazier, J. -B., Rao, S. R., McLean, C. M., Walker, A. K., Wright, B. J., Jaeger, E. E. M., Kartsonaki, C., Marsden, L., Yau, C., Camps, C., Kaisaki, P., Taylor, J., Catto, J. W., Tomlinson, I. P. M., Kiltie, A. E., Hamdy, F. C.

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Congenital myasthenic syndromes due to mutations in ALG2 and ALG14 von COSSINS, Judith, BELAYA, Katsiaryna, LAVAL, Steven, ZAIN SEIDHAMED, Mohammed, DONNELLY, Peter, BENTLEY, David, MCGOWAN, Simon J, MÜLLER, Juliane, PALACE, Jacqueline, LOCHMÜLLER, Hanns, BEESON, David, HICKS, Debbie, SALIH, Mustafa A, FINLAYSON, Sarah, CARBONI, Nicola, WEI WEI LIU, MAXWELL, Susan, ZOLTOWSKA, Katarzyna, TORABI FARSANI, Golara

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Open Data, Open Source and Open Standards in chemistry: The Blue Obelisk five years on von O'Boyle, Noel M, Guha, Rajarshi, Willighagen, Egon L, Adams, Samuel E, Alvarsson, Jonathan, Bradley, Jean-Claude, Filippov, Igor V, Hanson, Robert M, Hanwell, Marcus D, Hutchison, Geoffrey R, James, Craig A, Jeliazkova, Nina, Lang, Andrew SID, Langner, Karol M, Lonie, David C, Lowe, Daniel M, Pansanel, Jérôme, Pavlov, Dmitry, Spjuth, Ola, Steinbeck, Christoph, Tenderholt, Adam L, Theisen, Kevin J, Murray-Rust, Peter

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Gain-of-Function Mutations in ZIC1 Are Associated with Coronal Craniosynostosis and Learning Disability von Twigg, Stephen R.F., Forecki, Jennifer, Goos, Jacqueline A.C., Richardson, Ivy C.A., Hoogeboom, A. Jeannette M., van den Ouweland, Ans M.W., Swagemakers, Sigrid M.A., Lequin, Maarten H., Van Antwerp, Daniel, McGowan, Simon J., Westbury, Isabelle, Miller, Kerry A., Wall, Steven A., van der Spek, Peter J., Mathijssen, Irene M.J., Pauws, Erwin, Merzdorf, Christa S., Wilkie, Andrew O.M.

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Homozygous mutations in a predicted endonuclease are a novel cause of congenital dyserythropoietic anemia type I von Babbs, C., Roberts, N. A., Sanchez-Pulido, L., McGowan, S. J., Ahmed, M. R., Brown, J. M., Sabry, M. A., Bentley, D. R., McVean, G. A., Donnelly, P., Gileadi, O., Ponting, C. P., Higgs, D. R., Buckle, V. J.

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