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Results 31-40 of 78 (Search time: 0.002 seconds).
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Issue Date
Title
Author(s)
2010
PHF6 mutations in T-cell acute lymphoblastic leukemia
Van Vlierberghe, P.
;
Palomero, T.
;
Khiabanian, H.
;
Van der Meulen, J.
;
Castillo, M.
;
Van Roy, N.
;
De Moerloose, B.
;
Philippe, J.
;
Gonzalez-Garcia, M.
;
Toribio, M.
;
Taghon, T.
;
Zuurbier, L.
;
Cauwelier, B.
;
Harrison, C.
;
Schwab, C.
;
Pisecker, M.
;
Strehl, S.
;
Langerak, A.
;
Gecz, J.
;
Sonneveld, E.
;
et al.
2011
Calculating the mean amplitude of glycemic excursion from continuous glucose monitoring data: An automated algorithm
Baghurst, P.
2010
Discrepancy in factor VIII 1-stage/2-stage activity in a child with Arg(531) -> His mutation
Nath, S.
;
Williams, V.
;
Griffiths, A.
;
Revesz, T.
2011
Clinical effects and treatment of envenoming by Hoplocephalus spp. snakes in Australia: Australian Snakebite Project (ASP-12)
Isbister, G.
;
White, J.
;
Currie, B.
;
O'Leary, M.
;
Brown, S.
2013
Gastroesophageal reflux, esophageal function, gastric emptying, and the relationship to dysphagia before and after antireflux surgery in children
Loots, C.
;
Van Herwaarden, M.
;
Benninga, M.
;
VanderZee, D.
;
van Wijk, M.
;
Omari, T.
2012
Comparison of intraabdominal abscess formation after laparoscopic and open appendicectomies in children
Nataraja, R.
;
Teague, W.
;
Galea, J.
;
Moore, L.
;
Haddad, M.
;
Tsang, T.
;
Khurana, S.
;
Clarke, S.
2013
Parental perspectives of vaccine safety and experience of adverse events following immunisation
Parrella, A.
;
Gold, M.
;
Marshall, H.
;
Braunack-Mayer, A.
;
Baghurst, P.
2010
CP or not CP? A review of diagnoses in a cerebral palsy register
Zarrinkalam, R.
;
Russo, R.
;
Gibson, C.
;
van Essen, P.
;
Peek, A.
;
Haan, E.
2010
Preemptive alloimmune intervention in high-risk pediatric acute lymphoblastic leukemia patients guided by minimal residual disease level before stem cell transplantation
Lankester, A.
;
Bierings, M.
;
van Wering, E.
;
Wijkhuijs, A.
;
de Weger, R.
;
Wijnen, J.
;
Vossen, J.
;
Versluys, B.
;
Egeler, R.
;
van Tol, M.
;
Putter, H.
;
Revesz, T.
;
van Dongen, J.
;
van der Velden, V.
;
Schilham, M.
2010
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay
Haan, E.
;
Gecz, J.
Discover
Author
11
Anderson, P.J.
11
Gecz, J.
10
Doyle, L.W.
10
et al.
7
Scheffer, I.
6
Cheong, J.L.Y.
6
Lee, K.J.
6
Revesz, T.
5
Dibbens, L.
4
Berkovic, S.
.
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77
Humans
62
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57
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37
Child, Preschool
31
Adolescent
22
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19
Infant
17
Infant, Newborn
13
Mutation
12
Australia
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