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Results 1-10 of 36 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2019
Effect of digital alteration information and disclaimer labels attached to fashion magazine advertisements on women's body dissatisfaction
Tiggemann, M.
;
Brown, Z.
;
Anderberg, I.
2019
Pathogenic abnormal splicing due to intronic deletions that induce biophysical space constraint for spliceosome assembly
Bryen, S.J.
;
Joshi, H.
;
Evesson, F.J.
;
Girard, C.
;
Ghaoui, R.
;
Waddell, L.B.
;
Testa, A.C.
;
Cummings, B.
;
Arbuckle, S.
;
Graf, N.
;
Webster, R.
;
MacArthur, D.G.
;
Laing, N.G.
;
Davis, M.R.
;
Lührmann, R.
;
Cooper, S.T.
2019
Intronic ATTTC repeat expansions in STARD7 in familial adult myoclonic epilepsy linked to chromosome 2
Corbett, M.A.
;
Kroes, T.
;
Veneziano, L.
;
Bennett, M.F.
;
Florian, R.
;
Schneider, A.L.
;
Coppola, A.
;
Licchetta, L.
;
Franceschetti, S.
;
Suppa, A.
;
Wenger, A.
;
Mei, D.
;
Pendziwiat, M.
;
Kaya, S.
;
Delledonne, M.
;
Straussberg, R.
;
Xumerle, L.
;
Regan, B.
;
Crompton, D.
;
van Rootselaar, A.-F.
;
et al.
2019
Disruptive variants of CSDE1 associate with autism and interfere with neuronal development and synaptic transmission
Guo, H.
;
Li, Y.
;
Shen, L.
;
Wang, T.
;
Jia, X.
;
Liu, L.
;
Xu, T.
;
Ou, M.
;
Hoekzema, K.
;
Wu, H.
;
Gillentine, M.A.
;
Liu, C.
;
Ni, H.
;
Peng, P.
;
Zhao, R.
;
Zhang, Y.
;
Phornphutkul, C.
;
Stegmann, A.P.A.
;
Prada, C.E.
;
Hopkin, R.J.
;
et al.
2019
Bi-allelic loss-of-function CACNA1B mutations in progressive epilepsy-dyskinesia
Gorman, K.M.
;
Meyer, E.
;
Grozeva, D.
;
Spinelli, E.
;
McTague, A.
;
Sanchis-Juan, A.
;
Carss, K.J.
;
Bryant, E.
;
Reich, A.
;
Schneider, A.L.
;
Pressler, R.M.
;
Simpson, M.A.
;
Debelle, G.D.
;
Wassmer, E.
;
Morton, J.
;
Sieciechowicz, D.
;
Jan-Kamsteeg, E.
;
Paciorkowski, A.R.
;
King, M.D.
;
Cross, J.H.
;
et al.
2019
Three pregnancies after transplantation: An 84-year-old kidney is the gift that keeps giving life
Bateman, S.M.
;
Coates, P.T.
;
Jesudason, S.
2019
Differential patterns of disease and injury in Mozambique: new perspectives from a pragmatic, multicenter, surveillance study of 7809 emergency presentations
Mocumbi, A.O.
;
Cebola, B.
;
Muloliwa, A.
;
Sebastiao, F.
;
Sitefane, S.J.
;
Manafe, N.
;
Dobe, I.
;
Lumbandali, N.
;
Keates, A.
;
Stickland, N.
;
Chan, Y.-K.
;
Stewart, S.
;
Silva, J.P.
2019
The genetic relationship between female reproductive traits and six psychiatric disorders
Ni, G.
;
Amare, A.T.
;
Zhou, X.
;
Mills, N.
;
Gratten, J.
;
Lee, S.H.
2019
Predicting seizures in pregnant women with epilepsy: development and external validation of a prognostic model
Allotey, J.
;
Fernandez-Felix, B.M.
;
Zamora, J.
;
Moss, N.
;
Bagary, M.
;
Kelso, A.
;
Khan, R.
;
van der Post, J.A.M.
;
Mol, B.W.
;
Pirie, A.M.
;
McCorry, D.
;
Khan, K.S.
;
Thangaratinam, S.
;
Chappell, L.C.
2019
Chromosomal abnormalities and prognosis in NPM1-mutated acute myeloid leukemia: a pooled analysis of individual patient data from nine international cohorts
Angenendt, L.
;
Röllig, C.
;
Montesinos, P.
;
Martínez-Cuadrón, D.
;
Barragan, E.
;
García, R.
;
Botella, C.
;
Martínez, P.
;
Ravandi, F.
;
Kadia, T.
;
Kantarjian, H.M.
;
Cortes, J.
;
Juliusson, G.
;
Lazarevic, V.
;
Höglund, M.
;
Lehmann, S.
;
Recher, C.
;
Pigneux, A.
;
Bertoli, S.
;
Dumas, P.Y.
;
et al.
Discover
Author
10
et al.
2
Avery, J.
2
Babl, F.E.
2
Beck, B.
2
Borland, M.L.
2
Braaf, S.
2
Bressan, S.
2
Cameron, P.
2
Dalton, S.
2
Furyk, J.
.
next >
Subject
12
Infant
11
Australia
6
Aged, 80 and over
6
Infant, Newborn
5
Pedigree
4
Health Services, Indigenous
4
Mutation
4
Pregnancy
4
Prognosis
4
Treatment Outcome
.
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