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Issue Date
Title
Author(s)
2002
Recombinant Human Bone Morphogenetic Protein-2 for Treatment of Open Tibial Fractures
Csimma, C.
;
Genant, H.
;
Valentin-Opran, A.
;
Amit, Y.
;
Arbel, R.
;
Aro, H.
;
Atar, D.
;
Bishay, M.
;
Borner, M.
;
Chiron, P.
;
Choong, P.
;
Cinats, J.
;
Courtenay, B.
;
Feibel, R.
;
Geulette, B.
;
Gravel, C.
;
Haas, N.
;
Raschke, M.
;
Hammacher, E.
;
van der Velde, D.
;
et al.
2008
X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairment
Dibbens, L.
;
Tarpey, P.
;
Hynes, K.
;
Bayly, M.
;
Scheffer, I.
;
Smith, R.
;
Bomar, J.
;
Sutton, E.
;
Vandeleur, L.
;
Shoubridge, C.
;
Edkins, S.
;
Turner, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Jones, D.
;
et al.
2007
Epidemiological comparisons of problems and positive qualities reported by adolescents in 24 countries
Rescorla, L.
;
Achenbach, T.
;
Ivanova, M.
;
Dumenci, L.
;
Almqvist, F.
;
Bilenberg, N.
;
Bird, H.
;
Broberg, A.
;
Dobrean, A.
;
Dopfner, M.
;
Erol, N.
;
Forns, M.
;
Hannesdottir, H.
;
Kanbayashi, Y.
;
Lambert, M.
;
Leung, P.
;
Minaei, A.
;
Mulatu, M.
;
Novik, T.
;
Oh, K.
;
et al.
2006
Five-year follow-up of patients receiving imatinib for chronic myeloid leukemia
Druker, B.
;
Guilhot, F.
;
O'Brien, S.
;
Gathmann, I.
;
Kantarjian, H.
;
Gattermann, N.
;
Deininger, M.
;
Silver, R.
;
Goldman, J.
;
Stone, R.
;
Cervantes, F.
;
Hochhaus, A.
;
Powell, B.
;
Gabrilove, J.
;
Rousselot, P.
;
Reiffers, J.
;
Cornelissen, J.
;
Hughes, T.
;
Agis, H.
;
Fischer, T.
;
et al.
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.
2007
Mutations in UPF3B, a member of the nonsense-mediated mRNA decay complex, cause syndromic and nonsyndromic mental retardation
Tarpey, P.
;
Raymond, F.
;
Nguyen, L.
;
Rodriguez, J.
;
Hackett, A.
;
Vandeleur, L.
;
Smith, R.
;
Shoubridge, C.
;
Edkins, S.
;
Stevens, C.
;
O'Meara, S.
;
Tofts, C.
;
Barthorpe, S.
;
Buck, G.
;
Cole, J.
;
Halliday, K.
;
Hills, K.
;
Jones, D.
;
Mironenko, T.
;
Perry, J.
;
et al.
2009
Analyses of associations with asthma in four asthma population samples from Canada and Australia
Daly, D.
;
Lemire, M.
;
Akhabir, L.
;
Chan-Yeung, M.
;
He, J.
;
McDonald, T.
;
Stanford, A.
;
Stefanowicz, D.
;
Tripp, B.
;
Zamar, D.
;
Bosse, Y.
;
Ferretti, V.
;
Montpetit, A.
;
Tessier, M.
;
Becker, A.
;
Kozyrskyj, A.
;
Beilby, J.
;
McCaskie, P.
;
Musk, A.
;
Warrington, N.
;
et al.
2001
An enhanced linkage map of the sheep genome comprising more than 1000 loci
Maddox, J.
;
Davies, K.
;
Crawford, A.
;
Hulme, D.
;
Vaiman, D.
;
Cribiu, E.
;
Freking, B.
;
Beh, K.
;
Cockett, N.
;
Kang, N.
;
Riffkin, C.
;
Drinkwater, R.
;
Moore, S.
;
Dodds, K.
;
Lumsden, J.
;
van Stijn, T.
;
Phua, S.
;
Adelson, D.
;
Burkin, H.
;
Broom, J.
;
et al.
2009
Sequence variants in three loci influence monocyte counts and erythrocyte volume
Ferreira, M.
;
Hottenga, J.
;
Warrington, N.
;
Medland, S.
;
Willemsen, G.
;
Lawrence, R.
;
Gordon, S.
;
de Geus, E.
;
Henders, A.
;
Smit, J.
;
Campbell, M.
;
Wallace, L.
;
Evans, D.
;
Wright, M.
;
Nyholt, D.
;
James, A.
;
Beilby, J.
;
Penninx, B.
;
Palmer, L.
;
Frazer, I.
;
et al.
2009
Associations between CYP2D6 polymorphisms and outcomes among women with early stage breast cancer treated with Tamoxifen
Schroth, W.
;
Goetz, M.
;
Hamann, U.
;
Fasching, P.
;
Schmidt, M.
;
Winter, S.
;
Fritz, P.
;
Simon, W.
;
Suman, V.
;
Ames, M.
;
Safgren, S.
;
Kuffel, M.
;
Ulmer, H.
;
Bolander, J.
;
Strick, R.
;
Beckmann, M.
;
Koelbl, H.
;
Weinshilboum, R.
;
Ingle, J.
;
Eichelbaum, M.
;
et al.
Discover
Author
5
Edkins, S.
5
O'Meara, S.
5
Tarpey, P.
4
Barthorpe, S.
4
Buck, G.
4
Stevens, C.
3
Achenbach, T.
3
Almqvist, F.
3
Bilenberg, N.
3
Bird, H.
.
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Subject
40
Humans
34
Male
16
Middle Aged
12
Pedigree
10
Adult
10
Aged
10
Mutation
9
Genotype
8
Adolescent
8
Molecular Sequence Data
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