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A Gurgey

Showing results (41-50 of 51) with videos related to

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Journal of Chromatography|July 5, 1991
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetusesF Kutlar, H Moscoso, C R Kiefer, et al.
Hemoglobin|January 1, 1989
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemiaA Kutlar, F Kutlar, M Aksoy, et al.
Hemoglobin|January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemiaR Oner, S Agarwal, A J Dimovski, et al.
Acta Haematologica|January 1, 1992
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observationsY J Fei, R Oner, G Bözkurt, et al.
Biochemical and Biophysical Research Communications|June 16, 1988
Beta-thalassemia due to a T----A mutation within the ATA boxY J Fei, T A Stoming, G D Efremov, et al.
Blood|January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probesJ C Diaz-Chico, K G Yang, T A Stoming, et al.
Hemoglobin|January 1, 1990
Beta-thalassemia in TurkeyR Oner, C Altay, A Gurgey, et al.
Blood|December 3, 1998
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantationI Tezcan, W Xu, A Gurgey, et al.
Hemoglobin|January 1, 1986
Some notes about Hb Q-India and Hb Q-IranM Aksoy, A Gurgey, C Altay, et al.
Blood|May 1, 1989
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemiaJ M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
Journal of Chromatography|July 5, 1991
Quantities of adult, fetal and embryonic globin chains in the blood of eighteen- to twenty-week-old human fetusesF Kutlar, H Moscoso, C R Kiefer, et al.
Hemoglobin|January 1, 1989
Beta-thalassemia intermedia in two Turkish families is caused by the interaction of Hb Knossos [beta 27(B9)Ala----Ser] and of Hb City of Hope [beta 69(E13)Gly----ser] with beta (0)-thalassemiaA Kutlar, F Kutlar, M Aksoy, et al.
Hemoglobin|January 1, 1991
The G----A mutation at position +22 3' to the Cap site of the beta-globin gene as a possible cause for a beta-thalassemiaR Oner, S Agarwal, A J Dimovski, et al.
Acta Haematologica|January 1, 1992
Hb H disease caused by a homozygosity for the AATAAA-->AATAAG mutation in the polyadenylation site of the alpha 2-globin gene: hematological observationsY J Fei, R Oner, G Bözkurt, et al.
Biochemical and Biophysical Research Communications|June 16, 1988
Beta-thalassemia due to a T----A mutation within the ATA boxY J Fei, T A Stoming, G D Efremov, et al.
Blood|January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probesJ C Diaz-Chico, K G Yang, T A Stoming, et al.
Hemoglobin|January 1, 1990
Beta-thalassemia in TurkeyR Oner, C Altay, A Gurgey, et al.
Blood|December 3, 1998
Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantationI Tezcan, W Xu, A Gurgey, et al.
Hemoglobin|January 1, 1986
Some notes about Hb Q-India and Hb Q-IranM Aksoy, A Gurgey, C Altay, et al.
Blood|May 1, 1989
A C----T substitution at nt--101 in a conserved DNA sequence of the promotor region of the beta-globin gene is associated with "silent" beta-thalassemiaJ M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.
Pageof 6