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| Preview | Issue Date | Title | Author(s) |
| 2004 | 1024C>T (R342X) is a recurrent RHF6 mutation also found in the original Börjeson-Forssman-Lehmann syndrome family | Lower, K.; Solders, G.; Bondeson, M.; Nelson, J.; Brun, A.; Crawford, J.; Malm, G.; Borjeson, M.; Turner, G.; Partington, M.; Gecz, J. |
| 2010 | 1210 Methodological approaches to conceptualizing and modeling the effect of dynamic family structure on child behavior | McDonald, S.; Moodie, E.; Lynch, J.; Satellite Symposia |
| 2012 | 14q12 and severe Rett-like phenotypes: new clinical insights and physical mapping of FOXG1-regulatory elements | Allou, L.; Lambert, L.; Amsallem, D.; Bieth, E.; Edery, P.; Destree, A.; Rivier, F.; Amor, D.; Thompson, E.; Nicholl, J.; Harbord, M.; Nemos, C.; Saunier, A.; Moustaine, A.; Vigouroux, A.; Jonveaux, P.; Philippe, C. |
| 2011 | 17-alpha-hydroxyprogesterone caproate for the prevention of adverse neonatal outcome in multiple pregnancies: A randomized controlled trial | Lim, A.; Schuit, E.; Bloemenkamp, K.; Bernardus, R.; Duvekot, J.; Erwich, J.; van Eyck, J.; Groenwold, R.; Hasaart, T.; Hummel, P.; Kars, M.; Kwee, A.; van Oirschot, C.; van Pampus, M.; Papatsonis, D.; Porath, M.; Spaanderman, M.; Willekes, C.; Wilpshaar, J.; Mol, B.; et al. |
| 2008 | 1D09C3, an mAb specific for MHC-II | Zola, H.; Beare, A. |
| 2015 | 236 effect of cyclic adenosine monophosphate modulator regulators in association with bmp15 on bovine embryo development in vitro | Machado, M.F.; Nogueira, M.F.; Gilchrist, R.B.; Sutton-McDowall, M.L.; Mottershead, D.G.; White, M.A.; Thompson, J.G.; : Australia) |
| 2014 | 25-hydroxyvitamin D concentrations in children with Crohn's disease supplemented with either 2000 or 400 IU daily for 6 months: a randomized controlled study | Wingate, K.; Jacobson, K.; Issenman, R.; Carroll, M.; Barker, C.; Israel, D.; Brill, H.; Weiler, H.; Barr, S.; Li, W.; Lyon, M.; Green, T. |
| 2011 | 4-aminobutyrate aminotrasferase (ABAT): genetic and pharmacological evidence for an involvement in gastro esophageal reflux disease | Jirholt, J.; Asling, B.; Hammond, P.; Davidson, G.; Knutsson, M.; Walentinsson, A.; Jensen, J.; Lehmann, A.; Agreus, L.; Lagerstrom-Fermer, M. |
| 2009 | A 1q44 deletion, paternal UPD of chromosome 2 and a deletion due to a complex translocation detected in children with abnormal phenotypes using new SNP array technology | Talseth-Palmer, B.; Bowden, N.; Meldrum, C.; Nicholl, J.; Thompson, E.; Friend, K.; Liebelt, J.; Bratkovic, D.; Haan, E.; Yu, S.; Scott, R. |
| 1996 | A 3-year follow-up of the intellectual and academic functioning of children receiving central nervous system prophylactic chemotherapy for leukemia | Brown, R.; Sawyer, M.; Antoniou, G.; Toogood, I.; Rice, M.; Thompson, N.; Madan-Swain, A. |
| 2012 | A bivalent Neisserie meningitidis recombinant lipidated factor H binding protein vaccine in young adults: results of a randomised, controlled, dose-escalation phase 1 trial | Richmond, P.; Nissen, M.; Marshall, H.; Lambert, S.; Roberton, D.; Gruber, W.; Jones, T.; Arora, A. |
| 2018 | A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers | Zhang, M.; Ferrari, R.; Tartaglia, M.C.; Keith, J.; Surace, E.I.; Wolf, U.; Sato, C.; Grinberg, M.; Liang, Y.; Xi, Z.; Dupont, K.; McGoldrick, P.; Weichert, A.; McKeever, P.M.; Schneider, R.; McCorkindale, M.D.; Manzoni, C.; Rademakers, R.; Graff-Radford, N.R.; Dickson, D.W.; et al. |
| 2015 | A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS | Rosmarin, D.; Palles, C.; Pagnamenta, A.; Kaur, K.; Pita, G.; Martin, M.; Domingo, E.; Jones, A.; Howarth, K.; Freeman-Mills, L.; Johnstone, E.; Wang, H.; Love, S.; Scudder, C.; Julier, P.; Fernández-Rozadilla, C.; Ruiz-Ponte, C.; Carracedo, A.; Castellvi-Bel, S.; Castells, A.; et al. |
| 2012 | A case series of five Sri Lankan patients with ovotesticular disorder of sex development | Wettasinghe, K.; Sirisena, N.; Andraweera, P.; Jayasekara, R.; Dissanayake, V. |
| 2012 | A clinical approach to the investigation of suspected vaccine anaphylaxis | Gold, M. |
| 1995 | A clinically mild case of mucopolysaccharidosis type I - Scheie syndrome (case report) | Kozlowski, K.; Nicol, R.; Hopwood, J. |
| 2004 | A combined 13CO2/H2 breath test can be used to assess starch digestion and fermentation in humans | Symonds, E.; Kritas, S.; Omari, T.; Butler, R. |
| 2005 | A common mitchondrial DNA variant is associated with thinness in mothers and their 20-yr-old offspring | Parker, E.; Phillips, D.; Cockington, R.; Cull, C.; Poulton, J. |
| 2006 | A comparison of booster immunisation with a combination DTPa-IPV vaccine or DTPa plus IPV in separate injections when co-administered with MMR, at age 4-6 years | Marshall, H.; Nolan, T.; Roberton, D.; Richmond, P.; Lambert, S.; Jacquet, J.; Schuerman, L. |
| 2010 | A comparison of oral narratives in children with specific language and non-specific language impairment | Pearce, W.; James, D.; McCormack, P. |
