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PreviewIssue DateTitleAuthor(s)
2016TBC1D24 genotype-phenotype correlationBalestrini, S.; Milh, M.; Castiglioni, C.; Lüthy, K.; Finelli, M.; Verstreken, P.; Cardon, A.; Stražišar, B.; Holder, J.; Lesca, G.; Mancardi, M.; Poulat, A.; Repetto, G.; Banka, S.; Bilo, L.; Birkeland, L.; Bosch, F.; Brockmann, K.; Cross, J.; Doummar, D.; et al.
2016Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trialBest, K.P.; Sullivan, T.; Palmer, D.; Gold, M.; Kennedy, D.J.; Martin, J.; Makrides, M.
2016Psychometric properties of translation of the Child Perception Questionnaire (CPQ11-14) in Telugu speaking Indian childrenKumar, S.; Kroon, J.; Lalloo, R.; Johnson, N.; Arakeri, G.
2016HUWE1 mutations in Juberg-Marsidi and Brooks syndromes: the results of an X-chromosome exome sequencing studyFriez, M.; Brooks, S.; Stevenson, R.; Field, M.; Basehore, M.; Adès, L.; Sebold, C.; Mcgee, S.; Saxon, S.; Skinner, C.; Craig, M.; Murray, L.; Simensen, R.; Yap, Y.; Shaw, M.; Gardner, A.; Corbett, M.; Kumar, R.; Bosshard, M.; Van Loon, B.; et al.
2016Food advertising, children's food choices and obesity: interplay of cognitive defences and product evaluation: an experimental studyTarabashkina, L.; Quester, P.; Crouch, R.
2016The psycho-social impact of malocclusions and treatment expectations of adolescent orthodontic patientsTwigge, E.; Roberts, R.; Jamieson, L.; Dreyer, C.; Sampson, W.
2016The Active For Life Year 5 (AFLY5) school-based cluster randomised controlled trial: effect on potential mediatorsLawlor, D.; Howe, L.; Anderson, E.; Kipping, R.; Campbell, R.; Wells, S.; Chittleborough, C.; Peters, T.; Jago, R.
2016Neonatal brain abnormalities associated with autism spectrum disorder in children born very pretermUre, A.M.; Treyvaud, K.; Thompson, D.K.; Pascoe, L.; Roberts, G.; Lee, K.J.; Seal, M.L.; Northam, E.; Cheong, J.L.; Hunt, R.W.; Inder, T.; Doyle, L.W.; Anderson, P.J.
2016Hypertensive disorders of pregnancy, respiratory outcomes and atopy in childhoodShaheen, S.; Macdonald-Wallis, C.; Lawlor, D.; Henderson, A.
2016Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDvan Bon, B.W.M.; Coe, B.P.; Bernier, R.; Green, C.; Gerdts, J.; Witherspoon, K.; Kleefstra, T.; Willemsen, M.H.; Kumar, R.; Bosco, P.; Fichera, M.; Li, D.; Amaral, D.; Cristofoli, F.; Peeters, H.; Haan, E.; Romano, C.; Mefford, H.C.; Scheffer, I.; Gecz, J.; et al.