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Blood
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January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes
J C Diaz-Chico, K G Yang, T A Stoming, et al.
Hemoglobin
|
January 1, 1988
Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg]
M A Ali, P Pinkerton, S W Chow, 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-thalassemia
J M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.
American Journal of Hematology
|
December 1, 1993
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients
M A Cürük, A J Dimovski, E Baysal, et al.
Blood
|
May 1, 1990
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions
J B Wilson, B B Webber, H Hu, et al.
American Journal of Hematology
|
March 1, 1993
Spleen in sickle cell anemia: comparative studies of Nigerian and U.S. patients
A D Adekile, K M McKie, O O Adeodu, et al.
Hemoglobin
|
January 1, 1988
Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant
J J Malcorra-Azpiazu, M I Balda-Aguirre, J C Diaz-Chico, et al.
Blood
|
September 1, 1988
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
J M Gonzalez-Redondo, T A Stoming, K D Lanclos, et al.
British Journal of Haematology
|
March 1, 1988
Variation in clinical severity among patients with Hb Lepore-Boston-beta-thalassaemia is related to the type of beta-thalassaemia
D G Efremov, G D Efremov, N Zisovski, et al.
Page
of 9
Search research articles
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Showing results (81-90 of 89) with videos related to
Sort By:
Page
of 9
You have reached the last page of results.
This site can display upto 89 results.
Blood
|
January 1, 1988
Mild and severe beta-thalassemia among homozygotes from Turkey: identification of the types by hybridization of amplified DNA with synthetic probes
J C Diaz-Chico, K G Yang, T A Stoming, et al.
Hemoglobin
|
January 1, 1988
Some rare hemoglobin variants with altered oxygen affinities; Hb linkoping [beta 36(C2)Pro----Thr], Hb Caribbean [beta 91(F7)Leu----Arg], and Hb Sunnybrook [beta 36(C2)Pro----Arg]
M A Ali, P Pinkerton, S W Chow, 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-thalassemia
J M Gonzalez-Redondo, T A Stoming, A Kutlar, et al.
American Journal of Hematology
|
December 1, 1993
Hb Adana or alpha 2(59)(E8)Gly-->Asp beta 2, a severely unstable alpha 1-globin variant, observed in combination with the -(alpha)20.5 Kb alpha-thal-1 deletion in two Turkish patients
M A Cürük, A J Dimovski, E Baysal, et al.
Blood
|
May 1, 1990
Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions
J B Wilson, B B Webber, H Hu, et al.
American Journal of Hematology
|
March 1, 1993
Spleen in sickle cell anemia: comparative studies of Nigerian and U.S. patients
A D Adekile, K M McKie, O O Adeodu, et al.
Hemoglobin
|
January 1, 1988
Hb Las Palmas or alpha 2 beta 2(49)(CD8)Ser----Phe, a mildly unstable hemoglobin variant
J J Malcorra-Azpiazu, M I Balda-Aguirre, J C Diaz-Chico, et al.
Blood
|
September 1, 1988
Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States
J M Gonzalez-Redondo, T A Stoming, K D Lanclos, et al.
British Journal of Haematology
|
March 1, 1988
Variation in clinical severity among patients with Hb Lepore-Boston-beta-thalassaemia is related to the type of beta-thalassaemia
D G Efremov, G D Efremov, N Zisovski, et al.
Page
of 9