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Results 1-10 of 12 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
1996
Gene localisation for Wilson-Turner syndrome (WTS:MIM 309585)
Gedeon, A.
;
Turner, G.
;
Mulley, J.
1996
bcl-w, a novel member of the bcl-2 family, promotes cell survival
Gibson, L.
;
Holmgreen, S.
;
Huang, D.
;
Bernand, O.
;
Copeland, N.
;
Jenkins, N.
;
Sutherland, G.
;
Baker, E.
;
Adams, J.
;
Cory, S.
1996
A novel mutation in Exon 6 (F236S) of the proteolipid protein gene is associated with spastic paraplegia
Donnelly, A.
;
Colley, A.
;
Crimmins, D.
;
Mulley, 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.
1996
A novel X-linked gene, G4.5. is responsible for Barth Syndrome
Bione, S.
;
D'Adamo, P.
;
Maestrini, E.
;
Gedeon, A.
;
Bolhuis, P.
;
Toniolo, D.
1996
Characterization and chromosomal localization of the human A2a adenosine receptor gene - ADORA2A
Le, F.
;
Townsend-Nicholson, A.
;
Baker, E.
;
Sutherland, G.
;
Schofield, P.
1996
Molecular cloning and assignment of FAK2, a novel human focal adhesion kinase, to 8p11.2-p22 By nonisotopic in situ hybridization
Herzog, H.
;
Nicholl, J.
;
Hort, Y.
;
Sutherland, G.
;
Shine, J.
1996
Chromosomal mapping of the gene (P19) encoding the intracellular serpin proteinase inhibitor 9 to 6p25 By fluorescence in situ hybridization
Eyre, H.
;
Sun, J.
;
Sutherland, G.
;
Bird, P.
Discover
Author
6
Sutherland, G.
5
Gedeon, A.
5
Mulley, J.
3
Baker, E.
2
Nicholl, J.
2
Turner, G.
1
Adams, J.
1
Bernand, O.
1
Bione, S.
1
Bird, P.
.
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Subject
12
Humans
7
Genetic Linkage
7
X Chromosome
6
Female
5
DNA, Complementary
5
In Situ Hybridization, Fluorescence
5
Molecular Sequence Data
4
Amino Acid Sequence
4
Syndrome
3
Base Sequence
.
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