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Issue Date
Title
Author(s)
1995
Expression, purification and characterization of recombinant human N-acetylgalactosamine-6-sulphatase
Bielicki, J.
;
Fuller, M.
;
Guo, X.H.
;
Morris, C.
;
Hopwood, J.
;
Anson, D.
1995
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation
Hunt, C.
;
Eyre, H.
;
Akkari, P.
;
Meredith, C.
;
Dorosz, S.
;
Wilton, S.
;
Callen, D.
;
Laing, N.
;
Baker, E.
2006
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
Hagens, O.
;
Dubos, A.
;
Abidi, F.
;
Barbi, G.
;
Van Zutven, L.
;
Hoeltzenbein, M.
;
Tommerup, N.
;
Moraine, C.
;
Fryns, J.
;
Chelly, J.
;
van Bokhoven, H.
;
Gecz, J.
;
Dollfus, H.
;
Ropers, H.
;
Schwartz, C.
;
de Cassia Stocco dos Santos, R.
;
Kalscheuer, V.
;
Hanauer, A.
2000
Gene encoding the mouse sulphamidase: cDNA cloning, structure, and chromosomal mapping
Costanzi, E.
;
Beccari, T.
;
Stinchi, S.
;
Bibi, L.
;
Hopwood, J.
;
Orlacchio, A.
2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome
Heron, S.
;
Grinton, B.
;
Kivity, S.
;
Afawi, Z.
;
Zuberi, S.
;
Hughes, J.
;
Pridmore, C.
;
Hodgson, B.
;
Iona, X.
;
Sadleir, L.
;
Pelekanos, J.
;
Herlenius, E.
;
Goldberg-Stern, H.
;
Bassan, H.
;
Haan, E.
;
Korczyn, A.
;
Gardner, A.
;
Corbett, M.
;
Gecz, J.
;
Thomas, P.
;
et al.
2010
Mutations in the small GTPase gene RAB39B are responsible for X-linked mental retardation associated with autism, epilepsy, and macrocephaly
Giannandrea, M.
;
Bianchi, V.
;
Mignogna, M.
;
Sirri, A.
;
Carrabino, S.
;
D'Elia, E.
;
Vecellio, M.
;
Russo, S.
;
Cogliati, F.
;
Larizza, L.
;
Ropers, H.
;
Tzschach, A.
;
Kalscheuer, V.
;
Oehl-Jaschkowitz, B.
;
Skinner, C.
;
Schwartz, C.
;
Gecz, J.
;
Van Esch, H.
;
Raynaud, M.
;
Chelly, J.
;
et al.
2001
Fcα/μ receptor is a single gene-family member closely related to polymeric immunoglobulin receptor encoded on Chromosome 1
Shimizu, Y.
;
Honda, S.
;
Yotsumoto, K.
;
Tahara-Hanaoka, S.
;
Eyre, H.
;
Sutherland, G.
;
Endo, Y.
;
Shibuya, K.
;
Koyama, A.
;
Nakauchi, H.
;
Shibuya, A.
1995
Localisation of the adenosine A2b receptor subtype (ADORA2B) to chromosome 17p11.2-p12 by FISH and PCR screening of somatic cell hybrids
Townsend-Nicholson, A.
;
Baker, E.
;
Sutherland, G.
;
Schofield, P.
1995
The CEPH consortium linkage map of human chromosome 16
Kozman, H.
;
Keith, T.
;
Donis-Keller, H.
;
White, R.
;
Weissenbach, J.
;
Sutherland, G.
2004
HLS5, a novel RBCC (ring finger, B box, coiled-coil) family member isolated from a hemopoietic lineage switch, is a candidate tumor suppressor
Lalonde, J.
;
Lim, R.
;
Ingley, E.
;
Tilbrook, P.
;
Thompson, M.
;
McCulloch, R.
;
Beaumont, J.
;
Wicking, C.
;
Eyre, H.
;
Sutherland, G.
;
Howe, K.
;
Solomon, E.
;
Williams, J.
;
Klinken, S.
Discover
Author
22
Sutherland, G.
9
Eyre, H.
8
Baker, E.
7
Hopwood, J.
6
Gecz, J.
5
Callen, D.
4
Nicholl, J.
3
Brooks, D.
3
Copeland, N.
3
Crawford, J.
.
next >
Subject
36
Molecular Sequence Data
22
Amino Acid Sequence
22
Mice
21
Chromosome Mapping
17
DNA, Complementary
14
DNA Primers
14
Male
12
Cloning, Molecular
11
In Situ Hybridization, Fluorescence
11
Sequence Homology, Amino Acid
.
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Date issued
4
2010 - 2012
10
2000 - 2009
28
1994 - 1999