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Results 1-10 of 15 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2015
Zinc supplementation for improving pregnancy and infant outcome
Ota, E.
;
Mori, R.
;
Middleton, P.F.
;
Tobe-Gai, R.
;
Mahomed, K.
;
Miyazaki, C.
;
Bhutta, Z.A.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
2015
Influenza vaccination during pregnancy: a systematic review of fetal death, spontaneous abortion, and congenital malformation safety outcomes
McMillan, M.
;
Porritt, K.
;
Kralik, D.
;
Costi, L.
;
Marshall, H.
2015
Brain structural and microstructural alterations associated with cerebral palsy and motor impairments in adolescents born extremely preterm and/or extremely low birthweight
Kelly, C.E.
;
Chan, L.
;
Burnett, A.C.
;
Lee, K.J.
;
Connelly, A.
;
Anderson, P.J.
;
Doyle, L.W.
;
Cheong, J.L.Y.
;
Thompson, D.K.
2015
Pharmacological management of low milk supply with domperidone: separating fact from fiction
Grzeskowiak, L.E.
;
Amir, L.H.
2015
Mutations in the intellectual disability gene KDM5C reduce protein stability and demethylase activity
Brookes, E.
;
Laurent, B.
;
Õunap, K.
;
Carroll, R.
;
Moeschler, J.
;
Field, M.
;
Schwartz, C.
;
Gecz, J.
;
Shi, Y.
2015
HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain.
Jolly, L.
;
Nguyen, L.
;
Domingo, D.
;
Sun, Y.
;
Barry, S.
;
Hancarova, M.
;
Plevova, P.
;
Vlckova, M.
;
Havlovicova, M.
;
Kalscheuer, V.
;
Graziano, C.
;
Pippucci, T.
;
Bonora, E.
;
Sedlacek, Z.
;
Gecz, J.
2015
Oocyte induction of EGF responsiveness in somatic cells is associated with the acquisition of porcine oocyte developmental competence
Ritter, L.
;
Sugimura, S.
;
Gilchrist, R.
2015
Homozygous mutation of STXBP5L explains an autosomal recessive infantile-onset neurodegenerative disorder
Kumar, R.
;
Corbett, M.
;
Smith, N.
;
Jolly, L.
;
Tan, C.
;
Keating, D.
;
Duffield, M.
;
Utsumi, T.
;
Moriya, K.
;
Smith, K.
;
Hoischen, A.
;
Abbott, K.
;
Harbord, M.
;
Compton, A.
;
Woenig, J.
;
Arts, P.
;
Kwint, M.
;
Wieskamp, N.
;
Gijsen, S.
;
Veltman, J.
;
et al.
2015
Developmental disorders: deciphering exomes on a grand scale
Gecz, J.
;
Corbett, M.
Discover
Author
4
Gecz, J.
2
Amir, L.H.
2
Anderson, P.J.
2
Cheong, J.L.Y.
2
Corbett, M.
2
Doyle, L.W.
2
et al.
2
Grzeskowiak, L.E.
2
Jolly, L.
2
Lee, K.J.
.
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Subject
13
Humans
10
Male
4
Adult
4
Animals
4
Infant, Newborn
4
Mutation
3
Adolescent
3
Child
3
Intellectual Disability
3
Pregnancy
.
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