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Results 61-64 of 64 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1998
PAK3 mutation in nonsyndromic X-linked mental retardation
Allen, K.
;
Gleeson, J.
;
Bagrodia, S.
;
Partington, M.
;
MacMillan, J.
;
Cerione, R.
;
Mulley, J.
;
Walsh, C.
2018
Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder
Frints, S.G.M.
;
Ozanturk, A.
;
Rodríguez Criado, G.
;
Grasshoff, U.
;
de Hoon, B.
;
Field, M.
;
Manouvrier-Hanu, S.
;
E Hickey, S.
;
Kammoun, M.
;
Gripp, K.W.
;
Bauer, C.
;
Schroeder, C.
;
Toutain, A.
;
Mihalic Mosher, T.
;
Kelly, B.J.
;
White, P.
;
Dufke, A.
;
Rentmeester, E.
;
Moon, S.
;
Koboldt, D.C.
;
et al.
2015
Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome
Walz, K.
;
Cohen, D.
;
Neilsen, P.
;
Foster, J.
;
Brancati, F.
;
Demir, K.
;
Fisher, R.
;
Moffat, M.
;
Verbeek, N.
;
Bjørgo, K.
;
Lo Castro, A.
;
Curatolo, P.
;
Novelli, G.
;
Abad, C.
;
Lei, C.
;
Zhang, L.
;
Diaz-Horta, O.
;
Young, J.
;
Callen, D.
;
Tekin, M.
2017
A mutation in the viral sensor 2’-5’-oligoadenylate synthetase 2 causes failure of lactation
Oakes, S.R.
;
Gallego-Ortega, D.
;
Stanford, P.M.
;
Junankar, S.
;
Au, W.W.Y.
;
Kikhtyak, Z.
;
von Korff, A.
;
Sergio, C.M.
;
Law, A.M.K.
;
Castillo, L.E.
;
Allerdice, S.L.
;
Young, A.I.J.
;
Piggin, C.
;
Whittle, B.
;
Bertram, E.
;
Naylor, M.J.
;
Roden, D.L.
;
Donovan, J.
;
Korennykh, A.
;
Goodnow, C.C.
;
et al.
;
Wells, C.A.
Discover
Author
17
Gecz, J.
11
et al.
8
Paton, J.
7
Ogunniyi, A.
5
Corbett, M.
5
Gardner, A.
5
Shaw, M.
5
Shoubridge, C.
5
Thomas, P.
4
Hughes, J.
.
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Subject
64
Animals
30
Female
28
Male
22
Molecular Sequence Data
17
Amino Acid Sequence
15
Pedigree
14
Intellectual Disability
13
Cell Line
12
Base Sequence
11
Brain
.
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Date issued
1
2020 - 2021
36
2010 - 2019
25
2000 - 2009
2
1997 - 1999