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BMJ (Clinical Research Ed.)|February 20, 1993
What proportion of congenital abnormalities can be prevented?A E Czeizel, Z Intôdy, B ModellBritish Medical Journal|September 23, 1972
Incidence of -thalassaemia trait among Cypriots in LondonC B Modell, A Benson, C R WrightBritish Medical Journal|June 7, 1980
Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia majorB Modell, R H Ward, D V FairweatherBritish Journal of Obstetrics and Gynaecology|February 1, 1980
Obstetric aspects of midtrimester fetal blood sampling by needling or fetoscopyD V Fairweather, R H Ward, B ModellBulletin of the World Health Organization|January 1, 1995
Prevention and control of haemoglobinopathiesM Angastiniotis, B Modell, P Englezos, et al.Saudi Medical Journal|May 22, 2001
Study of hemoglobinopathies in Oman through a national registerA G Rajab, M A Patton, B ModellJournal of Medical Genetics|November 1, 1992
Factors affecting the uptake of prenatal diagnosis for sickle cell diseaseM Petrou, M Brugiatelli, R H Ward, et al.Prenatal Diagnosis|December 13, 2000
Accuracy of prenatal diagnosis for haemoglobin disorders in the UK: 25 years' experienceJ Old, M Petrou, L Varnavides, et al.British Journal of Obstetrics and Gynaecology|March 1, 1979
Antenatal search for fetal beta-thalassaemia in a twin pregnancyH Ward, M Matsakis, M Mouzouras, et al.Scandinavian Journal of Clinical and Laboratory Investigation|March 17, 2007
Microcytosis, iron deficiency and thalassaemia in a multi-ethnic community: a pilot studyB Wonke, M Modell, T Marlow, et al.Pageof 139