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Results 1-7 of 7 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2004
Disruption of a new X linked gene highly expressed in brain in a family with two mentally retarded males
Cantagrel, V.
;
Lossi, A.
;
Boulanger, S.
;
Depetris, D.
;
Mattei, M.
;
Gecz, J.
;
Schwartz, C.
;
van Maldergem, L.
;
Villard, L.
2004
TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation
Christophe-Hobertus, C.
;
Kooy, F.
;
Gecz, J.
;
Abramowicz, M.
;
Holinski-Feder, E.
;
Schwartz, C.
;
Christophe, D.
2005
XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene
Stepp, M.
;
Cason, A.
;
Finnis, M.
;
Mangelsdorf, M.
;
Holinski-Feder, E.
;
Macgregor, D.
;
MacMillan, A.
;
Holden, J.
;
Gecz, J.
;
Stevenson, R.
;
Schwartz, C.
2006
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
Hagens, O.
;
Dubos, A.
;
Abidi, F.
;
Barbi, G.
;
Van Zutven, L.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Moraine, C.
;
Fryns, J.
;
Chelly, J.
;
van Bokhoven, H.
;
Gecz, J.
;
Dollfus, H.
;
Ropers, H.
;
Schwartz, C.
;
de Cassia Stocco dos Santos, R.
;
Kalscheuer, V.
;
Hanauer, A.
2007
Mutations in ionotropic AMPA receptor 3 alter channel properties and are associated with moderate cognitive impairment in humans
Wu, Y.
;
Arai, A.
;
Rumbaugh, G.
;
Srivastava, A.
;
Turner, G.
;
Hayashi, T.
;
Suzuki, E.
;
Jiang, Y.
;
Zhang, L.
;
Rodriguez, J.
;
Boyle, J.
;
Tarpey, P.
;
Raymond, F.
;
Nevelsteen, J.
;
Froyen, G.
;
Stratton, M.
;
Futreal, P.
;
Gecz, J.
;
Stevenson, R.
;
Schwartz, C.
;
et al.
2008
XLMR genes: update 2007
Chiurazzi, P.
;
Schwartz, C.
;
Gecz, J.
;
Neri, G.
2002
Abnormal expression of the KLF8 (ZNF741) gene in a female patient with an X;autosome translocation t(X;21)(p11.2;q22.3) and non-syndromic mental retardation
Lossi, A.
;
Laugier-Anfossi, F.
;
Depetris, D.
;
Gecz, J.
;
Gedeon, A.
;
Kooy, F.
;
Schwartz, C.
;
Mattei, M.
;
Croquette, M.
;
Villard, L.
Discover
Author
2
Depetris, D.
2
Holinski-Feder, E.
2
Kooy, F.
2
Lossi, A.
2
Mattei, M.
2
Stevenson, R.
2
Villard, L.
1
Abidi, F.
1
Abramowicz, M.
1
Arai, A.
.
next >
Subject
3
Humans
3
Mental Retardation, X-Linked
3
Mutation
2
Chromosomes, Human, X
2
Female
2
Male
1
3' Untranslated Regions
1
Amino Acid Sequence
1
Animals
1
Base Sequence
.
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Date issued
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2005
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2004
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2002