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Issue Date
Title
Author(s)
2001
The molecular basis of X-linked spondyloepiphyseal dysplasia tarda
Gedeon, A.
;
Tiller, G.
;
Le Merrer, M.
;
Heuertz, S.
;
Tranebjaerg, L.
;
Chitayat, D.
;
Robertson, S.
;
Glass, I.
;
Savarirayan, R.
;
Cole, W.
;
Rimoin, D.
;
Kousseff, B.
;
Ohashi, H.
;
Zabel, B.
;
Munnich, A.
;
Gecz, J.
;
Mulley, J.
2002
Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy
Stromme, P.
;
Mangelsdorf, M.
;
Shaw, M.
;
Lower, K.
;
Lewis, S.
;
Bruyere, H.
;
Lutcherath, V.
;
Gedeon, A.
;
Wallace, R.
;
Scheffer, I.
;
Turner, G.
;
Partington, M.
;
Frints, S.
;
Fryns, J.
;
Sutherland, G.
;
Mulley, J.
;
Gecz, J.
2008
Two novel JAK2 exon 12 mutations in JAK2V617F-negative polycythaemia vera patients
Butcher, C.
;
Hahn, U.
;
To, L.
;
Gecz, J.
;
Wilkins, E.
;
Scott, H.
;
Bardy, P.
;
D'Andrea, R.
2008
Restoring reproductive confidence in families with X-linked mental retardation by finding the causal mutation
Turner, G.
;
Boyle, J.
;
Partington, M.
;
Kerr, B.
;
Raymond, F.
;
Gecz, J.
Discover
Author
2
Gedeon, A.
2
Mulley, J.
2
Partington, M.
2
Turner, G.
1
Bardy, P.
1
Boyle, J.
1
Bruyere, H.
1
Butcher, C.
1
Chitayat, D.
1
Cole, W.
.
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Subject
4
Humans
3
Female
2
Genetic Linkage
2
Haplotypes
2
Molecular Sequence Data
2
X Chromosome
1
Adult
1
Amino Acid Sequence
1
Animals
1
Base Sequence
.
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Date issued
2
2008
1
2002
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2001