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Results: 1-15 |
Results: 15

Authors: Challen, K Harris, HJ Harris, R Modell, B Ponder, B
Citation: K. Challen et al., Confidential inquiries should be funded in clinical genetics, BR MED J, 322(7293), 2001, pp. 1061-1061

Authors: Modell, B Khan, M Darlison, M King, A Layton, M Old, J Petrou, M Varnavides, L
Citation: B. Modell et al., A national register for surveillance of inherited disorders: beta thalassaemia in the United Kingdom, B WHO, 79(11), 2001, pp. 1006-1013

Authors: Modell, M Khan, M Modell, B Wonke, B
Citation: M. Modell et al., Why do some practices respond to an educational intervention? (vol 50, pg 826, 2000), BR J GEN PR, 50(461), 2000, pp. 1009-1009

Authors: Modell, M Khan, M Modell, B Wonke, B
Citation: M. Modell et al., Why do some practices respond to an educational intervention?, BR J GEN PR, 50(459), 2000, pp. 826-827

Authors: Modell, B Harris, R Lane, B Khan, M Darlison, M Petrou, M Old, J Layton, M Varnavides, L
Citation: B. Modell et al., Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry, BR MED J, 320(7231), 2000, pp. 337-341

Authors: Rajab, AG Patton, MA Modell, B
Citation: Ag. Rajab et al., Study of hemoglobinopathies in Oman through a national register, SAUDI MED J, 21(12), 2000, pp. 1168-1172

Authors: Petrou, M Modell, B Shetty, S Khan, M Ward, RHT
Citation: M. Petrou et al., Long-term effect of prospective detection of high genetic risk on couples'reproductive life: data for thalassaemia, PRENAT DIAG, 20(6), 2000, pp. 469-474

Authors: Ahmed, S Saleem, M Sultana, N Raashid, Y Waqar, A Anwar, M Modell, B Karamat, KA Petrou, M
Citation: S. Ahmed et al., Prenatal diagnosis of beta-thalassaemia in Pakistan: experience in a Muslim country, PRENAT DIAG, 20(5), 2000, pp. 378-383

Authors: Old, J Petrou, M Varnavides, L Layton, M Modell, B
Citation: J. Old et al., Accuracy of prenatal diagnosis for haemoglobin disorders in the UK: 25 years' experience, PRENAT DIAG, 20(12), 2000, pp. 986-991

Authors: Modell, B Khan, M Darlison, M
Citation: B. Modell et al., Survival in beta-thalassaemia major in the UK: data from the UK thalassaemia register, LANCET, 355(9220), 2000, pp. 2051-2052

Authors: Harris, R Lane, B Harris, H Williamson, P Dodge, J Modell, B Ponder, B Rodeck, C Alberman, E
Citation: R. Harris et al., National Confidential Enquiry into counselling for genetic disorders by non-geneticists: general recommendations and specific standards for improvingcare, BR J OBST G, 106(7), 1999, pp. 658-663

Authors: Gill, PS Modell, B
Citation: Ps. Gill et B. Modell, Thalassaemia among Asians in Britain - Reply, BR MED J, 318(7187), 1999, pp. 873-873

Authors: Karnon, J Zeuner, D Brown, J Ades, AE Wonke, B Modell, B
Citation: J. Karnon et al., Lifetime treatment costs of beta-thalassaemia major, CLIN LAB H, 21(6), 1999, pp. 377-385

Authors: Hickman, M Modell, B Greengross, P Chapman, C Layton, M Falconer, S Davies, SC
Citation: M. Hickman et al., Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic-specific rates, BR J HAEM, 104(4), 1999, pp. 860-867

Authors: Modell, M Modell, B
Citation: M. Modell et B. Modell, Reproductive information and advice in primary care, OX GEN PRAC, 43, 1999, pp. 271-289
Risultati: 1-15 |