H. F. Harris

A Search for Anomalies in the ζ,α,β, and γ Globin Gene Arrangements in Normal Black, Italian, Turkish, and Spanish Newborns

Y. J. Fei, F. Kutlar, H. F. Harris et al. · Hemoglobin · 1989 · 55 citations

Polymorphisms in the human haptoglobin gene cluster: chromosomes with multiple haptoglobin-related (Hpr) genes.

Nobuo Maeda, S M McEvoy, H. F. Harris et al. · Proceedings of the National Academy of Sciences · 1986 · 42 citations

Allelic Variant, Haplotype Determination, Linkage Disequilibrium +12

The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis

Alex E. Felice, B. B. Webber, A L Miller et al. · American Journal of Hematology · 1979 · 29 citations

Immunohematology, Iron Metabolism, Genetics +20

Hb A2-Wrens or α2δ298(FG5)Val → MEt, an unstable δ chain variant identified by sequence analysis of amplified DNA

John Codrington, F. Kutlar, H. F. Harris et al. · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · 1989 · 27 citations

Amplified Dna, Dna Sequencing, Natural Sciences +12

The Synthesis of Fetal Hemoglobin Types in red Blood Cells and in BFU-E Derived Colonies from Peripheral Blood of Patients with Sickle Cell Anemia, β⁺- and δβ-Thalassemia, Various forms of Hereditary Persistence of Fetal Hemoglobin, Normal Adults and Newborn

T. H. J. Huisman, A. L. Reese, John S. Howard et al. · Hemoglobin · 1979 · 21 citations