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Hemoglobin
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March 18, 2000
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family
F Gümrük, H Mergen, R Oner, et al.
Hemoglobin
|
January 17, 2002
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype
E Birben, C Oner, R Oner, et al.
Haematologica
|
March 1, 1992
Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemia
M C Rosatelli, C Altay, R Oner, et al.
British Journal of Haematology
|
October 1, 1991
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene
R Oner, C Oner, J B Wilson, et al.
Hemoglobin
|
September 7, 2000
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels
R Oner, E Birben, C Acar, et al.
The Turkish Journal of Pediatrics
|
April 1, 1997
Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutation
A Gürgey, H Balkan, G Irken, et al.
Hemoglobin
|
January 1, 1991
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians
S Fattoum, F Guemira, C Oner, et al.
American Journal of Hematology
|
July 30, 2004
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family
M Sözen, C Karaaslan, R Oner, et al.
Human Genetics
|
January 1, 1994
The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed
V Divoky, E Baysal, R Oner, et al.
Acta Haematologica
|
January 1, 1996
A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family
R Oner, C Oner, G Erdem, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 4
Hemoglobin
|
March 18, 2000
Beta-thalassemia intermedia associated with homozygosity for the -87 (C-->T) mutation in a Turkish family
F Gümrük, H Mergen, R Oner, et al.
Hemoglobin
|
January 17, 2002
Severe beta-thalassemia in frameshift codon 6 (-A) homozygotes: effects of haplotype on phenotype
E Birben, C Oner, R Oner, et al.
Haematologica
|
March 1, 1992
Beta-globin haplotype and XmnI polymorphism at position G (gamma)-158 and HbF production in Fanconi's anemia
M C Rosatelli, C Altay, R Oner, et al.
British Journal of Haematology
|
October 1, 1991
Dominant beta-thalassaemia trait in a Portuguese family is caused by a deletion of (G)TGGCTGGTGT(G) and an insertion of (G)GCAG(G) in codons 134, 135, 136 and 137 of the beta-globin gene
R Oner, C Oner, J B Wilson, et al.
Hemoglobin
|
September 7, 2000
Molecular analysis of turkish beta-thalassemia heterozygotes with normal Hb A2 levels
R Oner, E Birben, C Acar, et al.
The Turkish Journal of Pediatrics
|
April 1, 1997
Compound heterozygosity for hemoglobin Knossos [alpha 2 beta 2 27 (B9) Ala-Ser] and IVS I-1 mutation
A Gürgey, H Balkan, G Irken, et al.
Hemoglobin
|
January 1, 1991
Beta-thalassemia, HB S-beta-thalassemia and sickle cell anemia among Tunisians
S Fattoum, F Guemira, C Oner, et al.
American Journal of Hematology
|
July 30, 2004
Severe hemolytic anemia associated with Hb Volga [beta27(B9)Ala-->Asp]: GCC-->GAC at codon 27 in a Turkish family
M Sözen, C Karaaslan, R Oner, et al.
Human Genetics
|
January 1, 1994
The T-->C mutation at position +96 of the untranslated region 3' to the terminating codon of the beta-globin gene is a rare polymorphism that does not cause a beta-thalassemia as previously ascribed
V Divoky, E Baysal, R Oner, et al.
Acta Haematologica
|
January 1, 1996
A novel (delta beta)(0)-thalassemia due to a approximately 30-kb deletion observed in a Turkish family
R Oner, C Oner, G Erdem, et al.
Page
of 4