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Blood|March 1, 1975
Hemoglobin J-Chicago (beta76(E20) Ala yields Asp): a new hemoglobin variant resulting from substitution of an external residueP L Romain, A D Schwartz, M Shamsuddin, et al.
The Journal of Clinical Investigation|December 1, 1991
Effects of alpha-thalassemia and sickle polymerization tendency on the urine-concentrating defect of individuals with sickle cell traitA K Gupta, K A Kirchner, R Nicholson, et al.
American Journal of Hematology|October 1, 1991
Hb S/beta zero-thalassemia due to the approximately 1.4-kb deletion is associated with a relatively mild phenotypeJ S Waye, D H Chui, B Eng, et al.
Nursing Administration Quarterly|June 11, 1999
How other members of the top management team see the nurse executiveR Wells, J A Alexander, M M Piotrowski, et al.
The American Journal of the Medical Sciences|August 1, 1992
Beta-thalassemia intermedia with exceptionally high hemoglobin A2: relationship to mutations in the beta-gene promoterM B Coleman, J G Adams, M W Plonczynski, et al.
American Journal of Hematology|February 1, 1993
G gamma A gamma (beta+) hereditary persistence of fetal hemoglobin: the G gamma -158 C-->T mutation in cis to the -175 T-->C mutation of the A gamma-globin gene results in increased G gamma-globin synthesisM B Coleman, J G Adams, M H Steinberg, et al.
The Journal of Clinical Investigation|July 1, 1981
Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys)E J Benz, B W Berman, B L Tonkonow, et al.
Blood|December 15, 1990
Molecular basis for alpha-thalassemia associated with the structural mutant hemoglobin Suan-Dok (alpha 2 109leu----arg)I Weiss, F E Cash, M B Coleman, et al.
American Journal of Hematology|March 1, 1995
Gender and haplotype effects upon hematological manifestations of adult sickle cell anemiaM H Steinberg, H Hsu, R L Nagel, et al.
Blood|June 1, 1984
Effects of thalassemia and microcytosis on the hematologic and vasoocclusive severity of sickle cell anemiaM H Steinberg, W Rosenstock, M B Coleman, et al.
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