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Results 1-10 of 15 (Search time: 0.002 seconds).
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PreviewIssue DateTitleAuthor(s)
2013Incomplete request forms waste timeDeakin, Anita; Schultz, Timothy John; Mandel, Catherine J.
2013Problems with patient’s medical record numbersSchultz, Timothy John; Deakin, Anita; Mandel, Catherine J.
2012Does ovulation induction with follicle-stimulating hormone still have a future in polycystic ovary syndrome?Norman, R.
2014The effects of craniectomy compared to cranial vault remodeling on morphological, functional and neurological outcomes in infants with isolated non-syndromic sysnostosis of the sagittal suture: a systematic review protocolThwin, M.; Schultz, T.; Anderson, P.
2013RAB40AL loss-of-function mutation does not cause X-linked intellectual disabilityKalscheuer, V.; Iqbal, Z.; Hu, H.; Haas, S.; Shaw, M.; Lebrun, N.; Seemanova, E.; Voesenek, K.; Hobson, L.; Ropers, H.H.; Townshend, S.; Raynaud, M.; van Bokhoven, H.; Riazuddin, S.; Chelly, J.; Gecz, J.
2012New mutations and sporadic intellectual disabilityGecz, J.; Haan, E.
1998Temporal stability of acetylcholinesterase staining in colonic and rectal neural tissueByard, R.; Carli, M.
2014Contrast media reactions - to contrast or not to contrast?Deakin, Anita; Schultz, Timothy John; Mandel, Catherine J.
2014UPF3B gene and nonsense-mediated mRNA decay in autism spectrum disordersLaumonnier, F.; Nguyen, L.; Jolly, L.; Raynaud, M.; Gecz, J.; Patel, V.; Preedy, P.; Martin, C.
2014Nonsense-mediated mRNA decay: Inter-individual variability and human diseaseNguyen, L.; Wilkinson, M.; Gecz, J.