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F Kutlar

Showing results (51-60 of 89) with videos related to

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British Journal of Haematology|September 1, 1986
Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observationsJ R Aluoch, Y Kilinç, M Aksoy, et al.
British Journal of Haematology|February 1, 1987
Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from KenyaP J Ojwang, T Ogada, P Beris, et al.
Hemoglobin|January 1, 1988
Biochemical and molecular aspects of beta-thalassemia types in northern SardiniaB Masala, L Manca, D Gallisai, et al.
Hemoglobin|January 1, 1988
Characterization of abnormalities in the gamma-globin gene arrangements of Japanese newbornsT Harano, K Harano, M Ukita, et al.
Blood|January 1, 1989
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin geneT A Stoming, G S Stoming, K D Lanclos, et al.
American Journal of Hematology|September 1, 1991
Molecular characterization of Hb S(C) beta-thalassemia in American blacksJ M Gonzalez-Redondo, A Kutlar, F Kutlar, et al.
Acta Haematologica|January 1, 1990
Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia alleleJ Codrington, J Anijs, J H Wisse, et al.
Human Genetics|May 1, 1989
The levels of zeta, gamma, and delta chains in patients with Hb H diseaseF Kutlar, J M Gonzalez-Redondo, A Kutlar, et al.
British Journal of Haematology|January 1, 1989
Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin geneJ M Gonzalez-Redondo, T A Stoming, F Kutlar, et al.
American Journal of Hematology|October 1, 1992
Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobinP Beris, M N Kitundu, E Baysal, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
British Journal of Haematology|September 1, 1986
Sickle cell anaemia among Eti-Turks: haematological, clinical and genetic observationsJ R Aluoch, Y Kilinç, M Aksoy, et al.
British Journal of Haematology|February 1, 1987
Haplotypes and alpha globin gene analyses in sickle cell anaemia patients from KenyaP J Ojwang, T Ogada, P Beris, et al.
Hemoglobin|January 1, 1988
Biochemical and molecular aspects of beta-thalassemia types in northern SardiniaB Masala, L Manca, D Gallisai, et al.
Hemoglobin|January 1, 1988
Characterization of abnormalities in the gamma-globin gene arrangements of Japanese newbornsT Harano, K Harano, M Ukita, et al.
Blood|January 1, 1989
An A gamma type of nondeletional hereditary persistence of fetal hemoglobin with a T----C mutation at position -175 to the cap site of the A gamma globin geneT A Stoming, G S Stoming, K D Lanclos, et al.
American Journal of Hematology|September 1, 1991
Molecular characterization of Hb S(C) beta-thalassemia in American blacksJ M Gonzalez-Redondo, A Kutlar, F Kutlar, et al.
Acta Haematologica|January 1, 1990
Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia alleleJ Codrington, J Anijs, J H Wisse, et al.
Human Genetics|May 1, 1989
The levels of zeta, gamma, and delta chains in patients with Hb H diseaseF Kutlar, J M Gonzalez-Redondo, A Kutlar, et al.
British Journal of Haematology|January 1, 1989
Severe Hb S-beta zero-thalassaemia with a T----C substitution in the donor splice site of the first intron of the beta-globin geneJ M Gonzalez-Redondo, T A Stoming, F Kutlar, et al.
American Journal of Hematology|October 1, 1992
Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobinP Beris, M N Kitundu, E Baysal, et al.
Pageof 9