Influence of hemoglobin S adducts on hemoglobin A2 quantification by HPLC

Clinical Chemistry

Volumn 42, Issue 7, 1996, Pages 1113-1114

  Suh, David D ^a   Krauss, Jonathan S ^a   Bures, Keith ^a  

^a MEDICAL COLLEGE OF GEORGIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

HEMOGLOBIN A2; HEMOGLOBIN C; HEMOGLOBIN DELTA CHAIN; HEMOGLOBIN S;

ACCURACY; ARTICLE; BETA THALASSEMIA; HEMOGLOBIN DETERMINATION; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; SICKLE CELL TRAIT;

EID: 0000606380     PISSN: 00099147     EISSN: None     Source Type: Journal    
DOI: 10.1093/clinchem/42.7.1113     Document Type: Article

References (7)

1. Rucknagel DL. The biochemical genetics of sickle cell anemia and related hemoglobinopathies. In: Levere RD, ed. Sickle cell anemia and other hemoglobinopathies. New York: Academic Press, 1975:13.
2. 2 in patients with AC trait, CC disease, and C-beta-thalassemia. Clin Chim Acta 1972;40:159-63.
3. 2 is higher in sickle cell trait than in normal homozygotes. Hemoglobin 1981;5:371-8.
4. 2 and F. J Clin Pathol 1993;46:852-6.
5. 2. J Lab Clin Med 1974;83:657-64.
6. Kutlar A, Kutlar F, Wilson JB, Headlee MG, Huisman THJ. Quantitation of hemoglobin components by high-performance cation-exchange liquid chromatography: its use in the diagnosis and in the assessment of cellular distribution of hemoglobin variants. Am J Hematol 1984;17:39-53.
7. Roa D, Turner EA, Aguinaga MdP. Reference ranges for hemoglobin variants by HPLC in African Americans. Ann Clin Lab Sci 1995;25:228-35.