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PreviewIssue DateTitleAuthor(s)
2009Induction of labour versus expectant monitoring for gestational hypertension or mild pre-eclampsia after 36 weeks' gestation (HYPITAT): a multicentre, open-label randomised controlled trialKoopmans, C.; Bijlenga, D.; Groen, H.; Vijgen, S.; Aarnoudse, J.; Bekedam, D.; van den Berg, P.; de Boer, K.; Burggraaff, J.; Bloemenkamp, K.; Drogtrop, A.; Franx, A.; de Groot, C.; Huisjes, A.; Kwee, A.; van Loon, A.; Lub, A.; Papatsonis, D.; van der Post, J.; Roumen, F.; et al.
2009Analysis of families with Lynch syndrome complicated by advanced serrated neoplasia: the importance of pathology review and pedigree analysisWalsh, M.; Buchanan, D.; Walters, R.; Roberts, A.; Arnold, S.; McKeone, D.; Clendenning, M.; Ruszkiewicz, A.; Jenkins, M.; Hopper, J.; Goldblatt, J.; George, J.; Suthers, G.; Phillips, K.; Young, G.; Macrae, F.; Drini, M.; Woods, M.; Parry, S.; Jass, J.; et al.
2009A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardationTarpey, P.; Smith, R.; Pleasance, E.; Whibley, A.; Edkins, S.; Hardy, C.; O'Meara, S.; Latimer, C.; Dicks, E.; Menzies, A.; Stephens, P.; Blow, M.; Greenman, C.; Xue, Y.; Tyler-Smith, C.; Thompson, D.; Gray, K.; Andrews, J.; Barthorpe, S.; Buck, G.; et al.
2009Structural variation in Xq28: MECP2 duplications in 1% of patients with unexplained XLMR and in 2% of male patients with severe encephalopathyLugtenberg, D.; Kleefstra, T.; Oudakker, A.; Nillesen, W.; Yntema, H.; Tzschach, A.; Raynaud, M.; Rating, D.; Journel, H.; Chelly, J.; Goizet, C.; Lacombe, D.; Pedespan, J.; Echenne, B.; Tariverdian, G.; O'Rourke, D.; King, M.; Green, A.; Van Kogelenberg, M.; Van Esch, H.; et al.
2009SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosisMarini, C.; Scheffer, I.; Nabbout, R.; Mei, D.; Cox, K.; Dibbens, L.; McMahon, J.; Iona, X.; Carpintero, R.; Elia, M.; Cilio, M.; Specchio, N.; Giordano, L.; Striano, P.; Genarro, E.; Cross, J.; Kivity, S.; Neufeld, M.; Afawi, Z.; Andermann, E.; et al.

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