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Results 1-10 of 47 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2000
FMR3 is a novel gene associated with FRAXE CpG island and transcriptionally silent in FRAXE full mutations
Gecz, J.
2019
Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females
Jackson, M.R.
;
Loring, K.E.
;
Homan, C.C.
;
Thai, H.N.
;
Määttänen, L.
;
Arvio, M.
;
Jarvela, I.
;
Shaw, M.
;
Gardner, A.
;
Gecz, J.
;
Shoubridge, C.
2019
A recurrent missense variant in SLC9A7 causes nonsyndromic X-linked intellectual disability with alteration of Golgi acidification and aberrant glycosylation
Khayat, W.
;
Hackett, A.
;
Shaw, M.
;
Ilie, A.
;
Dudding-Byth, T.
;
Kalscheuer, V.M.
;
Christie, L.
;
Corbett, M.A.
;
Juusola, J.
;
Friend, K.L.
;
Kirmse, B.M.
;
Gecz, J.
;
Field, M.
;
Orlowski, J.
2015
Novel IL1RAPL1 mutations associated with intellectual disability impair synaptogenesis
Ramos-Brossier, M.
;
Montani, C.
;
Lebrun, N.
;
Gritti, L.
;
Martin, C.
;
Seminatore-Nole, C.
;
Toussaint, A.
;
Moreno, S.
;
Poirier, K.
;
Dorseuil, O.
;
Chelly, J.
;
Hackett, A.
;
Gecz, J.
;
Bieth, E.
;
Faudet, A.
;
Heron, D.
;
Kooy, R.
;
Loeys, B.
;
Humeau, Y.
;
Sala, C.
;
et al.
2015
Copy number variants in patients with intellectual disability affect the regulation of ARX transcription factor gene
Ishibashi, M.
;
Manning, E.
;
Shoubridge, C.
;
Krecsmarik, M.
;
Hawkins, T.
;
Giacomotto, J.
;
Zhao, T.
;
Mueller, T.
;
Bader, P.
;
Cheung, S.
;
Stankiewicz, P.
;
Bain, N.
;
Hackett, A.
;
Reddy, C.
;
Mechaly, A.
;
Peers, B.
;
Wilson, S.
;
Lenhard, B.
;
Bally-Cuif, L.
;
Gecz, J.
;
et al.
2000
Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome
Villard, L.
;
Fontes, M.
;
Ades, L.
;
Gecz, J.
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.
2023
The ribose methylation enzyme FTSJ1 has a conserved role in neuron morphology and learning performance.
Brazane, M.
;
Dimitrova, D.G.
;
Pigeon, J.
;
Paolantoni, C.
;
Ye, T.
;
Marchand, V.
;
Da Silva, B.
;
Schaefer, E.
;
Angelova, M.T.
;
Stark, Z.
;
Delatycki, M.
;
Dudding-Byth, T.
;
Gecz, J.
;
Plaçais, P.-Y.
;
Teysset, L.
;
Préat, T.
;
Piton, A.
;
Hassan, B.A.
;
Roignant, J.-Y.
;
Motorin, Y.
;
et al.
2007
Loss of SLC38A5 and FTSJ1 at Xp11.23 in three brothers with non-syndromic mental retardation due to a microdeletion in an unstable genomic region
Froyen, G.
;
Bauters, M.
;
Boyle, J.
;
Van Esch, H.
;
van Bokhoven, H.
;
Ropers, H.
;
Moraine, C.
;
Chelly, J.
;
Fryns, J.
;
Marynen, P.
;
Gecz, J.
;
Turner, G.
2002
Variable expression of mental retardation, autism, seizures, and dystonic hand movements in two families with an identical ARX gene mutation
Turner, G.
;
Partington, M.
;
Kerr, B.
;
Mangelsdorf, M.
;
Gecz, J.
Discover
Author
8
et al.
7
Haan, E.
6
Hackett, A.
6
Jolly, L.
6
Mulley, J.
6
Nguyen, L.
6
Shaw, M.
6
Sutherland, G.
6
Turner, G.
5
Fryns, J.
.
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Subject
12
Amino Acid Sequence
11
Child
11
Mice
11
Phenotype
10
Syndrome
9
Chromosomes, Human, X
9
Infant
8
Base Sequence
8
Brain
8
Gene Expression
.
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