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Issue Date
Title
Author(s)
2004
Interleukin 18 receptor
Sergi, B.
;
Penttila, I.
2007
Mutations in ZDHHC9, which encodes a palmitoyltransferase of NRAS and HRAS, cause X-linked mental retardation associated with a marfanoid habitus
Raymond, F.
;
Tarpey, P.
;
Edkins, S.
;
Tofts, C.
;
O'Meara, S.
;
Teague, J.
;
Butler, A.
;
Stevens, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Dicks, E.
;
Gray, K.
;
Harrison, R.
;
Hills, K.
;
Hinton, J.
;
Jones, D.
;
Menzies, A.
;
Perry, J.
;
Raine, K.
;
et al.
2000
Molecular cloning and characterisation of GPR74 a novel G-protein coupled receptor closest related to the Y-receptor family
Parker, R.
;
Copeland, N.
;
Eyre, H.
;
Liu, M.
;
Gilbert, D.
;
Crawford, J.
;
Couzens, M.
;
Sutherland, G.
;
Jenkins, N.
;
Herzog, H.
2000
Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DDP) IV homolog, DPP8
Abbott, C.
;
Yu, D.
;
Woollatt, E.
;
Sutherland, G.
;
McCaughan, G.
;
Gorrell, M.
2001
HPP1: A transmembrane protein-encoding gene commonly methylated in colorectal polyps and cancers
Young, J.
;
Biden, K.
;
Simms, L.
;
Huggard, P.
;
Karamatic, R.
;
Eyre, H.
;
Sutherland, G.
;
Herath, N.
;
Barker, M.
;
Anderson, G.
;
Fitzpatrick, D.
;
Ramm, G.
;
Jass, J.
;
Leggett, B.
2005
Twenty-six novel EFNB1 mutations in familial and sporadic craniofrontonasal syndrome (CFNS)
Wieland, I.
;
Reardon, W.
;
Jakubiczka, S.
;
Franco, B.
;
Kress, W.
;
Vincent-Delorme, C.
;
Theirry, P.
;
Edwards, M.
;
Konig, R.
;
Rusu, C.
;
Schweiger, S.
;
Thompson, E.
;
Tinschert, S.
;
Stewart, F.
;
Wieacker, P.
2007
Extended spectrum of idiopathic generalized epilepsies associated with CACNA1H functional variants
Heron, S.
;
Khosravani, H.
;
Varela, D.
;
Bladen, C.
;
Williams, T.
;
Newman, M.
;
Scheffer, I.
;
Berkovic, S.
;
Mulley, J.
;
Zamponi, G.
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
Fragile XE-associated familial mental retardation protein 2 (FMR2) acts as a potent transcription activator
Hillman, M.
;
Gecz, J.
Discover
Author
12
Gecz, J.
10
Sutherland, G.
7
Eyre, H.
6
et al.
6
Hopwood, J.
4
Fryns, J.
3
Baker, E.
3
Brooks, D.
3
Edkins, S.
3
Kalscheuer, V.
.
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Subject
37
Humans
34
Molecular Sequence Data
16
Animals
15
Base Sequence
14
Male
14
Mutation
13
Sequence Homology, Amino Acid
12
Female
12
Mice
11
Pedigree
.
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Date issued
1
2009
1
2008
5
2007
3
2006
1
2005
8
2004
4
2003
3
2002
8
2001
5
2000
.
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