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Results 1-10 of 20 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2004
Interleukin 18 receptor
Sergi, B.
;
Penttila, I.
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.
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.
2000
Y-receptor-like genes GPR72 and GPR73: molecular cloning, genomic organisation and assignment to human chromosome 11q21.1 and 2p14 and mouse chromosome 9 and 6
Parker, R.
;
Liu, M.
;
Eyre, H.
;
Copeland, N.
;
Gilbert, D.
;
Crawford, J.
;
Sutherland, G.
;
Jenkins, N.
;
Herzog, H.
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.
2004
Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation
Weaving, L.
;
Christodoulou, J.
;
Williamson, S.
;
Friend, K.
;
McKenzie, O.
;
Archer, H.
;
Evans, J.
;
Clarke, A.
;
Pelka, G.
;
Tam, P.
;
Watson, C.
;
Lahooti, H.
;
Ellaway, C.
;
Bennetts, B.
;
Leonard, H.
;
Gecz, J.
2003
Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation
Burdon, K.
;
McKay, J.
;
Sale, M.
;
Russell-Eggitt, I.
;
Mackey, D.
;
Wirth, G.
;
Elder, J.
;
Nicoll, A.
;
Clarke, M.
;
FitzGerald, L.
;
Stankovich, J.
;
Shaw, M.
;
Sharma, S.
;
Gajovic, S.
;
Gruss, P.
;
Ross, S.
;
Thomas, P.
;
Voss, A.
;
Thomas, T.
;
Gecz, J.
;
et al.
2001
A novel missense mutation in lysosomal sulfamidase is the basis of MPS III A in a spontaneous mouse mutant
Bhattacharyya, R.
;
Gliddon, B.
;
Beccari, T.
;
Hopwood, J.
;
Stanley, P.
2004
Immunoneutralization of growth differentiation factor 9 reveals it partially accounts for mouse oocyte mitogenic activity
Gilchrist, R.
;
Ritter, L.
;
Cranfield, M.
;
Jeffrey, L.
;
Amato, F.
;
Scott, S.
;
Myllymaa, S.
;
Kaivo-Oja, N.
;
Lankinen, H.
;
Mottershead, D.
;
Groome, N.
;
Ritvos, O.
Discover
Author
5
Hopwood, J.
5
Sutherland, G.
4
Eyre, H.
3
Beccari, T.
3
Gecz, J.
2
Costanzi, E.
2
Gliddon, B.
2
Orlacchio, A.
1
Abidi, F.
1
Aisa, M.
.
next >
Subject
20
Animals
14
Humans
13
Amino Acid Sequence
9
Base Sequence
6
Female
5
Chromosome Mapping
5
DNA, Complementary
5
Male
5
Sequence Alignment
5
Sequence Analysis, DNA
.
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