New spaces – new pedagogies: Implementing personalised learning in primary school innovative learning environments von Cardno, Carol, Tolmie, Emma, Howse, Jo

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New spaces - new pedagogies: Implementing personalised learning in primary school innovative learning environments von Carol Cardno, Emma Tolmie, Jo Howse

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New spaces - new pedagogies: Implementing personalised learning in primary school innovative learning environments von Carol Cardno, Emma Tolmie, Jo Howse

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Implementing personalised learning in New Zealand primary schools Innovative Learning Environments von Tolmie, Emma

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New spaces, new pedagogies : implementing personalized learning in primary school innovative learning environments von Cardno, Carol E. M, Tolmie, Emma, Howse, Jo

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Robotic-Assisted Surgery for Rectal Cancer: An Expedited Summary of the Clinical Evidence von Ontario Health

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Fractional Exhaled Nitric Oxide Testing for the Diagnosis and Management of Asthma: a Health Technology Assessment

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Moving from the past into the future with new spaces and new pedagogies von Howse, Jo, Tolmie, Emma

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Mosaic structural variation in children with developmental disorders von King, Daniel A, Jones, Wendy D, Crow, Yanick J, Dominiczak, Anna F, Foster, Nicola A, Gaunt, Tom R, Harris, Jade, Hellens, Stephen W, Homfray, Tessa, Innes, Josie, Jones, Elizabeth A, Joss, Shelagh, Kulkarni, Abhijit, Mansour, Sahar, Morris, Andrew D, Parker, Michael J, Porteous, David J, Shihab, Hashem A, Smith, Blair H, Tatton-Brown, Katrina, Tolmie, John L, Trzaskowski, Maciej, Vasudevan, Pradeep C, Wakeling, Emma, Wright, Michael, Plomin, Robert, Timpson, Nicholas J, Hurles, Matthew E

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Social effects of collaborative learning in primary schools von Tolmie, Andrew Kenneth, Topping, Keith J., Christie, Donald, Donaldson, Caroline, Howe, Christine, Jessiman, Emma, Livingston, Kay, Thurston, Allen

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Group work in elementary science: Towards organisational principles for supporting pupil learning von Howe, Christine, Tolmie, Andy, Thurston, Allen, Topping, Keith, Christie, Donald, Livingston, Kay, Jessiman, Emma, Donaldson, Caroline

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Targeted methylation testing of a patient cohort broadens the epigenetic and clinical description of imprinting disorders von Poole, Rebecca L., Docherty, Louise E., Al Sayegh, Abeer, Caliebe, Almuth, Turner, Claire, Baple, Emma, Wakeling, Emma, Harrison, Lucy, Lehmann, Anna, Temple, I. Karen, Mackay, Deborah J.G.

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How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum von BANKA, Siddharth, VEERAMACHANENI, Ratna, METCALFE, Kay, CHANDLER, Kate, MAGEE, Alex, STEWART, Fiona, MCCONNELL, Vivienne Pm, DONNELLY, Deirdre E, BERLAND, Siren, HOUGE, Gunnar, MORTON, Jenny E, OLEY, Christine, REARDON, William, REVENCU, Nicole, PARK, Soo-Mi, DAVIES, Sally J, FRY, Andrew E, ANN LYNCH, Sally, GILL, Harinder, SCHWEIGER, Susann, LAM, Wayne Wk, TOLMIE, John, MOHAMMED, Shehla N, HOWARD, Emma, HOBSON, Emma, SMITH, Audrey, BLYTH, Moira, BENNETT, Christopher, VASUDEVAN, Pradeep C, GARCIA-MINAUR, Sixto, HENDERSON, Alex, GOODSHIP, Judith, WRIGHT, Michael J, FISHER, Richard, BUNSTONE, Sancha, GIBBONS, Richard, PRICE, Susan M, DE SILVA, Deepthi C, KAREN TEMPLE, I, COLLINS, Amanda L, LACHLAN, Katherine, ELMSLIE, Frances, MCENTAGART, Meriel, CASTLE, Bruce, CLAYTON-SMITH, Jill, RAGGE, Nicola, BLACK, Graeme C, DONNAI, Dian, PARKER, Michael J, CROW, Yanick J, KERR, Bronwyn, KINGSTON, Helen

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WT1 mutations in Meacham syndrome suggest a coelomic mesothelial origin of the cardiac and diaphragmatic malformations von Suri, Mohnish, Kelehan, Peter, O'Neill, David, Vadeyar, Shantala, Grant, Judith, Ahmed, S. Faisal, Tolmie, John, McCann, Emma, Lam, Wayne, Smith, Shirley, FitzPatrick, David, Hastie, Nicholas D., Reardon, William

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What Can the Study of Genetics Offer to Educators? von Thomas, Michael S. C., Kovas, Yulia, Meaburn, Emma L., Tolmie, Andrew

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Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA von van Kogelenberg, Margriet, Clark, Alice R., Jenkins, Zandra, Morgan, Tim, Anandan, Ananda, Sawyer, Gregory M., Edwards, Matthew, Dudding, Tracy, Homfray, Tessa, Castle, Bruce, Tolmie, John, Stewart, Fiona, Kivuva, Emma, Pilz, Daniela T., Gabbett, Michael, Sutherland-Smith, Andrew J., Robertson, Stephen P.

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Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling von Rice, Gillian I, del Toro Duany, Yoandris, Jenkinson, Emma M, Forte, Gabriella MA, Anderson, Beverley H, Ariaudo, Giada, Bader-Meunier, Brigitte, Baildam, Eileen M, Battini, Roberta, Beresford, Michael W, Casarano, Manuela, Chouchane, Mondher, Cimaz, Rolando, Collins, Abigail E, Cordeiro, Nuno JV, Dale, Russell C, Davidson, Joyce E, De Waele, Liesbeth, Desguerre, Isabelle, Faivre, Laurence, Fazzi, Elisa, Isidor, Bertrand, Lagae, Lieven, Latchman, Andrew R, Lebon, Pierre, Li, Chumei, Livingston, John H, Lourenço, Charles M, Mancardi, Maria Margherita, Masurel-Paulet, Alice, McInnes, Iain B, Menezes, Manoj P, Mignot, Cyril, O’Sullivan, James, Orcesi, Simona, Picco, Paolo P, Riva, Enrica, Robinson, Robert A, Rodriguez, Diana, Salvatici, Elisabetta, Scott, Christiaan, Szybowska, Marta, Tolmie, John L, Vanderver, Adeline, Vanhulle, Catherine, Vieira, Jose Pedro, Webb, Kate, Whitney, Robyn N, Williams, Simon G, Wolfe, Lynne A, Zuberi, Sameer M, Hur, Sun, Crow, Yanick J

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