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Results 21-30 of 49 (Search time: 0.005 seconds).
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Issue Date
Title
Author(s)
2019
DNA hypermethylation encroachment at CpG island borders in cancer is predisposed by H3K4 monomethylation patterns
Skvortsova, K.
;
Masle-Farquhar, E.
;
Luu, P.L.
;
Song, J.Z.
;
Qu, W.
;
Zotenko, E.
;
Gould, C.M.
;
Du, Q.
;
Peters, T.J.
;
Colino-Sanguino, Y.
;
Pidsley, R.
;
Nair, S.S.
;
Khoury, A.
;
Smith, G.C.
;
Miosge, L.A.
;
Reed, J.H.
;
Kench, J.G.
;
Rubin, M.A.
;
Horvath, L.
;
Bogdanovic, O.
;
et al.
1996
Gene localisation for Sutherland-Haan syndrome (SHS:MIM 309470)
Gedeon, A.
;
Haan, E.
;
Mulley, J.
1996
Refinement of the background genetic map of Xq26-q27 and gene localisation for Borjeson-Forssman-Lehmann syndrome
Gedeon, A.
;
Kozman, H.
;
Robinson, H.
;
Pilia, G.
;
Schlessinger, D.
;
Turner, G.
;
Mulley, J.
1996
Genetic localisation of MRX27 to Xq24-26 defines another discrete gene for non-specific X-linked mental retardation
Gedeon, A.
;
Glass, I.
;
Connor, J.
;
Mulley, J.
1999
Fibroblast growth factor homologous factor 2 (FHF2): gene structure, expression and mapping to the Börjeson-Forssman-Lehmann syndrome region in Xq26 delineated by a duplication breakpoint in a BFLS-like patient
Gecz, J.
;
Baker, E.
;
Donnelly, A.
;
Ming, J.
;
McDonald-McGinn, D.
;
Spinner, N.
;
Zackai, E.
;
Sutherland, G.
;
Mulley, J.
1999
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHM
Friend, K.
;
Crimmins, D.
;
Phan, T.
;
Sue, C.
;
Colley, A.
;
Fung, V.
;
Morris, J.
;
Sutherland, G.
;
Richards, R.
2011
Double-stranded RNA is pathogenic in Drosophila models of expanded repeat neurodegenerative diseases
Lawlor, K.
;
O'Keefe, L.
;
Samaraweera, S.
;
van Eyk, C.
;
McLeod, C.
;
Maloney, C.
;
Dang, T.
;
Suter, C.
;
Richards, R.
1998
Gene localisation for an autosomal dominant familial periodic fever to 12p13.
Mulley, J.
;
Saar, K.
;
Hewitt, G.
;
Rueschendorf, F.
;
Phillips, H.
;
Colley, A.
;
Sillence, D.
;
Reis, A.
;
Wilson, M.
2013
Contribution of copy number variants involving nonsense-mediated mRNA decay pathway genes to neuro-developmental disorders
Nguyen, L.
;
Kim, H.
;
Rosenfeld, J.
;
Shen, Y.
;
Gusella, J.
;
Lacassie, Y.
;
Layman, L.
;
Shaffer, L.
;
Gecz, J.
1997
Genetics heterogeneity in familial acute myelogenous leukemia: Evidence for a second locus at chromosome 16q21-23.2
Horwitz, M.
;
Benson, K.
;
Li, F.Q.
;
Wolff, J.
;
Leppert, M.
;
Hobson, L.
;
Mangelsdorf, M.
;
Yu, S.
;
Hewett, D.
;
Richards, R.
;
Raskind, W.
Discover
Author
16
Mulley, J.
9
Gedeon, A.
7
Callen, D.
7
et al.
7
Gecz, J.
6
Eyre, H.
6
Sutherland, G.
5
Colley, A.
5
Haan, E.
5
Richards, R.
.
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Subject
41
Female
17
Chromosome Mapping
17
Pedigree
12
Genetic Linkage
12
Intellectual Disability
12
Molecular Sequence Data
12
X Chromosome
9
Amino Acid Sequence
9
Animals
9
Genetic Markers
.
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2020 - 2022
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2010 - 2019
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2000 - 2009
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1995 - 1999