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| Preview | Issue Date | Title | Author(s) |
| 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. |
| 1999 | A comparison of parent and adolescent reports describing the health-related quality of life of adolescents treated for cancer | Sawyer, M.; Antoniou, G.; Toogood, I.; Rice, M. |
| 2015 | A comparison of two methods for estimating 50% of the maximal motor evoked potential | Pitcher, J.; Doeltgen, S.; Goldsworthy, M.; Schneider, L.; Vallence, A.; Smith, A.; Semmler, J.; McDonnell, M.; Ridding, M. |
| 2005 | A comparison of Verotoxin B-subunit (Stx1B) and CD77 antibody to define germinal centre populations | Bailey, S.; Mardell, C.; Wheatland, L.; Zola, H.; Macardle, P. |
| 2002 | A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction | Callen, D.; Eyre, H.; McDonnell, S.; Schuffenhauer, S.; Bhalla, K. |
| 2013 | A complicated case of plagiocephaly followed by delayed craniosynostosis | Moore, J.M.; Molly, C.; Anderson, P.J. |
| 2007 | A cross-sectional survey to assess community attitudes to introduction of human papillomavirus vaccine | Marshall, H.; Ryan, P.; Roberton, D.; Baghurst, P. |
| 1996 | A decade of gastroschisis in the era of antenatal ultrasound | Nicholls, E.; Ford, W.; Barnes, K.; Furness, M.; Hayward, C. |
| 2010 | A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C | Jensen, L.; Bartenschlager, H.; Rujirabanjerd, S.; Tzschach, A.; Numann, A.; Janecke, A.; Sporle, R.; Stricker, S.; Raynaud, M.; Nelson, J.; Hackett, A.; Fryns, J.; Chelly, J.; de Brouwer, A.; Hamel, B.; Gecz, J.; Ropers, H.; Kuss, A. |
