P02.92: Routine fetal anomaly screening: a DGH experience von Huda, S. S., Dobbie, H. G.

Volltext

Amniotic fluid phospholipid profile in multiple pregnancy and the effect of zygosity von DOBBIE, H. G., WHITTLE, M. J., WILSON, A. I., WHITFIELD, C. R.

Volltext

Phosphatidylglycerol and neonatal mortality and morbidity von Whittle, M. J., MacGillivray, Anne I., Hanretty, K. P., Dobbie, H. G., Howie, Catherine A.

Volltext

Exploring the association between school-based peer networks and smoking according to socioeconomic status and tobacco control context: a systematic review von Littlecott, H J, Moore, G F, McCann, M, Melendez-Torres, G J, Mercken, L, Reed, H, Mann, M, Dobbie, F, Hawkins, J

Volltext

Perceptions of friendship, peers and influence on adolescent smoking according to tobacco control context: a systematic review and meta-ethnography of qualitative research von Littlecott, H J, Moore, G F, Evans, R E, Melendez-Torres, G J, McCann, M, Reed, H, Mann, M, Dobbie, F, Jennings, S, Donaldson, C, Hawkins, J

Volltext

Associations between school-based peer networks and smoking according to socioeconomic status and tobacco control context: protocol for a mixed method systematic review von Littlecott, H J, Hawkins, J, Mann, M, Melendez-Torres, G J, Dobbie, F, Moore, G

Volltext

Mutations in different components of FGF signaling in LADD syndrome von Wollnik, Bernd, Rohmann, Edyta, Brunner, Han G, Kayserili, Hülya, Uyguner, Oya, Nürnberg, Gudrun, Lew, Erin D, Dobbie, Angus, Eswarakumar, Veraragavan P, Uzumcu, Abdullah, Ulubil-Emeroglu, Melike, Leroy, Jules G, Li, Yun, Becker, Christian, Lehnerdt, Kai, Cremers, Cor W R J, Yüksel-Apak, Memnune, Nürnberg, Peter, Kubisch, Christian, Schlessinger, Joseph, van Bokhoven, Hans

Volltext

Fifteen new T dwarfs discovered in the UKIDSS Large Area Survey von Pinfield, D. J., Burningham, B., Tamura, M., Leggett, S. K., Lodieu, N., Lucas, P. W., Mortlock, D. J., Warren, S. J., Homeier, D., Ishii, M., Deacon, N. R., McMahon, R. G., Hewett, P. C., Osori, M. R. Zapatero, Martin, E. L., Jones, H. R. A., Venemans, B. P., Day-Jones, A. C., Dobbie, P. D., Folkes, S. L., Dye, S., Allard, F., Baraffe, I., Barrado y Navascués, D., Casewell, S. L., Chiu, K., Chabrier, G., Clarke, F., Hodgkin, S. T., Magazzù, A., McCaughrean, M. J., Nakajima, T., Pavlenko, Y., Tinney, C. G.

Volltext

Rapid Actin Transport during Cell Protrusion von Zicha, Daniel, Dobbie, Ian M., Holt, Mark R., Monypenny, James, Daniel Y. H. Soong, Gray, Colin, Dunn, Graham A.

Volltext

Genome-wide ENU mutagenesis in combination with high density SNP analysis and exome sequencing provides rapid identification of novel mouse models of developmental disease von Caruana, Georgina, Farlie, Peter G, Hart, Adam H, Bagheri-Fam, Stefan, Wallace, Megan J, Dobbie, Michael S, Gordon, Christopher T, Miller, Kerry A, Whittle, Belinda, Abud, Helen E, Arkell, Ruth M, Cole, Timothy J, Harley, Vincent R, Smyth, Ian M, Bertram, John F

Volltext

CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language von Snijders Blok, Lot, Rousseau, Justine, Twist, Joanna, Ehresmann, Sophie, Takaku, Motoki, Venselaar, Hanka, Rodan, Lance H., Nowak, Catherine B., Douglas, Jessica, Swoboda, Kathryn J., Steeves, Marcie A., Sahai, Inderneel, Stumpel, Connie T. R. M., Stegmann, Alexander P. A., Wheeler, Patricia, Willing, Marcia, Fiala, Elise, Kochhar, Aaina, Gibson, William T., Cohen, Ana S. A., Agbahovbe, Ruky, Innes, A. Micheil, Au, P. Y. Billie, Rankin, Julia, Anderson, Ilse J., Skinner, Steven A., Louie, Raymond J., Warren, Hannah E., Afenjar, Alexandra, Keren, Boris, Nava, Caroline, Buratti, Julien, Isapof, Arnaud, Rodriguez, Diana, Lewandowski, Raymond, Propst, Jennifer, van Essen, Ton, Choi, Murim, Lee, Sangmoon, Chae, Jong H., Price, Susan, Schnur, Rhonda E., Douglas, Ganka, Wentzensen, Ingrid M., Zweier, Christiane, Reis, André, Bialer, Martin G., Moore, Christine, Koopmans, Marije, Brilstra, Eva H., Monroe, Glen R., van Gassen, Koen L. I., van Binsbergen, Ellen, Newbury-Ecob, Ruth, Bownass, Lucy, Bader, Ingrid, Mayr, Johannes A., Wortmann, Saskia B., Jakielski, Kathy J., Strand, Edythe A., Kloth, Katja, Bierhals, Tatjana, Roberts, John D., Petrovich, Robert M., Machida, Shinichi, Kurumizaka, Hitoshi, Lelieveld, Stefan, Pfundt, Rolph, Jansen, Sandra, Deriziotis, Pelagia, Faivre, Laurence, Thevenon, Julien, Assoum, Mirna, Shriberg, Lawrence, Kleefstra, Tjitske, Brunner, Han G., Wade, Paul A., Fisher, Simon E., Campeau, Philippe M.

Volltext

Equitable Expanded Carrier Screening Needs Indigenous Clinical and Population Genomic Data von Easteal, Simon, Arkell, Ruth M., Balboa, Renzo F., Bellingham, Shayne A., Brown, Alex D., Calma, Tom, Cook, Matthew C., Davis, Megan, Dawkins, Hugh J.S., Dinger, Marcel E., Dobbie, Michael S., Farlow, Ashley, Gwynne, Kylie G., Hermes, Azure, Hoy, Wendy E., Jenkins, Misty R., Jiang, Simon H., Kaplan, Warren, Leslie, Stephen, Llamas, Bastien, Mann, Graham J., McMorran, Brendan J., McWhirter, Rebekah E., Meldrum, Cliff J., Nagaraj, Shivashankar H., Newman, Saul J., Nunn, Jack S., Ormond-Parker, Lyndon, Orr, Neil J., Paliwal, Devashi, Patel, Hardip R., Pearson, Glenn, Pratt, Greg R., Rambaldini, Boe, Russell, Lynette W., Savarirayan, Ravi, Silcocks, Matthew, Skinner, John C., Souilmi, Yassine, Vinuesa, Carola G., Baynam, Gareth

Volltext

Loss of Atrx affects trophoblast development and the pattern of X-inactivation in extraembryonic tissues von Garrick, David, Sharpe, Jackie A, Arkell, Ruth, Dobbie, Lorraine, Smith, Andrew J H, Wood, William G, Higgs, Douglas R, Gibbons, Richard J

Volltext

Collaboration Recommendation on Academic Social Networks von Lopes, Giseli Rabello, Moro, Mirella M., Wives, Leandro Krug, de Oliveira, José Palazzo Moreira

Volltext

Mutations in the PP2A regulatory subunit B family genes PPP2R5B, PPP2R5C and PPP2R5D cause human overgrowth von Loveday, Chey, Tatton-Brown, Katrina, Clarke, Matthew, Westwood, Isaac, Renwick, Anthony, Ramsay, Emma, Nemeth, Andrea, Campbell, Jennifer, Joss, Shelagh, Gardner, McKinlay, Zachariou, Anna, Elliott, Anna, Ruark, Elise, van Montfort, Rob, Rahman, Nazneen

Volltext

Eight new T4.5–T7.5 dwarfs discovered in the UKIDSS Large Area Survey Data Release 1 von Lodieu, N., Pinfield, D. J., Leggett, S. K., Jameson, R. F., Mortlock, D. J., Warren, S. J., Burningham, B., Lucas, P. W., Chiu, K., Liu, M. C., Venemans, B. P., McMahon, R. G., Allard, F., Baraffe, I., Y Navascués, D. Barrado, Carraro, G., Casewell, S. L., Chabrier, G., Chappelle, R. J., Clarke, F., Day-Jones, A. C., Deacon, N. R., Dobbie, P. D., Folkes, S. L., Hambly, N. C., Hewett, P. C., Hodgkin, S. T., Jones, H. R. A., Kendall, T. R., Magazzù, A., Martín, E. L., McCaughrean, M. J., Nakajima, T., Pavlenko, Y., Tamura, M., Tinney, C. G., Zapatero Osorio, M. R.

Volltext

Functional traits shed new light on the nature of ecotones: a study across a bog-to-forest sequence von Brownstein, G, T. F. Döbert, L. R. Dobbie, N. H. Hashim, J. Bastow Wilson

Volltext

Deficiencies in education and experience in the management of acute kidney injury among Malawian healthcare workers von Evans, R, Rudd, P, Hemmila, U, Dobbie, H, Dreyer, G

Volltext

Genome-wide screening reveals the genetic basis of mammalian embryonic eye development von Chee, Justine M, Lanoue, Louise, Clary, Dave, Higgins, Kendall, Bower, Lynette, Flenniken, Ann, Guo, Ruolin, Adams, David J, Bosch, Fatima, Braun, Robert E, Brown, Steve D M, Chin, H-J Genie, Dickinson, Mary E, Hsu, Chih-Wei, Dobbie, Michael, Gao, Xiang, Galande, Sanjeev, Grobler, Anne, Heaney, Jason D, Herault, Yann, de Angelis, Martin Hrabe, Mammano, Fabio, Nutter, Lauryl M J, Parkinson, Helen, Qin, Chuan, Shiroishi, Toshi, Sedlacek, Radislav, Seong, J-K, Xu, Ying, Brooks, Brian, McKerlie, Colin, Lloyd, K C Kent, Westerberg, Henrik, Moshiri, Ala

Volltext

Weaver syndrome and EZH2 mutations: Clarifying the clinical phenotype von Tatton-Brown, Katrina, Murray, Anne, Hanks, Sandra, Douglas, Jenny, Armstrong, Ruth, Banka, Siddharth, Bird, Lynne M., Clericuzio, Carol L., Cormier-Daire, Valerie, Cushing, Tom, Flinter, Frances, Jacquemont, Marie-Line, Joss, Shelagh, Kinning, Esther, Lynch, Sally Ann, Magee, Alex, McConnell, Vivienne, Medeira, Ana, Ozono, Keiichi, Patton, Michael, Rankin, Julia, Shears, Debbie, Simon, Marleen, Splitt, Miranda, Strenger, Volker, Stuurman, Kyra, Taylor, Clare, Titheradge, Hannah, Van Maldergem, Lionel, Temple, I. Karen, Cole, Trevor, Seal, Sheila, Rahman, Nazneen

Volltext