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Results 41-42 of 42 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2013
Loss of Usp9x disrupts cortical architecture, hippocampal development and TGFβ-mediated axonogenesis
Stegeman, S.
;
Jolly, L.
;
Premarathne, S.
;
Gecz, J.
;
Richards, L.
;
Mackay-Sim, A.
;
Wood, S.
;
Alsina, B.
2010
A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32
Hattersley, K.
;
Laurie, K.
;
Liebelt, J.
;
Gecz, J.
;
Durkin, S.
;
Craig, J.
;
Burden, K.
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Author
8
Corbett, M.
8
et al.
8
Jolly, L.
7
Haan, E.
6
Berkovic, S.
6
Gardner, A.
6
Hackett, A.
6
Nguyen, L.
5
Scheffer, I.
4
Dibbens, L.
.
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Subject
40
Humans
38
Female
23
Mutation
18
Intellectual Disability
15
Animals
14
Pedigree
13
Child
12
Phenotype
11
Mice
9
Adult
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Date issued
6
2018
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5
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2010