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Results 11-20 of 25 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1995
X linked fatal infantile cardiomyopathy maps to Xq28 and is possibly allelic to Barth syndrome
Gedeon, A.
;
Wilson, M.
;
Colley, A.
;
Sillence, D.
;
Mulley, J.
1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Colley, A.
;
Jamieson, R.
;
Thompson, E.
;
Rogers, J.
;
Sillence, D.
;
Tiller, G.
;
Mulley, J.
;
Gecz, J.
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.
1998
Deafness due to Pro250Arg mutation of FGFR3
Hollway, G.
;
Suthers, G.
;
Battese, K.
;
Turner, A.
;
David, D.
;
Mulley, J.
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.
1996
Identification of the gene FMR2, associated with FRAXE mental retardation
Gecz, J.
;
Gedeon, A.
;
Sutherland, G.
;
Mulley, J.
1998
Polymorphic variants within the homeobox gene MSX1: a candidate gene for developmental disorders.
Hollway, G.
;
Mulley, J.
Discover
Author
10
Gedeon, A.
8
Sutherland, G.
7
Donnelly, A.
6
Gecz, J.
4
Colley, A.
4
Phillips, H.
3
Baker, E.
3
Berkovic, S.
3
Haan, E.
3
Hollway, G.
.
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Subject
21
Humans
15
Male
14
Female
13
X Chromosome
11
Genetic Linkage
10
Intellectual Disability
10
Pedigree
9
Chromosome Mapping
8
Molecular Sequence Data
6
Genetic Markers
.
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Date issued
3
1999
7
1998
2
1997
10
1996
3
1995