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Results 11-16 of 16 (Search time: 0.003 seconds).
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Issue Date
Title
Author(s)
2007
Molecular pathology of expanded polyalanine tract mutations in the Aristaless-related homeobox gene
Shoubridge, C.
;
Cloosterman, D.
;
Parkinson-Lawrence, E.
;
Brooks, D.
;
Gecz, J.
2003
Spondyloepiphyseal dysplasia tarda (SEDL, MIM #313400)
Savarirayan, R.
;
Thompson, E.
;
Gecz, J.
2005
Early onset seizures and Rett-like features associated with mutations in CDKL5
Evans, J.
;
Archer, H.
;
Colley, J.
;
Ravn, K.
;
Nielsen, J.
;
Kerr, A.
;
Williams, E.
;
Christodoulou, J.
;
Gecz, J.
;
Jardine, P.
;
Wright, M.
;
Pilz, D.
;
Lazarou, L.
;
Cooper, D.
;
Sampson, J.
;
Butler, R.
;
Whatley, S.
;
Clarke, A.
2007
Aristaless-related homeobox gene, the gene responsible for west syndrome and related disorders, is a groucho/transducin-like enhancer of split dependent transcriptional repressor
McKenzie, O.
;
Ponte, I.
;
Mangelsdorf, M.
;
Finnis, M.
;
Colasante, G.
;
Shoubridge, C.
;
Stifani, S.
;
Gecz, J.
;
Broccoli, V.
2014
Mutations in USP9X are associated with X-linked intellectual disability and disrupt neuronal cell migration and growth
Homan, C.
;
Kumar, R.
;
Nguyen, L.
;
Haan, E.
;
Raymond, F.
;
Abidi, F.
;
Raynaud, M.
;
Schwartz, C.
;
Wood, S.
;
Gecz, J.
;
Jolly, L.
2006
ARX: a gene for all seasons
Gecz, J.
;
Cloosterman, D.
;
Partington, M.
Discover
Author
4
Shoubridge, C.
3
Mangelsdorf, M.
3
Partington, M.
2
Broccoli, V.
2
Cloosterman, D.
2
Finnis, M.
2
Jolly, L.
2
Kalscheuer, V.
2
Schwartz, C.
2
Shaw, M.
.
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Subject
16
Humans
10
Homeodomain Proteins
9
Male
8
Animals
7
Female
5
Adult
5
Chromosomes, Human, X
5
Intellectual Disability
5
Mental Retardation, X-Linked
5
Mice
.
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Date issued
3
2010 - 2014
13
2001 - 2009