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Results 1-10 of 31 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2012
Paternal education status significantly influences infants’ measles vaccination uptake, independent of maternal education status
Rammohan, A.
;
Awofeso, N.
;
Fernandez, R.
2014
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.
;
Ă•unap, K.
;
Carroll, R.
;
Moeschler, J.
;
Field, M.
;
Schwartz, C.
;
Gecz, J.
;
Shi, Y.
2010
Immunogenicity of a monovalent 2009 influenza A(H1N1) vaccine in infants and children: A randomized trial
Nolan, T.
;
McVernon, J.
;
Skeljo, M.
;
Richmond, P.
;
Wadia, U.
;
Lambert, S.
;
Nissen, M.
;
Marshall, H.
;
Booy, R.
;
Heron, L.
;
Hartel, G.
;
Lai, M.
;
Basser, R.
;
Gittleson, C.
;
Greenberg, M.
2013
Gain-of-function mutations in RIT1 cause Noonan syndrome, a RAS/MAPK pathway syndrome
Aoki, Y.
;
Niihori, T.
;
Banjo, T.
;
Okamoto, N.
;
Mizuno, S.
;
Kurosawa, K.
;
Ogata, T.
;
Takada, F.
;
Yano, M.
;
Ando, T.
;
Hoshika, T.
;
Barnett, C.
;
Ohashi, H.
;
Kawame, H.
;
Hasegawa, T.
;
Okutani, T.
;
Nagashima, T.
;
Hasegawa, S.
;
Funayama, R.
;
Nagashima, T.
;
et al.
2013
Efficacy and safety of once-daily esomeprazole for the treatment of gastroesophageal reflux disease in neonatal patients
Davidson, G.
;
Wenzl, T.
;
Thomson, M.
;
Omari, T.
;
Barker, P.
;
Lundborg, P.
;
Illueca, M.
2013
Comparison of stool microbiota compositions, stool alpha1-antitrypsin and calprotectin concentrations, and diarrhoeal morbidity of Indonesian infants fed breast milk or probiotic/prebiotic-supplemented formula
Oswari, H.
;
Prayitno, L.
;
Dwipoerwantoro, P.
;
Firmansyah, A.
;
Makrides, M.
;
Lawley, B.
;
Kuhn-Sherlock, B.
;
Cleghorn, G.
;
Tannock, G.
2014
The safety of seasonal influenza vaccines in Australian children in 2013
Wood, N.
;
Blyth, C.
;
Willis, G.
;
Richmond, P.
;
Gold, M.
;
Buttery, J.
;
Crawford, N.
;
Crampton, M.
;
Yin, J.
;
Chow, M.
;
Macartney, K.
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
Interchromosomal insertional translocation at Xq26.3 alters SOX3 expression in an individual with XX male sex reversal
Haines, B.
;
Hughes, J.
;
Corbett, M.
;
Shaw, M.
;
Innes, J.
;
Patel, L.
;
Gecz, J.
;
Clayton-Smith, J.
;
Thomas, P.
Discover
Author
5
Anderson, P.J.
4
Gold, M.
4
Makrides, M.
4
Marshall, H.
3
Corbett, M.
3
Doyle, L.W.
3
et al.
3
Gecz, J.
3
Gibson, R.
3
Lee, K.J.
.
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Subject
31
Humans
27
Female
17
Child, Preschool
16
Infant, Newborn
11
Child
7
Adolescent
5
Adult
5
Australia
5
Infant, Premature
5
Mutation
.
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Date issued
3
2017
2
2016
3
2015
2
2014
6
2013
5
2012
2
2011
8
2010