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Issue Date
Title
Author(s)
2014
SOX3 deletion in mouse and human Is associated with persistence of the craniopharyngeal canal
Alatzoglou, K.
;
Azriyanti, A.
;
Rogers, N.
;
Ryan, F.
;
Curry, N.
;
Noakes, C.
;
Bignell, P.
;
Hall, G.
;
Littooij, A.
;
Saunders, D.
;
Thomas, P.
;
Stewart, H.
;
Dattani, M.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
2012
Congenital hydrocephalus and abnormal subcommissural organ development in Sox3 transgenic mice
Lee, K.
;
Tan, J.
;
Morris, M.
;
Rizzoti, K.
;
Hughes, J.
;
Cheah, P.
;
Felquer, F.
;
Liu, X.
;
Piltz, S.
;
Lovell-Badge, R.
;
Thomas, P.
;
Schmidt, J.V.
2016
Pcdh19 loss-of-function increases neuronal migration in vitro but is dispensable for brain development in mice
Pederick, D.
;
Homan, C.
;
Jaehne, E.
;
Piltz, S.
;
Haines, B.
;
Baune, B.
;
Jolly, L.
;
Hughes, J.
;
Gecz, J.
;
Thomas, P.
2013
Mammalian sex determination and gonad development
Wilhelm, D.
;
Yang, J.
;
Thomas, P.
Discover
Author
3
Hughes, J.
2
Gecz, J.
2
Piltz, S.
1
Afawi, Z.
1
Alatzoglou, K.
1
Azriyanti, A.
1
Bassan, H.
1
Baune, B.
1
Bignell, P.
1
Cheah, P.
.
next >
Subject
5
Animals
4
Humans
3
Female
2
Brain
2
Child, Preschool
2
Genotype
2
Mice, Knockout
2
SOXB1 Transcription Factors
1
Abnormalities, Multiple
1
Age of Onset
.
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Date issued
1
2016
1
2014
1
2013
2
2012