Within the last year
Within the past 3 years
1 - 8 of 8 articles
Three patients heterozygous for a partial deletion of the β-globin gene were studied: an American Black with an ≈1.35 kb deletion, a Turkish patient with an ≈300 nucleotide deletion, and a Greek patient with a newly discovered deletion of 44 nucleotides. The DNA was amplified by the...
The β-gene-cluster haplotype and α-gene status were determined for 221 patients with sickle cell anemia, 41 with SC disease, and 21 with S-β-thalassemia. Among SS patients, eleven β s haplotypes were found in 21 combinations. Three haplotypes — the Benin (Ben) (—+−), the Central African...
Suspensions of red cells containing Hb Marseille-Long Island showed decreased oxygen affinity and low interaction with 2,3-diphosphoglycerate. Oxygen equilibrium studies of the purified component confirmed these abnormalities. Oxidation rate measurements of carbonmonoxy-Hb Marseille and...
An abnormal profile of cation exchange high performance liquid chromatography for the determination of Hb A 1c led to the discovery of a new hemoglobin variant with a His→Tyr substitution at position 97(FG4) of the β chain. The variant comprised about equal proportion to normal Hb A. Lt showed...
Read and print from thousands of top scholarly journals.
Sign up with Facebook
Sign up with Google
Already have an account? Log in
Save this article to read later. You can see your Read Later on your DeepDyve homepage.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Sign Up Log In
To subscribe to email alerts, please log in first, or sign up for a DeepDyve account if you don’t already have one.
To get new article updates from a journal on your personalized homepage, please log in first, or sign up for a DeepDyve account if you don’t already have one.