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American Journal of Hematology|March 1, 1991
Effect of beta-globin gene cluster haplotype on the hematological and clinical features of sickle cell anemiaR F Rieder, S Safaya, P Gillette, et al.
Blood|February 1, 1986
A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell traitM H Steinberg, M B Coleman, J G Adams, et al.
The Journal of Nursing Administration|April 14, 1999
Decision-making activity and influence of nurse executives in top management teamsJ Banaszak-Holl, J Alexander, N M Valentine, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1981
beta-Thalassemia present in cis to a new beta-chain structural variant, Hb Vicksburg [beta 75 (E19)Leu leads to 0]J G Adams, M H Steinberg, M V Newman, et al.
Journal of the American Veterinary Medical Association|March 1, 1994
Orotracheal and nasotracheal intubation in llamasT W Riebold, H N Engel, T L Grubb, et al.
The Journal of Clinical Investigation|May 1, 1979
Hemoglobin Indianapolis (beta 112[G14] arginine). An unstable beta-chain variant producing the phenotype of severe beta-thalassemiaJ G Adams, L A Boxer, R L Baehner, et al.
Blood|March 1, 1991
High hemoglobin A2 beta 0-thalassemia due to a 532-basepair deletion of the 5' beta-globin gene regionJ S Waye, S P Cai, B Eng, et al.
The Journal of Clinical Investigation|March 1, 1987
Hemoglobin Mississippi (beta 44ser----cys). Studies of the thalassemic phenotype in a mixed heterozygote with beta +-thalassemiaM H Steinberg, J G Adams, W T Morrison, et al.
Blood|February 1, 1983
Hemoglobin North Shore: a variant hemoglobin associated with the phenotype of beta-thalassemiaC M Smith, B Hedlund, J A Cich, et al.
The Journal of Clinical Investigation|February 1, 1995
Two missense mutations in the beta-globin gene can cause severe beta thalassemia. Hemoglobin Medicine Lake (beta 32[B14]leucine-->glutamine; 98 [FG5] valine-->methionine)M B Coleman, Z H Lu, C M Smith, et al.
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