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R Oner

Showing results (11-20 of 38) with videos related to

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Hemoglobin|January 17, 2002
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patientE Birben, R Oner, C Oner, et al.
Hemoglobin|January 1, 1991
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation siteC Altay, A Gurgey, R Oner, et al.
Immunobiology|April 25, 2000
Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in TurkeyA I Berkel, E Birben, C Oner, et al.
International Journal of Biological Macromolecules|July 1, 1996
Investigation of ascorbate-Cu (II) induced cleavage of DNA by scanning tunneling microscopyM H Zareie, G Erdem, C Oner, 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.
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|May 12, 1998
HB H disease with homozygosity for red cell G6PD deficiency in a Turkish femaleC Oner, R Oner, E Birben, et al.
British Journal of Haematology|November 28, 2001
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap siteR Oner, C Oner, E Birben, et al.
Hematology and Cell Therapy|October 30, 1999
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patientA Koç, R Oner, C Oner, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
Hemoglobin|January 17, 2002
Homozygosity for Hb E-Saskatoon [beta22(B4)Glu-->Lys] in a Turkish patientE Birben, R Oner, C Oner, et al.
Hemoglobin|January 1, 1991
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation siteC Altay, A Gurgey, R Oner, et al.
Immunobiology|April 25, 2000
Molecular, genetic and epidemiologic studies on selective complete C1q deficiency in TurkeyA I Berkel, E Birben, C Oner, et al.
International Journal of Biological Macromolecules|July 1, 1996
Investigation of ascorbate-Cu (II) induced cleavage of DNA by scanning tunneling microscopyM H Zareie, G Erdem, C Oner, 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.
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|May 12, 1998
HB H disease with homozygosity for red cell G6PD deficiency in a Turkish femaleC Oner, R Oner, E Birben, et al.
British Journal of Haematology|November 28, 2001
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G-->A substitution at +22 relative to the beta-globin cap siteR Oner, C Oner, E Birben, et al.
Hematology and Cell Therapy|October 30, 1999
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patientA Koç, R Oner, C Oner, et al.
Pageof 4