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Results: 1-9 |
Results: 9

Authors: Dawson, LE Pham, B Hunter, AGW
Citation: Le. Dawson et al., Low rate of adequate folic acid supplementation in well-educated women of high socioeconomic status attending a genetics clinic, CAN MED A J, 164(8), 2001, pp. 1149-1150

Authors: Hunter, AGW Sharpe, N Mullen, M Meschino, WS
Citation: Agw. Hunter et al., Ethical, legal, and practical concerns about recontacting patients to inform them of new information: The case in medical genetics, AM J MED G, 103(4), 2001, pp. 265-276

Authors: Stern, HS Viertelhausen, S Hunter, AGW O'Rourke, K Cappelli, M Perras, H Serfas, K Blumenthall, A Dewar, D Baumann, E Lagarde, AE
Citation: Hs. Stern et al., APC I1304K increases risk of transition from polyp to colorectal carcinomain Ashkenazi jews, GASTROENTY, 120(2), 2001, pp. 392-400

Authors: Hunter, AGW
Citation: Agw. Hunter, Outcome of the routine assessment of patients with mental retardation in agenetics clinic, AM J MED G, 90(1), 2000, pp. 60-68

Authors: Armour, CM Bulman, DE Hunter, AGW
Citation: Cm. Armour et al., Clinical and radiological assessment of a family with mild brachydactyly type A1: the usefulness of metacarpophalangeal profiles, J MED GENET, 37(4), 2000, pp. 292-296

Authors: Humphreys, L Hunter, AGW Zimak, A O'Brien, A Korneluk, Y Cappelli, M
Citation: L. Humphreys et al., Why patients do not attend for their appointments at a genetics clinic, J MED GENET, 37(10), 2000, pp. 810-815

Authors: Gilpin, CA Carson, N Hunter, AGW
Citation: Ca. Gilpin et al., A preliminary validation of a family history assessment form to select women at risk for breast or ovarian cancer for referral to a genetics center, CLIN GENET, 58(4), 2000, pp. 299-308

Authors: Hunter, AGW
Citation: Agw. Hunter, A pilot study of the possible role of familial defects in anticoagulation as a cause for terminal limb reduction malformations, CLIN GENET, 57(3), 2000, pp. 197-204

Authors: Hunter, AGW
Citation: Agw. Hunter, Perceptions of the outcome of orthopedic surgery in patients with chondrodysplasias, CLIN GENET, 56(6), 1999, pp. 434-440
Risultati: 1-9 |