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Results 41-50 of 54 (Search time: 0.004 seconds).
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Issue Date
Title
Author(s)
1995
FRAXE and mental retardation
Mulley, J.
;
Yu, S.
;
Loesch, D.
;
Hay, D.
;
Donnelly, A.
;
Gedeon, A.
;
Carbonell, P.
;
Lopez, I.
;
Glover, G.
;
Garbarron, I.
;
Yu, P.
;
Baker, E.
;
Haan, E.
;
Hockey, A.
;
Knight, S.
;
Daview, K.
;
Richards, R.
;
Sutherland, G.
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.
2006
A conserved supergene locus controls colour pattern diversity in Heliconius butterflies
Joron, M.
;
Papa, R.
;
Beltrán, M.
;
Chamberlain, N.
;
Mavárez, J.
;
Baxter, S.
;
Abanto, M.
;
Bermingham, E.
;
Humphray, S.J.
;
Rogers, J.
;
Beasley, H.
;
Barlow, K.
;
Ffrench-Constant, R.H.
;
Mallet, J.
;
McMillan, W.O.
;
Jiggins, C.D.
;
Noor, M.A.F.
2017
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
Stessman, H.
;
Xiong, B.
;
Coe, B.
;
Wang, T.
;
Hoekzema, K.
;
Fenckova, M.
;
Kvarnung, M.
;
Gerdts, J.
;
Trinh, S.
;
Cosemans, N.
;
Vives, L.
;
Lin, J.
;
Turner, T.
;
Santen, G.
;
Ruivenkamp, C.
;
Kriek, M.
;
Van Haeringen, A.
;
Aten, E.
;
Friend, K.
;
Liebelt, J.
;
et al.
2018
A genotype-first approach identifies an intellectual disability-overweight syndrome caused by PHIP haploinsufficiency
Jansen, S.
;
Hoischen, A.
;
Coe, B.
;
Carvill, G.
;
van Esch, H.
;
Bosch, D.
;
Andersen, U.
;
Baker, C.
;
Bauters, M.
;
Bernier, R.
;
van Bon, B.
;
Claahsen-van der Grinten, H.
;
Gecz, J.
;
Gilissen, C.
;
Grillo, L.
;
Hackett, A.
;
Kleefstra, T.
;
Koolen, D.
;
Kvarnung, M.
;
Larsen, M.
;
et al.
1998
Localisation of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.
Kremmidiotis, G.
;
Baker, E.
;
Crawford, J.
;
Eyre, H.
;
Nahmias, J.
;
Callen, D.
2017
Modelling predictors of molecular response to frontline imatinib for patients with chronic myeloid leukaemia
Banjar, H.
;
Ranasinghe, D.
;
Brown, F.
;
Adelson, D.
;
Kroger, T.
;
Leclercq, T.
;
White, D.
;
Hughes, T.
;
Chaudhri, N.
;
Speletas, M.
1999
Characterization of the human glutamate receptor subunit 3 gene (GRIA3), a candidate for bipolar disorder and nonspecific X-linked mental retardation
Gecz, J.
;
Barnett, S.
;
Liu, J.
;
Hollway, G.
;
Donnelly, A.
;
Eyre, H.
;
Eshkevari, H.
;
Baltazar, R.
;
Grunn, A.
;
Nagaraja, R.
;
Gilliam, C.
;
Peltonen, L.
;
Sutherland, G.
;
Baron, M.
;
Mulley, J.
1998
Characterisation and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer
Whitmore, S.
;
Settasatian, C.
;
Crawford, J.
;
Lower, K.
;
McCallum, B.
;
Seshadri, R.
;
Cornelisse, C.
;
Moerland, E.
;
Cleton-Jansen, A.M.
;
Tipping, A.
;
Mathew, C.
;
Savnio, M.
;
Savoia, A.
;
Verlander, P.
;
Auerbach, A.
;
Van Berkel, C.
;
Pronk, J.
;
Doggett, N.
;
Callen, D.
1998
ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, & is shown to be expressed in primitive hematopoietic precursors.
Kuss, B.
;
O'Neill, G.
;
Eyre, H.
;
Doggett, N.
;
Callen, D.
;
Davey, R.
Discover
Author
15
Mulley, J.
9
Callen, D.
8
et al.
8
Gedeon, A.
6
Eyre, H.
6
Gecz, J.
6
Sutherland, G.
5
Colley, A.
5
Crawford, J.
5
Haan, E.
.
next >
Subject
47
Humans
45
Male
16
Pedigree
14
Animals
14
Molecular Sequence Data
13
Chromosome Mapping
12
Genetic Linkage
12
Intellectual Disability
12
X Chromosome
9
Adult
.
next >
Date issued
8
2020 - 2022
16
2010 - 2019
1
2000 - 2009
29
1995 - 1999