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PreviewIssue DateTitleAuthor(s)
2010PHF6 mutations in T-cell acute lymphoblastic leukemiaVan Vlierberghe, P.; Palomero, T.; Khiabanian, H.; Van der Meulen, J.; Castillo, M.; Van Roy, N.; De Moerloose, B.; Philippe, J.; Gonzalez-Garcia, M.; Toribio, M.; Taghon, T.; Zuurbier, L.; Cauwelier, B.; Harrison, C.; Schwab, C.; Pisecker, M.; Strehl, S.; Langerak, A.; Gecz, J.; Sonneveld, E.; et al.
2010De novo mutations of SETBP1 cause Schinzel-Giedion syndromeHoischen, A.; Van Bon, B.; Gilissen, C.; Arts, P.; van Lier, B.; Steehouwer, M.; de Vries, P.; de Reuver, R.; Wieskamp, N.; Mortier, G.; Devriendt, K.; Amorim, M.; Revencu, N.; Kidd, A.; Barbosa, M.; Turner, A.; Smith, J.; Olay, C.; Henderson, A.; Hayes, I.; et al.
2013IFPA Meeting 2012 Workshop Report II: Epigenetics and imprinting in the placenta, growth factors and villous trophoblast differentiation, role of the placenta in regulating fetal exposure to xenobiotics during pregnancy, infection and the placentaAhmed, M.; Aleksunes, L.; Boeuf, P.; Chung, M.; Daoud, G.; Desoye, G.; Diaz, P.; Golos, T.; Illsley, N.; Kikuchi, K.; Komatsu, R.; Lao, T.; Morales-Prieto, D.; Nanovskaya, T.; Nobuzane, T.; Roberts, C.; Saffery, R.; Tamura, I.; Tamura, K.; Than, N.; et al.
2011Mutations in U4atac snRNA, a component of the minor spliceosome, in the developmental disorder MOPD IHe, H.; Liyanarachchi, S.; Akagi, K.; Nagy, R.; Li, J.; Dietrich, R.; Li, W.; Sebastian, N.; Wen, B.; Xin, B.; Singh, J.; Yan, P.; Alder, H.; Haan, E.; Wieczorek, D.; Albrecht, B.; Puffenberger, E.; Wang, H.; Westman, J.; Padgett, R.; et al.
2012Repeat prenatal corticosteroid prior to preterm birth: a systematic review and individual participant data meta-analysis for the PRECISE study group (prenatal repeat corticosteroid international IPD study group: assessing the effects using the best level of evidence) - study protocolCrowther, C.; Aghajafari, F.; Askie, L.; Asztalos, E.; Brocklehurst, P.; Bubner, T.; Doyle, L.; Dutta, S.; Garite, T.; Guinn, D.; Hallman, M.; Hannah, M.; Hardy, P.; Maurel, K.; Mazumder, P.; McEvoy, C.; Middleton, P.; Murphy, K.; Peltoniemi, O.; Peters, D.; et al.
2010Lynch syndrome-associated breast cancers: Clinicopathologic characteristics of a case series from the colon cancer family registryWalsh, M.; Buchanan, D.; Cummings, M.; Pearson, S.; Arnold, S.; Clendenning, M.; Walters, R.; McKeone, D.; Spurdle, A.; Hopper, J.; Jenkins, M.; Phillips, K.; Suthers, G.; George, J.; Goldblatt, J.; Muir, A.; Tucker, K.; Pelzer, E.; Gattas, M.; Woodall, S.; et al.
2017Docosahexaenoic acid and bronchopulmonary dysplasia in preterm infantsCollins, C.; Makrides, M.; McPhee, A.; Sullivan, T.; Davis, P.; Thio, M.; Simmer, K.; Rajadurai, V.; Travadi, J.; Berry, M.; Liley, H.; Opie, G.; Tan, K.; Lui, K.; Morris, S.; Stack, J.; Stark, M.; Chua, M.; Jayagobi, P.; Holberton, J.; et al.
2010Cardiotocography plus ST analysis of fetal electrocardiogram compared with cardiotocography only for intrapartum monitoring: a randomized controlled trialWesterhuis, M.; Visser, G.; Moons, K.; van Beek, E.; Benders, M.; Bijvoet, S.; van Dessel, H.; Drogtrop, A.; van Geijn, H.; Graziosi, G.; Groenendaal, F.; van Lith, J.; Nijhuis, J.; Oei, S.; Oosterbaan, H.; Porath, M.; Rijnders, R.; Schuitemaker, N.; Sopacua, L.; van der Tweel, I.; et al.
2018Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorderFrints, S.G.M.; Ozanturk, A.; Rodríguez Criado, G.; Grasshoff, U.; de Hoon, B.; Field, M.; Manouvrier-Hanu, S.; E Hickey, S.; Kammoun, M.; Gripp, K.W.; Bauer, C.; Schroeder, C.; Toutain, A.; Mihalic Mosher, T.; Kelly, B.J.; White, P.; Dufke, A.; Rentmeester, E.; Moon, S.; Koboldt, D.C.; et al.
2013Effect of maintenance tocolysis with nifedipine in threatened preterm labor on perinatal outcomes: a randomized controlled trialRoos, C.; Spaanderman, M.; Schuit, E.; Bloemenkamp, K.; Bolte, A.; Cornette, J.; Duvekot, J.; van Eyck, J.; Franssen, M.; de Groot, C.; Kok, J.; Kwee, A.; Merien, A.; Bijivank, B.; Opmeer, B.; Oudijk, M.; van Pampus, M.; Papatsonis, D.; Porath, M.; Scheepers, H.; et al.