A. Miller

The Structure of Goat Hemoglobins V. A Fourth β Chain Variant (β-D-Malta; 69 Asp ↠ Gly) with Decreased Oxygen Affinity and Occurring at a High Frequency in Malta

J. V. Bannister, T. Huisman, W. Bannister, 1979 .

THE PRESENT STATUS OF THE HETEROGENEITY OF FETAL HEMOGLOBIN IN β‐THALASSEMIA: AN ATTEMPT TO UNIFY SOME OBSERVATIONS IN THALASSEMIA AND RELATED CONDITIONS *

G. Apell, W. Schroeder, E. Rachmilewitz, 1974, Annals of the New York Academy of Sciences.

δβ ‐Thalassaemia in Two Yugoslavian Families

T. Huisman, W. Schroeder, G. Efremov, 2009 .

Interaction of the β chain variant hemoglobin leslie and the α chain variant hemoglobin montgomery in a black female

A. Felice, T. Huisman, A. Miller, 1980 .

Is the trimodality of Hb leslie (α2β2 131Gln → 0) in heterozygotes the result of a variable number of active α‐chain genes? Evidence for posttranslational control of hemoglobin synthesis

A. Felice, E. Abraham, T. Huisman, 1978 .

Sickle cell anemia and trait in Southern India: Further studies

G. Brittenham, B. Lozoff, T. Huisman, 1979, American journal of hematology.

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

A. Felice, T. Huisman, S. Mayson, 1979 .