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Issue Date
Title
Author(s)
2014
Pharmacological management of low milk supply with domperidone: separating fact from fiction
Grzeskowiak, L.E.
;
Amir, L.H.
2013
Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy
Braunlin, E.
;
Rosenfeld, H.
;
Kampmann, C.
;
Johnson, J.
;
Beck, M.
;
Giugliani, R.
;
Guffon, N.
;
Ketteridge, D.
;
Miranda, C.
;
Scarpa, M.
;
Schwartz, I.
;
Teles, E.
;
Wraith, J.
;
Barrios, P.
;
Dias da Silva, E.
;
Kurio, G.
;
Richardson, M.
;
Gildengorin, G.
;
Hopwood, J.
;
Imperiale, M.
;
et al.
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.
2012
BRIDGE Study warrants critique
Allen, D.
;
Parry, P.
;
Purssey, R.
;
Spielmans, G.
;
Jureidini, J.
;
Rosenlicht, N.
;
Healy, D.
;
Feinberg, I.
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.
2012
KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathy
Weckhuysen, S.
;
Mandelstam, S.
;
Suls, A.
;
Audenaert, D.
;
Deconinck, T.
;
Claes, L.
;
Deprez, L.
;
Smets, K.
;
Hristova, D.
;
Yordanova, I.
;
Jordanova, A.
;
Ceulemans, B.
;
Jansen, A.
;
Hasaerts, D.
;
Roelens, F.
;
Lagae, L.
;
Yendle, S.
;
Stanley, T.
;
Heron, S.
;
Mulley, J.
;
et al.
2012
A noncoding, regulatory mutation implicates HCFC1 in nonsyndromic intellectual disability
Huang, L.
;
Jolly, L.
;
Willis-Owen, S.
;
Gardner, A.
;
Sharma, R.
;
Douglas, E.
;
Shoubridge, C.
;
Wieczorek, D.
;
Tzschach, A.
;
Cohen, M.
;
Hackett, A.
;
Field, M.
;
Froyen, G.
;
Hu, H.
;
Haas, S.
;
Ropers, H.
;
Kalscheuer, V.
;
Corbett, M.
;
Gecz, J.
2013
Parental and societal support for adolescent immunization through school based immunization programs
Marshall, H.
;
Collins, J.
;
Sullivan, T.
;
Tooher, R.
;
O'Keefe, M.
;
Skinner, S.
;
Watson, M.
;
Burgess, T.
;
Ashmeade, H.
;
Braunack-Mayer, A.
2010
The paradox of 20q11.21 amplification in a subset of cases of myeloid malignancy with chromosome 20 deletion
MacKinnon, R.
;
Selan, C.
;
Wall, M.
;
Baker, E.
;
Nandurkar, H.
;
Campbell, L.
2016
X-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genes
Hu, H.
;
Haas, S.
;
Chelly, J.
;
Van Esch, H.
;
Raynaud, M.
;
De Brouwer, A.
;
Weinert, S.
;
Froyen, G.
;
Frints, S.
;
Laumonnier, F.
;
Zemojtel, T.
;
Love, M.
;
Richard, H.
;
Emde, A.
;
Bienek, M.
;
Jensen, C.
;
Hambrock, M.
;
Fischer, U.
;
Langnick, C.
;
Feldkamp, M.
;
et al.
Discover
Author
23
et al.
22
Gecz, J.
21
Anderson, P.J.
18
Doyle, L.W.
13
Cheong, J.L.Y.
13
Lee, K.J.
12
Makrides, M.
9
Haan, E.
9
Thompson, D.K.
8
Burnett, A.C.
.
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Subject
144
Female
65
Child
48
Child, Preschool
44
Adult
42
Adolescent
40
Infant, Newborn
39
Infant
29
Animals
29
Mutation
25
Australia
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Date issued
5
2019
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12
2016
13
2015
18
2014
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2013
26
2012
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2011
34
2010
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