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Results 51-54 of 54 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2018
A systematic review and meta-analysis of 271 PCDH19-variant individuals identifies psychiatric comorbidities, and association of seizure onset and disease severity
Kolc, K.
;
Sadleir, L.
;
Scheffer, I.
;
Ivancevic, A.
;
Roberts, R.
;
Pham, D.
;
Gecz, J.
2017
Protocadherin 19 (PCDH19) interacts with paraspeckle protein NONO to co-regulate gene expression with estrogen receptor alpha (ERĪ±)
Pham, D.
;
Tan, C.
;
Homan, C.
;
Kolc, K.L.
;
Corbett, M.
;
McAninch, D.
;
Fox, A.
;
Thomas, P.
;
Kumar, R.
;
Gecz, J.
2011
"Blinders, phenotype, and fashionable genetic analysis": setting the record straight for epilepsy!
Mulley, J.C.
;
Heron, S.E.
;
Wallace, R.H.
;
Gecz, J.
;
Dibbens, L.M.
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
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Corbett, M.
10
Jolly, L.
9
Haan, E.
8
et al.
7
Berkovic, S.
7
Nguyen, L.
7
Scheffer, I.
7
Shoubridge, C.
6
Gardner, A.
6
Hackett, A.
.
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25
Mutation
21
Intellectual Disability
19
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17
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16
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15
Mice
14
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11
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