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Saudi Medical Journal|September 9, 2016
Genetic disorders in Arabs as for OMIMG O Tadmouri, N Bissar-TadmouriHuman Biology|April 1, 1997
Rare beta-thalassemia mutation in a Turkish patient: FSC-36/37 (-T)G O Tadmouri, S Tüzmen, A N BaşakAmerican Journal of Hematology|September 2, 1998
HbS/beta(del)-thalassemia associated with high levels of hemoglobins A2 and F in a Turkish familyG O Tadmouri, L Yüksel, A N BaşakThe Cochrane Database of Systematic Reviews|April 20, 2007
Piracetam for reducing the incidence of painful sickle cell disease crisesA A Al Hajeri, Z Fedorowicz, A Omran, et al.Human Biology|January 5, 2002
History and origin of beta-thalassemia in Turkey: sequence haplotype diversity of beta-globin genesG O Tadmouri, N Garguier, J Demont, et al.American Journal of Hematology|March 8, 2000
A rare mutation [IVS-I-130 (G-A)] in a Turkish beta-thalassemia major patientG O Tadmouri, O Bilenoğlu, S Kantarci, et al.Human Biology|May 1, 1999
Identification of the Chinese IVS-II-654 (C-->T) beta-thalassemia mutation in an immigrant Turkish family: recurrence or migration?G O Tadmouri, O Bilenoğlu, F Kutlar, et al.Prenatal Diagnosis|March 1, 1996
Prenatal diagnosis of beta-thalassaemia and sickle cell anaemia in TurkeyS Tüzmen, G O Tadmouri, A Ozer, et al.American Journal of Hematology|March 12, 1998
Molecular and population genetic analyses of beta-thalassemia in TurkeyG O Tadmouri, S Tüzmen, H Ozçelik, et al.Clinical Genetics|May 27, 2015
Comorbidity in the Tunisian populationL Romdhane, O Messaoud, Y Bouyacoub, et al.Pageof 1