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Results 1-6 of 6 (Search time: 0.001 seconds).
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Issue Date
Title
Author(s)
2013
A phase 2 trial of ponatinib in Philadelphia chromosome-positive leukemias
Cortes, J.E.
;
Kim, D.W.
;
Pinilla-Ibarz, J.
;
Le Coutre, P.
;
Paquette, R.
;
Chuah, C.
;
Nicolini, F.E.
;
Apperley, J.F.
;
Khoury, H.J.
;
Talpaz, M.
;
DiPersio, J.
;
DeAngelo, D.J.
;
Abruzzese, E.
;
Rea, D.
;
Baccarani, M.
;
Müller, M.C.
;
Gambacorti-Passerini, C.
;
Wong, S.
;
Lustgarten, S.
;
Rivera, V.M.
;
et al.
2013
Identification Of KLHL41 mutations implicates BTB-Kelch-Mediated Ubiquitination as an alternate pathway to myofibrillar disruption in nemaline myopathy
Gupta, V.
;
Ravenscroft, G.
;
Shaheen, R.
;
Todd, E.
;
Swanson, L.
;
Shiina, M.
;
Ogata, K.
;
Hsu, C.
;
Clarke, N.
;
Darras, B.
;
Farrar, M.
;
Hashem, A.
;
Manton, N.
;
Muntoni, F.
;
North, K.
;
Sandaradura, S.
;
Nishino, I.
;
Hayashi, Y.
;
Sewry, C.
;
Thompson, E.
;
et al.
2013
Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity
Cousminer, D.
;
Berry, D.
;
Timpson, N.
;
Ang, W.
;
Thiering, E.
;
Byrne, E.
;
Taal, H.
;
Huikari, V.
;
Bradfield, J.
;
Kerkhof, M.
;
Groen-Blokhuis, M.
;
Kreiner-Møller, E.
;
Marinelli, M.
;
Holst, C.
;
Leinonen, J.
;
Perry, J.
;
Surakka, I.
;
Kettunen, J.
;
Anttila, V.
;
Kaakinen, M.
;
et al.
2013
Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy
Braunlin, E.
;
Rosenfeld, H.
;
Kampmann, C.
;
Johnson, J.
;
Beck, M.
;
Giugliani, R.
;
Guffon, N.
;
Ketteridge, D.
;
Miranda, C.
;
Scarpa, M.
;
Schwartz, I.
;
Teles, E.
;
Wraith, J.
;
Barrios, P.
;
Dias da Silva, E.
;
Kurio, G.
;
Richardson, M.
;
Gildengorin, G.
;
Hopwood, J.
;
Imperiale, M.
;
et al.
2013
Rare variants in single-minded 1 (SIM1) are associated with severe obesity
Ramachandrappa, S.
;
Raimondo, A.
;
Cali, A.
;
Keogh, J.
;
Henning, E.
;
Saeed, S.
;
Thompson, A.
;
Garg, S.
;
Bochukova, E.
;
Brage, S.
;
Trowse, V.
;
Wheeler, E.
;
Sullivan, A.
;
Dattani, M.
;
Clayton, P.
;
Datta, V.
;
Bruning, J.
;
Wareham, N.
;
O'Rahilly, S.
;
Peet, D.
;
et al.
2013
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Dibbens, L.
;
de Vries, B.
;
Donatello, S.
;
Heron, S.
;
Hodgson, B.
;
Chintawar, S.
;
Crompton, D.
;
Hughes, J.
;
Bellows, S.
;
Klein, K.
;
Callenbach, P.
;
Corbett, M.
;
Gardner, A.
;
Kivity, S.
;
Iona, X.
;
Regan, B.
;
Weller, C.
;
Crimmins, D.
;
O'Brien, T.
;
Guerrero-Lopez, R.
;
et al.
Discover
Author
1
Abruzzese, E.
1
Ang, W.
1
Anttila, V.
1
Apperley, J.F.
1
Baccarani, M.
1
Barrios, P.
1
Beck, M.
1
Bellows, S.
1
Berry, D.
1
Bochukova, E.
.
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Subject
6
Female
6
Humans
5
Child
4
Young Adult
3
Adult
3
Child, Preschool
3
Gene Expression
3
Infant
2
Animals
2
Body Height
.
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