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The Turkish Journal of Pediatrics|July 1, 1993
Prenatal diagnosis of sickle cell anemia using PCR and restriction enzyme Dde IA Gürgey, S Beksaç, L Mesci, et al.Clinical Genetics|May 1, 1997
Analysis of 65 Turkish patients with congenital aplastic anemia (Fanconi anemia and non-Fanconi anemia): Hacettepe experienceC Altay, M Alikaşifoglu, A Kara, et al.International Journal of Pediatric Otorhinolaryngology|January 1, 1994
Audiologic and impedancemetric findings within thalassaemic patientsM Onerci, S Aslan, F Gümrük, et al.JBR-BTR : Organe De La Societe Royale Belge De Radiologie (SRBR) = Orgaan Van De Koninklijke Belgische Vereniging Voor Radiologie (KBVR)|January 22, 2015
Diffusion-weighted MR imaging: role in the differential diagnosis of breast lesionsC Altay, P Balci, S Altay, et al.Pediatric Hematology and Oncology|January 15, 2002
Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patientR Oner, C Acar, C Oner, et al.Pediatric Hematology and Oncology|March 1, 1995
Congenital hypoplastic anemia in six patients: unusual association of short proximal phalanges with mild anemiaM Cetin, A Kara, A Gürgey, et al.Hemoglobin|January 1, 1997
The molecular basis of Hb H disease in TurkeyC Oner, A Gürgey, R Oner, et al.British Journal of Haematology|February 1, 1997
Molecular analysis of the Turkish form of deletion-inversion (delta beta)(0) thalassaemiaC Oner, R Oner, H Balkan, et al.Hemoglobin|January 1, 1981
Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotesG Dincol, C Altay, M Aksoy, et al.International Journal of Clinical Practice|September 20, 2007
Trial of a new pain assessment tool in patients with low education: the full cup testU Ergün, B Say, G Ozer, et al.Pageof 16