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Results 1-10 of 19 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2016
TBC1D24 genotype-phenotype correlation
Balestrini, 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.
2016
Prenatal fish oil supplementation and allergy: 6-year follow-up of a randomized controlled trial
Best, K.P.
;
Sullivan, T.
;
Palmer, D.
;
Gold, M.
;
Kennedy, D.J.
;
Martin, J.
;
Makrides, M.
2016
Psychometric properties of translation of the Child Perception Questionnaire (CPQ11-14) in Telugu speaking Indian children
Kumar, S.
;
Kroon, J.
;
Lalloo, R.
;
Johnson, N.
;
Arakeri, G.
2016
Food advertising, children's food choices and obesity: interplay of cognitive defences and product evaluation: an experimental study
Tarabashkina, L.
;
Quester, P.
;
Crouch, R.
2016
Characterizing and predicting trajectories of disordered eating over adolescence
Fairweather-Schmidt, A.K.
;
Wade, T.D.
2016
The psycho-social impact of malocclusions and treatment expectations of adolescent orthodontic patients
Twigge, E.
;
Roberts, R.
;
Jamieson, L.
;
Dreyer, C.
;
Sampson, W.
2016
The Active For Life Year 5 (AFLY5) school-based cluster randomised controlled trial: effect on potential mediators
Lawlor, D.
;
Howe, L.
;
Anderson, E.
;
Kipping, R.
;
Campbell, R.
;
Wells, S.
;
Chittleborough, C.
;
Peters, T.
;
Jago, R.
2016
Hypertensive disorders of pregnancy, respiratory outcomes and atopy in childhood
Shaheen, S.
;
Macdonald-Wallis, C.
;
Lawlor, D.
;
Henderson, A.
2016
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID
van 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.
2016
Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders
Moey, C.
;
Hinze, S.
;
Brueton, L.
;
Morton, J.
;
McMullan, D.
;
Kamien, B.
;
Barnett, C.
;
Brunetti-Pierri, N.
;
Nicholl, J.
;
Gecz, J.
;
Shoubridge, C.
Discover
Author
4
et al.
3
Anderson, P.J.
3
Gecz, J.
2
Chittleborough, C.
2
Dreyer, C.
2
Jamieson, L.
2
Lawlor, D.
2
Makrides, M.
2
Mefford, H.C.
2
Roberts, R.
.
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Subject
19
Humans
16
Male
10
Adolescent
8
Child, Preschool
6
Adult
6
Infant
5
Pregnancy
5
Young Adult
4
Australia
4
Cohort Studies
.
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